Events

MiSeq i100 Series empowers new sequencing possibilities

Watch the unveiling of the MiSeq i100 Series in this webinar. Discover how it will accelerate insights and discoveries with faster, simpler sequencing.

Watch webinar

Webinar
Jan 2016 -
Keeping pace with immuno-oncology research breakthroughs and biomarker identification
PastWebinar
May 04
Keeping pace with immuno-oncology research breakthroughs and biomarker identification
May 4, 2016

The excitement surrounding immuno-oncology is being driven by results seen in the clinic. New treatments can potentially be made more efficacious using NGS technology that would accelerate biomarker identification and bring down costs for research subject screening and safety monitoring. Among these technologies is RNA-Seq, a flexible sequencing assay that enables multiple applications with one assay from a single sample. In this webinar, we'll summarize the clinical relevance of RNA-Seq, when and how to use expression profiling economically, some common challenges and associated remedies.

Key learning objectives
 
Learn how legacy RNA-Seq datasets can be revisited for new insights to keep pace with today’s rapid advance of therapeutic breakthroughs
Learn how RNA-Seq provides high-throughput, comprehensive, direct measurement of functionally relevant molecular processes
Learn more about key applications for RNA-Seq in immuno-oncology
Development and Validation of Automated Methods for Metagenomic Analyses
PastWebinar
Sep 06
Development and Validation of Automated Methods for Metagenomic Analyses
Sep 6, 2016
Automated methods for 16S rDNA amplicon and whole genome shotgun sequencing as well as discuss the impact of automation on quality.
Metagenomic Applications for Microbiome-Related Studies of Complex Disease
PastWebinar
Nov 01
Metagenomic Applications for Microbiome-Related Studies of Complex Disease
Nov 1, 2016
Advanced analyses of 16S rRNA gene, and bacterial/viral metagenomic data.
Emerging methods: Driving transcriptome and epigenetics discovery with RNA-Seq and Methyl-Seq
PastWebinar
Dec 08
Emerging methods: Driving transcriptome and epigenetics discovery with RNA-Seq and Methyl-Seq
Dec 8, 2016

As researchers seek to understand how the transcriptome shapes biology, RNA-Seq is
becoming recognized as one of the most significant and powerful tools in modern science. With RNA-Seq, researchers can detect the fine architecture of the transcriptome, such as transcript isoforms, gene fusions, single nucleotide variants, and other features—without prior knowledge. In addition to RNA-Seq, methylation sequencing can provide insights into the regulation of RNA and the temporal and spatial expression of gene products. By combining both RNA and methylation sequencing, researchers who study complex disease, cancer, and other biological systems will have a more complete picture of the transcriptome and its underlying regulatory features.

In this live webinar, we discuss the RNA-Seq and Methyl-Seq workflows that can help researchers drive breakthroughs and understanding in the area of gene expression and gene regulation. Join our gene expression and methylation experts as they review how researchers are driving discovery and learn how our workflows can help your lab leverage the power of next-generation sequencing.

CosmosID Metagenomics for Rapid Detection of Enteric Pathogens and Characterization of Antimicrobial Resistance in Health and Disease
PastWebinar
Dec 14
CosmosID Metagenomics for Rapid Detection of Enteric Pathogens and Characterization of Antimicrobial Resistance in Health and Disease
Dec 14, 2016
High throughput sequencing, combined with a high resolution bioinformatics platform, provides a powerful tool for researching enteric diseases and for agricultural and environmental applications.
See the NovaSeq Series in action
PastWebinar
Jan 24
See the NovaSeq Series in action
Jan 24, 2017

Discover a new era of sequencing with the NovaSeq Series. Join us for a live webinar event to see firsthand how we are redefining what is possible with high-throughput sequencing. Built from the ground up to fulfill your scientific visions, the NovaSeq Series gives you the flexibility and scalability to complete projects faster and more economically than ever before across a broad range of applications.

Webinar at a glance

  • Overview of instrument and consumables
  • Demonstration from run setup through data analysis
  • Data analysis using BaseSpace® Sequence Hub
Illumina TruSight HLA Case Study Webinar Series  HLA typing of buccal swabs using TruSight HLA
PastWebinar
Feb 15
Illumina TruSight HLA Case Study Webinar Series HLA typing of buccal swabs using TruSight HLA
Feb 15, 2017

The Webinar Series will feature HLA laboratory directors presenting case studies from samples prepared with TruSight HLA , sequenced with Illumina next-generation sequencing (NGS) MiSeq or MiniSeq systems, and analyzed using TruSight HLA Assign software.

The Human Microbiome: lessons and challenges in deciphering the microbiota in health and disease
PastWebinar
Apr 04
The Human Microbiome: lessons and challenges in deciphering the microbiota in health and disease
Apr 4, 2017
This talk will present the progress made in metagenomics and the use of largely unassembled sequences in constructing the microbial communities forming the human microbiome.
iDTECT Blood, a sample-to-report next-generation sequencing (NGS) solution for precision diagnostics in infectious diseases
PastWebinar
May 02
iDTECT Blood, a sample-to-report next-generation sequencing (NGS) solution for precision diagnostics in infectious diseases
May 2, 2017
This webinar will provide an overview of the development, validation and clinical evaluation of PathoQuest’s iDTECT Blood.
Dissecting the genetic basis of Brugada Syndrome
PastWebinar
May 23
Dissecting the genetic basis of Brugada Syndrome
May 23, 2017

Brugada Syndrome belongs to a family of rare inherited cardiac disorders that can lead to sudden cardiac death. Rare genetic variants in the SCN5A gene can be identified in ~20%* of cases with Brugada Syndrome, while the genetic basis in the others remains unresolved.

Ongoing studies, combining data from multiple genomic methods, are helping to elucidate the genetic basis of Brugada Syndrome and other complex cardiac disorders with the aim of improving patient care in the future.

Register for the webinar to hear Professor Connie Bezzina present data from her laboratory and ongoing collaborative studies with the Brugada Syndrome Genetics Consortium.

The Effective Implementation of NIPT into a Busy Practice: An Obstetrician Perspective
PastWebinar
Jun 27
The Effective Implementation of NIPT into a Busy Practice: An Obstetrician Perspective
Jun 27, 2017
In this webinar, Tina Ziainia, MD, FACOG, an Obstetrician-Gynecologist affiliated with Sharp HealthCare, provides insight and expertise on successfully implementing NIPT into a busy practice.
Next-generation solutions for the next era of sequencing
PastWebinar
Nov 14
Next-generation solutions for the next era of sequencing
Nov 14, 2017

The latest NovaSeq advancements have arrived—delivering unprecedented scalability and flexibility for next-generation sequencing (NGS). Discover how the S4 flow cell allows you to use the NovaSeq 6000 System to take your research to the next level.

Join Gary Schroth, Illumina Distinguished Scientist, to learn about these latest advancements with the NovaSeq 6000 System. See how the S4 can provide you the highest throughput of any sequencer. Finally, with the new NovaSeq Xp workflow, you can expand your research, giving you more flexibility than ever before.

Enabling efficient Discovery and Clinical Research in drug response: Application of a targeted Next-Generation Sequencing Assay for Pharmacogenetics
PastWebinar
Dec 07
Enabling efficient Discovery and Clinical Research in drug response: Application of a targeted Next-Generation Sequencing Assay for Pharmacogenetics
Dec 7, 2017
In this presentation, we will describe a method and workflow for targeted pharmacogenetic gene sequencing using Kailos’ TargetRich™ PGxComplete assay.
High-volume sequence analysis with BaseSpace Sequence Hub and Edico Genome DRAGEN apps
PastWebinar
Dec 13
High-volume sequence analysis with BaseSpace Sequence Hub and Edico Genome DRAGEN apps
Dec 13, 2017
In this webinar, we describe BaseSpace™ Sequence Hub and how the newest features support high throughput, high-volume sequencing.
AmpliSeq™ for Illumina®—fast, simple, robust targeted library prep chemistry for Illumina sequencing systems
PastWebinar
Jan 23
AmpliSeq™ for Illumina®—fast, simple, robust targeted library prep chemistry for Illumina sequencing systems
Jan 23, 2018

See what happens when a leading library prep is optimized to run on next-generation sequencing (NGS) systems from Illumina. Join Mitu Chaudhary and Claire White as they present data to demonstrate the robust performance of AmpliSeq for Illumina from a wide variety of sample types.

CosmosID Metagenomics for Public Health, Food/Water Safety, and Epidemiology
PastWebinar
Jan 24
CosmosID Metagenomics for Public Health, Food/Water Safety, and Epidemiology
Jan 24, 2018
Hear about how CosmosID has developed a cloud-based microbial genomics platform.
Introducing the iSeq™ 100 Sequencing System—our latest solution for fast and efficient low-throughput sequencing for virtually any lab
PastWebinar
Jan 30
Introducing the iSeq™ 100 Sequencing System—our latest solution for fast and efficient low-throughput sequencing for virtually any lab
Jan 30, 2018

Explore our smallest and most cost-effective sequencer ever. Join Bellal Moghis and Gary Schroth as they introduce our newest system—iSeq 100. They’ll walk through installation and also review applications and methods. Find out how you can make the most of your new lab partner.

Immunotherapy and genomics innovation advance Illumina’s vision for precision oncology
PastWebinar
Jul 20
Immunotherapy and genomics innovation advance Illumina’s vision for precision oncology
Jul 20, 2018

Genomics is facilitating a deeper understanding of cancer biology and through clinical research, new biomarkers are emerging that pave the way for next-generation therapeutics to help fight cancer in a more personalized way. 

In this webinar, Sandip Patel, MD will provide a review of biomarker research and discoveries in the field of Immunotherapy and Garret Hampton, PhD will discuss Illumina’s vision for Oncology and share how genomics will enable broader availability of comprehensive tumor sequencing to explore complex biomarkers and assess tumor mutational burden.

 

Human and Environmental Microbial Health: A Global Perspective
PastWebinar
Sep 12
Human and Environmental Microbial Health: A Global Perspective
Sep 12, 2018

Understanding the microbial ecosystem dynamics of our planet is central to our role as custodians of the planet. The Earth Microbiome Project aimed to characterize the microbial diversity of the diverse ecosystems across our world, which we have used to model the ecosystem dynamics of these environments. Integrating these models with agricultural policy provides a framework on which to determine how climate change and shifting policy will influence the microbial metabolic dynamics, which will affect our ability to modulate system scale outcomes. In concert with this global perspective we are also characterizing the human microbiome, which has become a key part of patient care, provide new avenues to diagnose and treat human disease. The immune system controls our interaction with the microbial world, and yet the microbial communities in our bodies are central to modulating the immune response. Changes in the human microbiome have substantial influence on atopy, neurological disorders, metabolic disorders, and a range of complex conditions and disease states. We will discuss evidence of these mechanisms of interaction and how we have started to disturb the delicate balance of the immune-microbe equilibrium, impacting the development and function of our immune systems. Central to this disturbance is the distance we have placed between our children and the microbial world, which has been demonstrated to have a substantial influence on their physiological, immunological, neurological and even endocrinological development. Applying new strategies to identify how the microbial ecosystem correlates with diseases states and treatment efficacy through Microbiome-Wide Association Studies (MWAS) is altering the trajectory of precision medicine, and providing a new framework for facilitating patient care. 

Jack Gilbert

Jack Gilbert is the Faculty Director of the Microbiome Center, a Professor in the Department of Surgery at the University of Chicago Medicine, Senior Scientist (Adjunct) at Marine Biological Laboratory, and Group Leader in Microbial Ecology at Argonne National Laboratory. Gilbert's research is focused on the ecology, evolution, and metabolic dynamics of microbial ecosystems from myriad environments including built environments, oceans, rivers, soils, air, plants, animals, and humans. His primary interest is in using omics technologies (metagenomics, metatranscriptomics, metabolomics) to capture longitudinal dynamics in microbial ecosystems and then model how these interactions relate the environmental variables, be those variables disease onset and immunology in humans or chemical transformations in plants and soils. Gilbert is developing unifying principles which govern how microbial communities assemble. He founded the Earth Microbiome Project, and co-founded the American Gut Project, and is the editor-in-chief of the journal mSystems.

Performing In-Depth Microbiome Analysis with the One Codex Bioinformatics Platform
PastWebinar
Oct 09
Performing In-Depth Microbiome Analysis with the One Codex Bioinformatics Platform
Oct 9, 2018

Microbiome research is quickly becoming one of the most exciting fields in the life sciences, driven by the power of next-generation sequencing (NGS). One Codex is a leading platform for rapid, accurate microbiome and metagenomics analysis and is used by researchers across major academic, commercial, and clinical institutions. In this webinar, we will walk through a gut microbiome experiment including sample collection, sequencing, bioinformatics, and analysis.

On the bioinformatics side, we will show how you can easily analyze NGS datasets with the One Codex database of >80,000 whole microbial genomes. We will review several types of microbiome analyses from taxonomic classification to building predictive machine learning models. Finally, we will demonstrate how it can all be performed in a scalable, repeatable fashion, ensuring that your microbiome research is reproducible whether it involves 10 samples or 10,000.

Precision Metagenomics to Identify Patients at Risk for Invasive Infection
PastWebinar
Dec 10
Precision Metagenomics to Identify Patients at Risk for Invasive Infection
Dec 10, 2018

This webinar discusses the use of shotgun metagenomics to identify children at risk of hospital-acquired infection.

Our speaker, David Haslam of Cincinnati Children's Hospital, details methods used to eradicate colonization with pathogenic organisms and hopefully prevent bloodstream infections. He also discusses how bacterial whole genome sequencing and shotgun metagenomics can be used to track and prevent transmission of hospital-acquired infections.

Dr. Haslam shares how this work fits within his lab's goal of identifying risk factors for invasive infection due to multidrug resistant bacteria. His team is applying next generation sequencing and metagenomic analysis to identify changes in the microbiome that correlate with risk for invasive infection and is currently developing this assay into a clinically actionable test.

Illumina DNA Prep: A Robust and Self-Normalizing Enzymatic Library Prep Technology
PastWebinar
Jan 30
Illumina DNA Prep: A Robust and Self-Normalizing Enzymatic Library Prep Technology
Jan 30, 2019
Illumina DNA Prep is a novel bead-linked-transposome technology, which addresses these shortcomings whilst retaining the convenience of enzymatic fragmentation.
Introducing Illumina DNA Prep with Enrichment (formerly Nextera Flex for Enrichment)
PastWebinar
Feb 20
Introducing Illumina DNA Prep with Enrichment (formerly Nextera Flex for Enrichment)
Feb 20, 2019
Illumina DNA Prep with Enrichment (formerly Nextera Flex for Enrichment) is the fastest and most flexible targeted sequencing solution for DNA in the Illumina library prep portfolio.
Comprehensive NTRK Fusion Detection, Agnostic of the Fusion Partner, for Optimal Identification of Rare Genomic Events
PastWebinar
Feb 27
Comprehensive NTRK Fusion Detection, Agnostic of the Fusion Partner, for Optimal Identification of Rare Genomic Events
Feb 27, 2019
NTRK fusions are rare but important recent biomarkers linked to response to new TRK inhibitors. Comprehensive genomic profiling on all solid tumors permits detection of rare genomic events and in the future may enables the use of emerging treatments such as NTRK inhibitors. NTRK genes include numerous potential fusion partners, large intronic regions and G-C rich content, making accurate and comprehensive detection of NTRK fusions difficult to perform in the lab. Amongst the variable performance of NTRK fusion assays, NTRK detection from RNA using Hybrid-Capture NGS provides comprehensive and accurate fusion detection, agnostic of the fusion partner.
Delivering New Capabilities on Illumina Sequencers, from iSeq™ to NovaSeq™
PastWebinar
Feb 28
Delivering New Capabilities on Illumina Sequencers, from iSeq™ to NovaSeq™
Feb 28, 2019

See what new product developments are available in the Illumina sequencing portfolio.  Join David Miller from Illumina Product Marketing, as he presents data in support of new software, robust sequencing kit performance, and longer reads on a variety of next-generation sequencing (NGS) systems from Illumina.

Library Prep Innovation Pipeline at Illumina: Targeted DNA, RNA & Epigenetics
PastWebinar
Mar 01
Library Prep Innovation Pipeline at Illumina: Targeted DNA, RNA & Epigenetics
Mar 1, 2019

Illumina product development presents the next era of library prep.  The new Nextera™ DNA Flex and Nextera™ DNA Flex for Enrichment library prep solutions deliver consistent insert sizes, uniform coverage, optimized performance, and highly reproducible data across all Illumina sequencing systems.  This bead-based technology minimizes bias and opportunities for error, resulting in highly reproducible sequencing data. 

HiSeq™, NovaSeq™, and iSeq™: Project Transitions to Leverage Larger Scale Sequencing
PastWebinar
Mar 02
HiSeq™, NovaSeq™, and iSeq™: Project Transitions to Leverage Larger Scale Sequencing
Mar 2, 2019

The latest sequencing technologies enable unprecedented throughput and redefine limits for many labs.  Join Shawn Levy, Faculty Investigator at the HudsonAlpha Institute for Biotechnology, as he presents data demonstrating how multiple Illumina sequencing systems can be utilized together in a lab setting to facilitate larger scale sequencing.

Delivering More Than Data: Informatics solutions for NGS with DRAGEN™ and BaseSpace™
PastWebinar
Mar 02
Delivering More Than Data: Informatics solutions for NGS with DRAGEN™ and BaseSpace™
Mar 2, 2019

Data volumes are growing more rapidly than ever before.  Join Menzies Chen, Illumina Product Manager, as he discusses the newest informatics features to support high throughput, high volume sequencing.  With DRAGEN™ technology, bioinformatics workflows can now be run on specialized hardware to accelerate the speed of analysis.

Transforming the Future of Genomics Together / HiSeq™, NovaSeq™, and iSeq™: Project Transitions to Leverage Larger Scale Sequencing
PastWebinar
Mar 02
Transforming the Future of Genomics Together / HiSeq™, NovaSeq™, and iSeq™: Project Transitions to Leverage Larger Scale Sequencing
Mar 2, 2019

Part 1: Transforming the Future of Genomics Together, with Gary Schroth, Distinguished Scientist, Illumina, Inc.

Learn about the most recent product developments from Illumina in library preparation, next-generation sequencing (NGS) systems, and informatics.  Illumina Distinguished Scientist, Gary Schroth, presents a short overview on the newest in end to end next-generation sequencing (NGS) solutions as well as exciting new options for the future.

Part 2: HiSeq™, NovaSeq™, and iSeq™: Project Transitions to Leverage Larger Scale Sequencing, with Shawn Levy, Director of the HudsonAlpha Institute for Biotechnology

The latest sequencing technologies enable unprecedented throughput and redefine limits for many labs.  Join Shawn Levy, Faculty Investigator at the HudsonAlpha Institute for Biotechnology, as he presents data demonstrating how multiple Illumina sequencing systems can be utilized together in a lab setting to facilitate larger scale sequencing.

Transforming the Future of Genomics Together
PastWebinar
Mar 02
Transforming the Future of Genomics Together
Mar 2, 2019
Illumina Distinguished Scientist, Gary Schroth, presents a short overview on the newest in end to end next-generation sequencing (NGS) solutions at AGBT 2019.
New Methods for Old Problems: Using Immunogenomics to Decode the Anti-Tumor T-Cell Repertoire
PastWebinar
Apr 02
New Methods for Old Problems: Using Immunogenomics to Decode the Anti-Tumor T-Cell Repertoire
Apr 2, 2019

Cancer arises due to an accumulation of genetic alterations, which can lead to the production of mutant proteins not expressed in normal cells, allowing recognition by the immune system. Kellie Smith, PhD, Assistant Professor of Oncology at Johns Hopkins University School of Medicine, presents her research on understanding the interplay of cancer neoantigens with the immune response at Illumina Exhibitor Spotlight Theater presentation at AACR 2019.

Best Practices for Implementing NGS and Positioning for Future Growth
PastWebinar
Apr 10
Best Practices for Implementing NGS and Positioning for Future Growth
Apr 10, 2019
A community based cancer medical center provides perspectives on why they chose to internalize NGS testing.
Envisioning the Future of Pathology in Precision Oncology
PastWebinar
Apr 10
Envisioning the Future of Pathology in Precision Oncology
Apr 10, 2019
A representative from a regional reference lab provides his perspectives on why they chose to internalize NGS testing,
Neoantigen Discovery: Realizing the Promise of Personalized Treatment
PastWebinar
Apr 18
Neoantigen Discovery: Realizing the Promise of Personalized Treatment
Apr 18, 2019

Advances in next-generation sequencing technology and computational data analysis have revolutionized efforts to identify tumor-specific mutant antigens. These altered, potentially immunogenic proteins may prove to be an important target for immunotherapies. In this Cell Press Webinar, Nicholas McGranahan (University College London) and Gerald Linette (University of Pennsylvania) will review progress made and future applications of this important area of cancer immunogenomics.

Virus-Specific Target Capture Coupled with NGS for Rapid and Sensitive Respiratory Virus Detection
PastWebinar
May 01
Virus-Specific Target Capture Coupled with NGS for Rapid and Sensitive Respiratory Virus Detection
May 1, 2019

This webinar will discuss the benefits of virus-specific target capture combined with next-generation sequencing (NGS) to identify viral infections and conduct comprehensive genomic and transcriptomic interrogation.

The high diversity of inter-virus genome types and intra-virus genomic heterogeneity, together with the complexity of sample types, make NGS-based clinical virology difficult, arduous, and expensive. A single method that is able to use nucleic acids that are of low quantity and poor quality to examine both DNA and RNA viruses from a mixed cell population that may include human, bacteria, and viruses would be ideal.   

To this end, our speaker, Darrell L. Dinwiddie of the University of New Mexico Health Sciences Center, will discuss a method his team has been evaluating that uses virus-specific target capture probe sets coupled with NGS.

Dr. Dinwiddie will discuss how this method has demonstrated significant improvement in respiratory viral identification and genome coverage compared to unenriched NGS. His team has shown the ability to effectively capture and sequence viruses that may differ from the probes by as much as 10 percent to 15 percent. These methods have worked for viral sequencing from purified viral stocks, in vitro cell culture, and clinical samples.

This webinar will also address the broader implications of this work, including surveillance, epidemiologic studies, and public health planning.

For example, in two hospital outbreak studies, Dr. Dinwiddie and colleagues have shown that target capture and NGS enabled sensitive discrimination of the relatedness of respiratory syncytial virus and human parainfluenza virus 3 isolates obtained during the outbreak and provided evidence for source of transmission.

In addition, through multi-year retrospective and prospective NGS studies of respiratory viral infections at multiple pediatric hospitals, Dr. Dinwiddie and his team have been able to examine seasonal respiratory virus genomic variation, evolution, and distribution for several respiratory viruses. This includes evaluating the match of vaccine to circulating influenza virus strains and the correlation between virus strains and clinical severity of infections.  The recently developed Human Pan Viral sequencing methods by Illumina and Twist Biosciences will enable similar studies not only for respiratory viruses, but for all types of human viral pathogens across all sample types of interest. 

Darrell L. Dinwiddie, PhD
Assistant Professor, Department of Pediatrics
Scholar, Clinical Translational Science Center
University of New Mexico Health Sciences Center

Quantifying immune contexture in human tumors using RNA-Seq
PastWebinar
May 08
Quantifying immune contexture in human tumors using RNA-Seq
May 8, 2019

Watch this presentation to hear more about a novel approach that uses hybrid avatars and perturbation biology. The idea is to use complementary data to extract immunologically relevant information.

By combining the analysis of RNA sequencing and image data, Prof. Zlatko Trajanoski’s lab in Innsbruck has devised a powerful workflow that will enable precision immuno-oncology.

Accelerating Crop Research with High-Quality Affordable Genome Assemblies
PastWebinar
Jun 06
Accelerating Crop Research with High-Quality Affordable Genome Assemblies
Jun 6, 2019
In this webinar, Assaf Distelfeld from Tel Aviv University, a world leader in wheat genomic research, discusses recently generated genome assemblies of wheat progenitors, and how this new resource can help solve biological questions and improve wheat breeding. In addition, representatives of NRGene, Illumina, and the University of Illinois at Urbana Champaign detail how their technology and services helped make this project happen, and others like it. The recent decrease in short-read sequencing costs and increased read lengths on the Illumina Novaseq sequencer and SP flow-cell, combined with NRGene’s accumulated experience in wheat genomics and bioinformatics, resulted in a more than 50 percent reduction in project cost. These innovations make de novo sequencing more accessible and affordable for researchers than ever before, without compromising genome assembly quality.
Personal and Clinical Utility of Polygenic Risk Scores:
PastWebinar
Jun 17
Personal and Clinical Utility of Polygenic Risk Scores:
Jun 17, 2019
This webinar provides an overview of polygenic risk scores, which aggregate dozens of genetic variants that have been linked to disease risk in genome-wide association studies (GWAS) into a single score.
Multiomics analyses: Why are they needed?
PastWebinar
Jun 24
Multiomics analyses: Why are they needed?
Jun 24, 2019
Discuss how approaches for epigenetics analyses and other omics can be used and integrated to examine different levels of genome activity in tissues and cells.
New Paradigms in Neuro-Oncology and Sarcoma Powered by DNA Methylation Classifiers
PastWebinar
Aug 13
New Paradigms in Neuro-Oncology and Sarcoma Powered by DNA Methylation Classifiers
Aug 13, 2019
This webinar discusses an approach that uses machine learning and epigenetic signatures to more effectively diagnose brain tumors.
Genomic Insights into Diversity: Population Scale Analysis
PastWebinar
Oct 16
Genomic Insights into Diversity: Population Scale Analysis
Oct 16, 2019
Report on the "All of Us" research program and Illumina’s new Global Diversity Array
Converting GWAS Signals to Effector Genes: Capture C Based Variant to Gene Mapping
PastWebinar
Oct 17
Converting GWAS Signals to Effector Genes: Capture C Based Variant to Gene Mapping
Oct 17, 2019
Learn more about a Capture C based approach that Grant’s team used to address pediatric loci associated with bone mineral density.
Accelerating Scientific Breakthroughs
PastWebinar
Oct 17
Accelerating Scientific Breakthroughs
Oct 17, 2019
Learn about new and upcoming product releases in library prep, sequencing, and informatics from Illumina Research and Development
Genome to Phenome: A New USDA Blueprint for Animal Genome Research
PastWebinar
Oct 22
Genome to Phenome: A New USDA Blueprint for Animal Genome Research
Oct 22, 2019
This webinar discusses a plan from the US Department of Agriculture to integrate animal genomics technologies into mainstream agricultural production strategies.
Next-Generation Sequencing Applications for the Clinical Microbiology Laboratory
PastWebinar
Oct 23
Next-Generation Sequencing Applications for the Clinical Microbiology Laboratory
Oct 23, 2019
Next Generation Sequencing (NGS) provides a molecular approach equivalent to culture and sensitivity testing for the clinical microbiology lab
Cancer Genomics: Deciphering Risk and Driving Discovery
PastWebinar
Oct 29
Cancer Genomics: Deciphering Risk and Driving Discovery
Oct 29, 2019
In this AJHG-Cell Press Webinar, Stephen Chanock (National Cancer Institute), Kate Nathanson (University of Pennsylvania), and Peter Campbell (Wellcome Sanger Institute), will explore the ways in which genomic technology has transformed cancer research, leading to new biological insights and revolutionizing clinical practice.
New Oncology Menu: Enhanced Capabilities to enable Comprehensive Genomic Profiling
PastWebinar
Nov 06
New Oncology Menu: Enhanced Capabilities to enable Comprehensive Genomic Profiling
Nov 6, 2019
In this webinar, taken from a live presentation given at AMP 2019, Dr. Biswajit Das of the Frederick National Laboratory (FNL)/MoCHA and Dr. Stephanie Hastings of Q2 Solutions, discuss their validation studies of the TruSight™ Oncology 500 ctDNA assay.
Comprehensive Genomic Profiling is Becoming a New Standard of Care in Oncology
PastWebinar
Nov 07
Comprehensive Genomic Profiling is Becoming a New Standard of Care in Oncology
Nov 7, 2019
Learn more about the benefits of broad biomarker detection with comprehensive genomic profiling (CGP).
Stakeholder Perspectives on Molecular Medicine: A Panel Discussion
PastWebinar
Nov 07
Stakeholder Perspectives on Molecular Medicine: A Panel Discussion
Nov 7, 2019
Oncologists and pathologists discuss comprehensive genomic profiling in cancer diagnosis and treatment.
Cancer at Single-Cell Resolution
PastWebinar
Nov 12
Cancer at Single-Cell Resolution
Nov 12, 2019
Leading researchers discuss how advances in Single-cell approaches can help unravel some of the deepest questions in cancer biology.
eRD GWAS: Unlocking Gene Expression as a Tool for Trait Mapping in Crops
PastWebinar
Nov 19
eRD GWAS: Unlocking Gene Expression as a Tool for Trait Mapping in Crops
Nov 19, 2019
In this webinar, Iowa State's Patrick Schnable will share details of eRD-GWAS and discuss a study that used the approach in maize.
Emerging Biomarkers in Thyroid Cancer and NSCLC
PastWebinar
Dec 09
Emerging Biomarkers in Thyroid Cancer and NSCLC
Dec 9, 2019
This webinar discusses emerging biomarkers for thyroid cancer and non-small cell lung cancer, with a particular focus on detecting gene fusions such as RET.
Can incorporation of genetic testing improve cardiovascular outcomes?
PastWebinar
Dec 12
Can incorporation of genetic testing improve cardiovascular outcomes?
Dec 12, 2019
Dr. Joshua Knowles will discuss both monogenic and polygenic forms of the familial hypercholesteremia (FH) phenotypes and the importance of genetic cascade testing using monogenic testing as well as Polygenic Risk Scores (PRS) in FH.
Polygenic risk scoring for common complex disease
PastWebinar
Dec 12
Polygenic risk scoring for common complex disease
Dec 12, 2019
Join Dr. Estelle Giraud as she provides an overview on Polygenic Risk Scores (PRS), why they are clinically relevant and how they may be used in the future.
What are polygenic risk scores and why are they important?
PastWebinar
Dec 12
What are polygenic risk scores and why are they important?
Dec 12, 2019
Dr. Leo Sugrue will explain Polygenic Risk Scores (PRS), how PRS can empower neuroimaging and importance of PRS in the identification of molecular mechanisms in neurological disease.
What are polygenic risk scores and why are they important?
PastWebinar
Dec 12
What are polygenic risk scores and why are they important?
Dec 12, 2019
Dr. Leo Sugrue will explain Polygenic Risk Scores (PRS), how PRS can empower neuroimaging and importance of PRS in the identification of molecular mechanisms in neurological disease.
Optimizing Cluster Density
PastWebinar
Feb 03
Optimizing Cluster Density
Feb 3, 2020
This webinar will cover critical parameters for optimizing cluster density on both our patterned and non-patterned flow cells. We will cover the following topics: factors that impact cluster efficiency; review of the clusters passing filter metric; how to diagnose clustering issues; and tips and tricks to achieve optimal density across our varying sequencing platforms.
Infinium Assay and GenomeStudio Genotyping: Introduction
PastWebinar
Feb 12
Infinium Assay and GenomeStudio Genotyping: Introduction
Feb 12, 2020
The Infinium assay is designed to interrogate many single nucleotide polymorphisms (SNPs) at extensive levels of loci multiplexing. GenomeStudio is a powerful solution that supports the genotyping analysis of microarray data. We will cover Infinium assay chemistry and the overview of Genotyping module on GenomeStudio. There will also be a basic workflow from project creation to report generation.
NextSeq™ 2000
PastWebinar
Feb 24
NextSeq™ 2000
Feb 24, 2020
Kieren Patel, NextSeq 2000 Product Manager, shares the latest in technology and system development from Illumina.
Illumina Software and Informatics Update
PastWebinar
Feb 25
Illumina Software and Informatics Update
Feb 25, 2020
Learn about new and upcoming product releases in informatics solutions from Illumina Software Engineering.
Enabling Next-Gen Workflows
PastWebinar
Feb 25
Enabling Next-Gen Workflows
Feb 25, 2020
Explore the latest advancements in next-generation sequencing technology with the NextSeqTM 2000. Hear Illumina VP, Ashley Van Zeeland, discuss end-to-end workflows on this scalable benchtop platform for a variety of emerging genomics applications.
AGBT Silver Sponsorship Workshop
PastWebinar
Feb 25
AGBT Silver Sponsorship Workshop
Feb 25, 2020
Join Illumina Distinguished Scientist, Gary Schroth as he provides a historical overview of the Illumina product pipeline and goes on to discuss the latest in Illumina partnerships and product releases first announced at the 2020 J.P. Morgan conference.
Library Prep Innovation Pipeline at Illumina
PastWebinar
Feb 25
Library Prep Innovation Pipeline at Illumina
Feb 25, 2020
Join Bellal Moghis, Product Manager at Illumina, as he discusses new technologies to offer users novel, easy-to-use, fast, and simple solutions for both DNA and RNA library preparation.
Next-Generation Sequencing in Clinical Molecular Diagnostics - The Crest and Trough
PastWebinar
Feb 26
Next-Generation Sequencing in Clinical Molecular Diagnostics - The Crest and Trough
Feb 26, 2020
The crest and trough of NGS as the title suggest describes the problem and pitfalls faced in a routine molecular diagnostic laboratory, the challenges in detection, identification and characterization of the molecular alterations which are clinically relevant. The classification of the alteration as per the recommended guidelines and the importance of the same has been discussed in this presentation. Overall, the study describes the incorporation of targeted gene panel in solid tumors into routine clinical practice.
Introduction to Beeline 2.0 Software and Array Analysis Workflows
PastWebinar
Feb 28
Introduction to Beeline 2.0 Software and Array Analysis Workflows
Feb 28, 2020
This webinar will cover critical parameters for optimizing cluster density on both our patterned and non-patterned flow cells. We will cover the following topics: factors that impact cluster efficiency; review of the clusters passing filter metric; how to diagnose clustering issues; and tips and tricks to achieve optimal density across our varying sequencing platforms.
Methylation analysis with Illumina - microarrays and NGS sequencing
PastWebinar
Mar 03
Methylation analysis with Illumina - microarrays and NGS sequencing
Mar 3, 2020
DNA methylation analysis can help researchers gain valuable insight into gene regulation and identify potential biomarkers. In this webinar, we will be discussing the Illumina portfolio of array-based and next-generation sequencing (NGS) analysis tools that provide robust, simple-to-use, and cost-efficient solutions for studying these epigenetic modifications and their impact on gene regulation.
TruSight Oncology 500 ctDNA pre-released version: Pan-Cancer Liquid Biopsy Assay
PastWebinar
Mar 10
TruSight Oncology 500 ctDNA pre-released version: Pan-Cancer Liquid Biopsy Assay
Mar 10, 2020
Learn more about implementing the TruSight Oncology 500 ctDNA assay to enable comprehensive genomic profiling (CGP) from circulating tumor DNA in this seminar recorded at AMP 2019. Dr. Biswajit Das of the Frederick National Laboratory (FNL)/MoCHA and Dr. Stephanie Hastings of Q2Solutions discuss their analytical validation studies using a pre-released version of TruSight Oncology 500 ctDNA assay in liquid biopsy samples.
Unraveling Cell Function Using Single-Cell Technologies
PastWebinar
Mar 19
Unraveling Cell Function Using Single-Cell Technologies
Mar 19, 2020
Kristy Red-Horse and Samantha Morris discuss how single-cell approaches can help advance our understanding of cell identity, development, and function.
The Peter Mac Experience with Comprehensive Genomic Profiling - The New Standard of Care in Tissue Pathology
PastWebinar
Apr 01
The Peter Mac Experience with Comprehensive Genomic Profiling - The New Standard of Care in Tissue Pathology
Apr 1, 2020
Listen to the Peter Mac’s Pathology Department share their experience in providing CGP in the translation research setting for personalised medicine trials. Characterising tumours using a comprehensive in-house clinical research panel provides useful diagnostic and predictive information that impacts patient care, however at relatively high per sample cost. Understand how they worked withh one of the first kit-based CGP research products meeting the Australian requirements for routine CGP.
Genomic Selection and SNP Genotyping in Crops and Livestock
PastWebinar
Apr 01
Genomic Selection and SNP Genotyping in Crops and Livestock
Apr 1, 2020
Food production is facing many challenges. Globally, we're seeing a big increase in food demand. Crops get lost to disease and we are overusing our planet's natural resources. We are in need of a system that will allow us to produce more with less. Can genomics help us deliver on the promise of a second green revolution? Can it help us answer the need of our generations and generations to come?
Introduction to GenomeStudio
PastWebinar
Apr 08
Introduction to GenomeStudio
Apr 8, 2020
Join this webinar to learn how to utilise GenomeStudio to perform analysis of Genotyping arrays. This webinar includes topics such as software download, installation, project creation and genotyping module capabilities and basic analysis workflow. The information is targeted to new Infinium genotyping array users. The webinar will be followed by a Q&A session
iSeq™ 100 System Introduction and 16S Metagenomics
PastWebinar
Apr 22
iSeq™ 100 System Introduction and 16S Metagenomics
Apr 22, 2020
Illumina Technical Support invites you to join us for a discussion of the new iSeq 100 system. This webinar is targeted to new users with a basic understanding of the Illumina sequencing workflow. This webinar will cover: Features of iSeq 100, end-to-end workflow, the new Illumina technologies that power the iSeq 100. And This webinar will cover 16S Metagenomics experiment and analysis topics by using iSeq 100 system. * Please note that this webinar will be conducted in Korean language.
Brain cartography: Building a map to navigate through target identification and validation
PastWebinar
Apr 24
Brain cartography: Building a map to navigate through target identification and validation
Apr 24, 2020
Dr. Mina Ryten explains how the rise of data accessibility around transcriptomics and epigenomics is driving methodologies leading to the improvement of genome annotation.
NextSeq 500/550 Run Quality and Troubleshooting
PastWebinar
Apr 24
NextSeq 500/550 Run Quality and Troubleshooting
Apr 24, 2020
Please join us for a presentation on evaluating the quality of data produced by NextSeq 500/550 runs and best practices to improve and achieve ideal data output. This webinar is targeted to new users of the NextSeq 500/550 so to familiarize them with reviewing problem phenotypes and the underlying causes.
Empowering Single Cell and Spatial Experiments with Sample Multiplexing
PastWebinar
Apr 28
Empowering Single Cell and Spatial Experiments with Sample Multiplexing
Apr 28, 2020
Customers will learn how using sample tagging with their single cell experiments can reduce library prep costs and increase flexibility.
The Genomic Landscape and Tumor Heterogeneity of Lung Adenocarcinoma in East Asia
PastWebinar
Apr 29
The Genomic Landscape and Tumor Heterogeneity of Lung Adenocarcinoma in East Asia
Apr 29, 2020
Lung cancer is the world’s leading cause of cancer death and shows strong ancestry disparities. Using genomic and transcriptomic sequencing across many patients as well as multiple sectors from multiple tumors, we characterized the genomic landscape of lung adenocarcinoma (LUAD) in East Asians (EAS). In this talk, we will elucidate a comprehensive genomic landscape of EAS LUADs and highlight important ancestry differences between patients from Asian and European Ancestry.
The Rise of Genome Interpretation
PastWebinar
May 05
The Rise of Genome Interpretation
May 5, 2020
Join Dr. Amit V. Khera as he provides a comprehensive overview of how understanding both rare and common genetic variation can be used as a tool to better understand disease biology and improve clinical care in cardiovascular disease as well as other important diseases.
NextSeq 2000: Exploring the End to End Workflows Enabled by Illumina’s Newest Sequencing System
PastWebinar
May 07
NextSeq 2000: Exploring the End to End Workflows Enabled by Illumina’s Newest Sequencing System
May 7, 2020
Learn more about Illumina’s newest platform and see performance data for exome sequencing, single-cell profiling, and transcriptome sequencing.
eRD GWAS: Unlocking Gene Expression as a Tool for Trait Mapping in Crops
PastWebinar
May 10
eRD GWAS: Unlocking Gene Expression as a Tool for Trait Mapping in Crops
May 10, 2020
eRD-GWAS, or "expression read depth genome-wide association study," is a genome-wide approach for identifying associations between variation in gene expression and variation in phenotypic traits. In this webinar, Dr. Patrick Schnable, from Iowa State University, will share details of this new method and discuss a study that used the approach in maize. Join us for this on-demand webinar to learn more.
Integrating Imaging and Sequencing Data to Understand Diseases in Single Cells and Tissues
PastWebinar
May 13
Integrating Imaging and Sequencing Data to Understand Diseases in Single Cells and Tissues
May 13, 2020
Spatial transcriptomics (ST) is emerging as the ‘next-generation’ single-cell RNA sequencing technology, as it adds an important spatial dimension to the transcriptome-wide gene expression data for cells within an intact tissue. From the same tissue section, ST generates three datatypes, including tissue-morphology, spatial location, and gene expression data. We hypothesise that integrating all three multimodal datatypes improves the accuracy and sensitivity in identifying cell types, cell-cell interactions and their interconnected transcriptional regulation within a physiologically intact tissue.
RNA Sequencing: Part II – Library Preparation kits and Best Handling Practices
PastWebinar
May 13
RNA Sequencing: Part II – Library Preparation kits and Best Handling Practices
May 13, 2020
Continuing on from Zena’s last webinar on RNA seq, this webinar will discuss best practices for Illumina’s TruSeq RNA kits, this webinar will review sample preparation kit options for total, mRNA and targeted RNA sequencing projects and then will focus on TruSeq RNA v2, TruSeq Stranded mRNA, and TruSeq Stranded Total RNA discussing best practices of bead handling, quantification methods, library QC, and troubleshooting. We assume a basic understanding of Illumina sequencing technology, but no prior knowledge of RNA sequencing is required. This webinar is aimed at both new and experienced users with a basic understanding of Illumina Sequencing technology and workflow.
NGS Applications for Infectious Disease
PastWebinar
May 28
NGS Applications for Infectious Disease
May 28, 2020
In this webinar, Kenny will talk about an overview of NGS application in Infectious disease field with comprehensive workflow include sample type dependent application such as shotgun metagenome, target enrichment and target amplification for viruses and bacteria. He also will explain how NGS is effectively utilized in this field, including the case study of COVID19. * Please note that this webinar will be conducted in Korean language.
Newborn Genomic Screening: In Sickness and In Health
PastWebinar
Jun 02
Newborn Genomic Screening: In Sickness and In Health
Jun 2, 2020
Learn about pioneering work in the field of newborn genome sequencing and analysis.
DRAGEN BioIT Platform Deep Dive on Capabilities and Technology.
PastWebinar
Jun 03
DRAGEN BioIT Platform Deep Dive on Capabilities and Technology.
Jun 3, 2020
Please join us for a deep dive on the DRAGEN BioIT platform. In this webinar, we will deep dive in the technology that makes DRAGEN, the different deployment methods of DRAGEN and the flexibility it offers. We will share DRAGEN’s latest pipeline roadmap, and some of examples of the many large key customer deployments and how they use DRAGEN. We will dive into the accuracy of some pipelines. Last, we will showcase the latest DRAGEN pipelines built to support Covid-19 detection, screening and surveillance.
Genomics' Role in Global COVID-19 Surveillance
PastWebinar
Jun 09
Genomics' Role in Global COVID-19 Surveillance
Jun 9, 2020
Join us and our global audience of change-makers, thought leaders and industry shapers for this enlightening discussion. This webcast is more relevant than ever before – because the very existence of COVID-19 magnifies the importance of meaningful dialogues such as this one.​
Enabling Scalable Comprehensive Genomic Profiling from FFPE Samples
PastWebinar
Jun 09
Enabling Scalable Comprehensive Genomic Profiling from FFPE Samples
Jun 9, 2020
Dr. Brian Piening of Providence Cancer Center will discuss why his team decided to implement in-house CGP and will share analytical performance data from their TSO500_HT runs.
Enabling High Resolution Spatial Profiling with Next Generation Sequencing
PastWebinar
Jun 10
Enabling High Resolution Spatial Profiling with Next Generation Sequencing
Jun 10, 2020
지금까지 대부분의 유전자 발현 연구는 상대 정량 PCR, 마이크로어레이, 차세대 염기서열분석(NGS)과 같은 다양한 방법을 이용해 하나의 시료에서 얻은 다수의 세포로 구성된 대용량의 시료를 분석하는 방식으로 진행되어 왔습니다. 하나의 동일한 시료임에도 불구하고 이질성을 보이는 세포들의 단일 세포 전사체를 분석한 NGS 데이터의 양이 최근 들어 폭발적으로 증가하는 것이 관찰되었습니다. 공간적 전사체학(spatial transcriptomics)은 일반 조직학 슬라이드에서 조직 샘플의 특정 영역에 대한 유전자 발현 프로파일을 찾아낼 수 있도록 해주어 미시환경적 차이(micro-environmental difference)에 관한 통찰력을 제시합니다. 이러한 대용량, 고해상도 방법이 가능한 이유는 NGS가 고품질의 다운스트림 분석용 데이터를 제공하기 위해 다양한 최적화된 표준(gold standard) 염기서열분석 장비와 널리 알려진 염기서열분석 기법을 채택하고 있기 때문입니다. 오늘 저희는 여러분의 공간적 전사체학 실험 계획과 기기 선택에 유용한 지침을 제공하고 최신 염기서열 기술에 대한 정보를 공유하고자 합니다. * This webinar is conducted in Korean language and hosted by Illumina in collaboration with NanoString Technologies.
Genomic Selection for Cattle and Buffaloes under Smallholder Production Systems in India
PastWebinar
Jun 10
Genomic Selection for Cattle and Buffaloes under Smallholder Production Systems in India
Jun 10, 2020
Learn more about how the customized genotyping chips - “INDUSCHIP” for cattle breeds and “BUFFCHIP” for buffalo breeds – have been developed on the Illumina platform for cost-effective genotyping of reference animals of various cattle and buffalo breeds. Understand how the cattle are being selected based on Genomically Estimated Breeding Values (GEBV) calculated using ssGBLUP method for milk yield.
Morphology-driven High-plex Spatial Analysis of Tissue Microenvironments
PastWebinar
Jun 10
Morphology-driven High-plex Spatial Analysis of Tissue Microenvironments
Jun 10, 2020
종양 미세 환경 (TME)에서 면역 구조의 공간적인 특성은(Spatial characterization) 면역 세포와 종양 세포의 연관 관계를 이해하는데 필수적인 요소입니다. 그러나, 제한된 샘플을 사용하여 high multiplexed 실험을 수행하는 것은 매우 어려운 것으로 알려져 있습니다. 이러한 부분을 해결하기 위해 나노스트링사는 단일 FFPE 조직 섹션의 개별적인 위치에서 최대 수백 개의 종양 및 면역 단백질을 동시에 분석하도록 설계된 Imaging/Tissue sampling 플랫폼을 개발하였으며 최근에는 high multiplexed 분석이 가능하도록 동일한 FFPE 조직에서 수천개의 전사체를 프로파일링 할 수 있는 NGS 기반의 RNA 검출 기법이 업데이트 되었습니다. 저희는 DSP (Digital Spatial Profiling)라는 이 새로운 기술을 사용하여, 분석하고자 하는 region의 종양 미세 환경에서 면역 상태에 대한 체계적인 정보를 얻을 수 있는 다양한 단백질과 RNA의 분석을 수행할 수 있습니다. * This webinar is conducted in Korean language and hosted by Illumina in collaboration with NanoString Technologies.
Cell-free DNA screening beyond the common trisomies: A fireside discussion about implementation and clinical implications around the world
PastWebinar
Jun 11
Cell-free DNA screening beyond the common trisomies: A fireside discussion about implementation and clinical implications around the world
Jun 11, 2020
Expanding cell-free DNA screening to more women and a broader range of conditions has transformed the prenatal screening environment, raising questions about who should be offered screening, for what, by whom, and how.
Powering Clinical Metagenomics Analysis to Address  SARS-CoV-2 Detection
PastWebinar
Jun 11
Powering Clinical Metagenomics Analysis to Address SARS-CoV-2 Detection
Jun 11, 2020
Join us for an informative 30-minute webinar with live Q&A that describes the new IDbyDNA SARS-CoV-2 diagnostic workflow solution and how clinical metagenomics can enhance your research use and/or laboratory-developed test offering.
Harnessing the Tumor Immune Microenvironment
PastWebinar
Jun 11
Harnessing the Tumor Immune Microenvironment
Jun 11, 2020
In this webinar, cancer research and immuno-oncology leaders explore new approaches for assessing the potential of transforming and harnessing the tumor immune microenvironment for therapeutic benefit.
Testing approaches for RET alterations in non-small cell lung cancer
PastWebinar
Jun 17
Testing approaches for RET alterations in non-small cell lung cancer
Jun 17, 2020
Dr. Jaclyn Hechtman discusses the relevance of RET alterations in NSCLC and the pros and cons of different technical approaches to test for RET fusions and single-nucleotide variants (SNVs).
DRAGEN BioIT Platform for SARS-CoV-2 and Meta-analysis of Microbiome
PastWebinar
Jun 17
DRAGEN BioIT Platform for SARS-CoV-2 and Meta-analysis of Microbiome
Jun 17, 2020
Join us for a deep dive into how illumina’s DRAGEN BioIT platform supports researchers studying SARS-CoV-2 and metagenomics analysis in general. This analysis pipeline is currently free of use by Oct 2020 as a part of Illumina’s COIVD19 support initiative. In this webinar we will provide an overview on Illumina’s products designed to address COVID19 sequencing requirements, including metagenomics shotgun sequencing, enrichment and amplicon panels. Then we will delve into the details on the SARS-CoV-2 NGS Data Toolkit, including DRAGEN and how this toolkit supports Covid-19 detection, screening and surveillance. We will showcase use of DRAGEN for metagenomics analysis pipeline as a microbiology research tool before finally sharing the latest COVID-Seq announcement from Illumina.
Getting Started with NGS for Oncology Testing
PastWebinar
Jun 18
Getting Started with NGS for Oncology Testing
Jun 18, 2020
Next-generation sequencing (NGS) is changing the future of oncology and advancing the promise of personalized medicine. As genomics-focused pharmacology begins to play a greater role in cancer treatment, NGS is emerging as a valuable method for obtaining a deeper and more accurate look into the molecular underpinnings of individual tumors. With targeted therapies becoming the new standard of care in oncology, NGS-driven companion diagnostics are widely seen as driving the selection of treatments to optimize patient outcomes in the future. At Illumina, our oncology portfolio is helping to drive the revolution in cancer genomics. Our sample-to-data solutions deliver high-quality, reproducible results to speed the discovery and analysis of cancer-related variants, and potentially transform the cancer care cycle. We invite you to this webinar to learn more about implementing oncology NGS workflows in your laboratory, from best practices at the bench to options for clinical reporting. This webinar is hosted by Illumina in collaboration with Premas Life Sciences.
TruSight Oncology 500 ctDNA – Enabling Quality Comprehensive Genomic Profiling from Liquid Biopsy Samples
PastWebinar
Jun 18
TruSight Oncology 500 ctDNA – Enabling Quality Comprehensive Genomic Profiling from Liquid Biopsy Samples
Jun 18, 2020
TruSight Oncology 500 ctDNA is developed to provide comprehensive genomic profiling by analyzing circulating tumor DNA in blood plasma. Detecting essential somatic variants for precision medicine with ctDNA analysis could provide highly valuable information that could eventually benefit patients and facilitate impactful clinical research & trials. This webinar will provide basic introduction of TruSight Oncology 500 ctDNA and will discuss essential features of this solution for oncology testing and potential clinical research. *This webinar will be conducted in Korean
Illumina’s Targeted Approaches to Cancer Variant Detection
PastWebinar
Jun 22
Illumina’s Targeted Approaches to Cancer Variant Detection
Jun 22, 2020
This webinar aims to give an overview of Illumina’s targeted approaches to detection of cancer variants, covering both amplicon and targeted enrichment panels. There are a wide variety of options available depending on the scope and scale of the project being undertaken. Following a discussion of the range of different panels that Illumina provides, as well as how to go about designing custom panels, this webinar will highlight some of the tools we have available to help with selection of the best panel for your needs. There will be a Q & A session at the end.
Building Global Startups
PastWebinar
Jun 23
Building Global Startups
Jun 23, 2020
Join the Illumina and four global genomics startups in the biotech, clinical, and agricultural industries to discuss key trends in entrepreneurship.
NextSeq™ 2000: One instrument, a range of applications
PastWebinar
Jun 23
NextSeq™ 2000: One instrument, a range of applications
Jun 23, 2020
See a virtual instrument demo of the NextSeq 2000 and learn more about these solutions enabled by Illumina’s newest platform followed by open audience Q&AS
Building Global Startups
PastWebinar
Jun 23
Building Global Startups
Jun 23, 2020
Join the Illumina and four global genomics startups in the biotech, clinical, and agricultural industries to discuss key trends in entrepreneurship.
Employing Clinical Metagenomics for Improved Uropathogen Detection
PastWebinar
Jun 24
Employing Clinical Metagenomics for Improved Uropathogen Detection
Jun 24, 2020
Understand the workflow solution using Illumina's UTI solution with IDbyDNA's Explify for clinical applications.
Metabarcoding in Marine Eukaryotes
PastWebinar
Jun 24
Metabarcoding in Marine Eukaryotes
Jun 24, 2020
Next-generation sequencing (NGS) technologies have made it possible to obtain millions of sequence reads in a single experiment, and massively parallel sequencing (MPS) is currently revolutionizing survey of environmental DNA (eDNA), because this technology enables us to detect several hundreds of operational taxonomic units (OTUs) of bacteria and eukaryotes from aquatic environmental samples and facilitates the detection of low-abundance populations from complex communities. In this seminar, Dr. Nagai would be introducing the interesting results of eukaryote metabarcoding carried out mainly in Japanese coastal waters.
Prioritizing functional genetic variants through advance sequencing approaches
PastWebinar
Jun 30
Prioritizing functional genetic variants through advance sequencing approaches
Jun 30, 2020
See how recent advances in sequencing technologies have allowed for the development of genomics-based strategies for assaying GWAS SNPs for potential functional relevance.
Spatial analysis of the tumor and its microenvironment with Illumina Sequencing and NanoString Technologies
PastWebinar
Jul 07
Spatial analysis of the tumor and its microenvironment with Illumina Sequencing and NanoString Technologies
Jul 7, 2020
Discover the latest news on how Illumina and Nanostring help to deliver on the promise of spatial biology.
Cluster Optimization Overview [Korean]
PastWebinar
Jul 08
Cluster Optimization Overview [Korean]
Jul 8, 2020
This webinar will cover critical parameters for optimizing cluster density on both our patterned and non-patterned flow cells. We will cover the following topics: factors that impact cluster efficiency; review of the clusters passing filter metric; how to diagnose clustering issues; and tips and tricks to achieve optimal density across our varying sequencing platforms. * Please note that this webinar will be conducted in Korean language. If you are not able to make it in this time, please feel free to register to be notified when it is available on-demand where you can watch it at your convenience.
Validating Short Tandem Repeats by Genome Sequencing in the Illumina Clinical Services Lab
PastWebinar
Jul 08
Validating Short Tandem Repeats by Genome Sequencing in the Illumina Clinical Services Lab
Jul 8, 2020
Patients and their families can spend many years hoping to reach a diagnosis for their rare disease. Whole genome sequencing (WGS) enables the most extensive analysis of the genome, including analysis of coding and noncoding regions, comprehensive variant class detection, and findings that can be coupled with epigenetic or transcriptomic evaluations. Listen as Dr. Tanner Hagelstrom discusses the clinical validation of short tandem repeats (STRs), introducing this unique variant class to a whole genome sequencing workflow.
Our Magic DRAGEN: A Sequencing Lab Case Study on Accelerated Bioinformatics
PastWebinar
Jul 09
Our Magic DRAGEN: A Sequencing Lab Case Study on Accelerated Bioinformatics
Jul 9, 2020
Dr. Charlie Johnson, Texas A&M, on utilizing Illumina’s DRAGEN informatics platform in its high-throughput agrigenomics research program.
Illumina DRAGEN Bio-IT Platform: What’s new with version 3.6
PastWebinar
Jul 10
Illumina DRAGEN Bio-IT Platform: What’s new with version 3.6
Jul 10, 2020
The DRAGEN team is excited to announce the release of DRAGEN version 3.6. This version includes significant runtime improvements to the germline and somatic variant calling pipelines with the implementation of deBrujin graph construction on the DRAGEN FPGA. We are also excited to announce support for FASTQC statistics generation, poly-G trimming, and improvements to the JointGenotyping and CNV pipelines. This webinar is intended for all customers interested in hearing more about what’s new in DRAGEN. These features will be made available for on-site customers and also Cloud users on various platforms like BaseSpace and AWS Marketplace.
Liquid Biopsy: An Attractive Proposition and its Scope
PastWebinar
Jul 14
Liquid Biopsy: An Attractive Proposition and its Scope
Jul 14, 2020
Liquid biopsy is an alternative to tissue biopsy and can play a major role in cancer targeted therapy, predominantly in NSCLC. New biopsy is required in NSCLC progressed patients to determine resistance mechanism. Re-biopsy is a challenge. Tissue vs liquid biopsy results are highly concordant however, 30% false negative result reported. Clinical utility of liquid biopsy (ctDNA) has been established in several clinical trials. Monitoring of molecular resistance in tumor is possible through liquid biopsy (ctDNA). Dynamic changes in disease molecular profile can be determined by liquid biopsy. Highly sensitive and validated method should be employed to correctly genotype the tumor. Thus liquid biopsy tests may offer an easier way to spot cancer's footprints.
Comprehensive Genomic Profiling liquid biopsy trends in clinical trials
PastWebinar
Jul 14
Comprehensive Genomic Profiling liquid biopsy trends in clinical trials
Jul 14, 2020
Discussion of workflow and bioinformatics considerations when consolidating independent biomarkers into a panel that enables CGP from liquid biopsy samples in translational research.
Environmental DNA for Eco-Evo Monitoring of Aquatic Organisms in the New Era
PastWebinar
Jul 15
Environmental DNA for Eco-Evo Monitoring of Aquatic Organisms in the New Era
Jul 15, 2020
Environmental DNA (eDNA) is increasingly recognized as an efficient tool for detecting organisms in the wild. The eDNA technology utilizes DNA from environmental samples, such as river/sea water, as evidence of the presence of wild organisms nearby. This webinar will discuss how to collect and analyze eDNA, as well as its real-world applications to Eco-Evo monitoring of fish species with Next-Generation Sequencing technology.
Environmental DNA (eDNA) and Metabarcoding
PastWebinar
Jul 15
Environmental DNA (eDNA) and Metabarcoding
Jul 15, 2020
This webinar reviews recent research and validation experiments demonstrating the power of metabarcoding for a range of potential applications.
Next-Generation Sequencing (NGS) based Approach for Food Safety Pathogen Analysis [Korean]
PastWebinar
Jul 21
Next-Generation Sequencing (NGS) based Approach for Food Safety Pathogen Analysis [Korean]
Jul 21, 2020
In this webinar, Kenny will talk about NGS application for food safety. Through this webinar he will explain the differences between traditional method and NGS applications and why we should adopt NGS platform for food safety. Especially WGS can identify the bacterial genomes of pathogens, increasing the accuracy of microbial testing so it can be used as a valuable tool in investigating outbreaks and tracing the cause back to the source. * This webinar will be conducted in Korean.
Investigating functional microglial diversity in Alzheimer’s disease using RNA Sequencing
PastWebinar
Jul 24
Investigating functional microglial diversity in Alzheimer’s disease using RNA Sequencing
Jul 24, 2020
The important role of microglia in Alzheimer’s disease (AD) is well recognized, however their molecular and functional diversity and underlying mechanisms still remain controversial. To transcriptionally and functionally characterize the diversity of microglia in AD and aging, we isolated the amyloid plaque-containing (XO4+) and non-containing (XO4-) microglia from an AD mouse model. Transcriptomics analysis unveiled independent transcriptional trajectories in ageing and AD. XO4+ microglial transcriptomes linked plaque phagocytosis to dysregulated expression of bona fide late onset AD genetic risk factors. To determine whether the XO4+ signature occurs in human AD, we applied single-nucleus RNA sequencing to entorhinal cortex samples from control and AD brains (n = 6 per group). We revealed that features of the XO4+ transcriptional program are present in a subset of human microglia from AD patients. Conversely, XO4- microglia in AD displayed an accelerated ageing signature and contained more intracellular post synaptic material than plaque-containing microglia, despite reduced active synaptosome phagocytosis. We identified Hif1α as a regulator of the XO4-/XO4+ axis, and validated the functional role of Hif1α on synaptosome phagocytosis in vitro. Together these findings unveiled the molecular mechanism underpinning the functional diversity of microglia in AD. Finally, our single nuclei resource describes cell-type-specific gene expression patterns in AD, and allowed us to discover how genetic predisposition to AD manifests in specific brain cell subpopulations and to predict the master switches involved. These results provide insights into the coordinated control of AD risk genes and their cell-type-specific contribution to disease susceptibility.
Library Quantification and QC Methods
PastWebinar
Jul 30
Library Quantification and QC Methods
Jul 30, 2020
When designing a next generation sequencing project, both library concentration and library quality are critical parameters to measure and control. This webinar will review the common methods of library quantification and QC and discuss pros and cons for each method. We will highlight recommended methods for libraries prepared with all current Illumina kits and then review examples of optimal and suboptimal library QC results. We will wrap up by reviewing troubleshooting methods that can be employed when sub-optimal libraries (or simply library traces) are detected.
Cancer genomics and single-cell technologies
PastWebinar
Jul 31
Cancer genomics and single-cell technologies
Jul 31, 2020
In this Nature Research webcast, three experts discuss cancer genomics and single-cell technologies, the unique analytical considerations and potential to yield biological discoveries.
From Variant to Function: Using Multi-Omics to understand blood disorders
PastWebinar
Aug 05
From Variant to Function: Using Multi-Omics to understand blood disorders
Aug 5, 2020
Multi-omics sequencing is a powerful approach for evaluating variant effects through measurement of multiple layers of information.
Using Stem Cells to Explore the Genetics Underlying Neuropsychiatric Disease
PastWebinar
Aug 05
Using Stem Cells to Explore the Genetics Underlying Neuropsychiatric Disease
Aug 5, 2020
Integrating whole-genome or whole-exome sequencing data with transcriptome information (from RNAseq) and epigenetic information (from methylation arrays) in tissue types of interest can help identify genes and pathways that have a role in particular diseases.
Using Stem Cells to Explore the Genetics Underlying Neuropsychiatric Disease
PastWebinar
Aug 05
Using Stem Cells to Explore the Genetics Underlying Neuropsychiatric Disease
Aug 5, 2020
Integrating whole-genome or whole-exome sequencing data with transcriptome information (from RNAseq) and epigenetic information (from methylation arrays) in tissue types of interest can help identify genes and pathways that have a role in particular diseases.
Gene-Level Metagenomics for Microbiome Research
PastWebinar
Aug 12
Gene-Level Metagenomics for Microbiome Research
Aug 12, 2020
Learn about a novel gene-level bioinformatics approach for identifying microbial species and strains associated with human disease from metagenomic sequencing datasets.
Precision Medicine in Action: Zero Childhood Cancer - Australia’s Comprehensive Precision Medicine Program for Kids with Cancer
PastWebinar
Aug 18
Precision Medicine in Action: Zero Childhood Cancer - Australia’s Comprehensive Precision Medicine Program for Kids with Cancer
Aug 18, 2020
The Zero Childhood Cancer Program (ZERO) is a game-changer in the care of child cancers in Australia. It is blazing a trail to embed precision medicine in mainstream healthcare, improving health outcomes for children and adults alike. The aim throughout ZERO has been to lay the foundations of a path to implementing a personalised medicine program within the Australian health system. In this webinar, Ness will talk about precision medicine in action through the Zero Childhood Cancer Program and her goal to see that all children with cancer will have equitable access to precision medicine and lead the adoption of this model of care across multiple clinical disciplines.
DNA Methylation Profiling to Predict Risk Recurrence in Meningioma
PastWebinar
Aug 19
DNA Methylation Profiling to Predict Risk Recurrence in Meningioma
Aug 19, 2020
Dr. Gelareh Zadeh and Dr. Farshad Nassiri highlight transformative work using DNA Methylation technology and methylome-based predictors.
A Single Cell Atlas of Human Liver: Implications in Pathobiology
PastWebinar
Aug 20
A Single Cell Atlas of Human Liver: Implications in Pathobiology
Aug 20, 2020
Liver dysfunction is associated with diseases ranging from metabolic disorders to hepatocellular carcinomas (HCC). We employed single-cell RNA-sequencing to extensively characterize the cellular landscape (~212,000 cells) of the human liver, from development to disease. In this webinar, Ankur will share the insights from scRNA-seq into the heterogeneity of TME and the dynamics of cell-cell interactions in the healthy and diseased ecosystem. Currently, we are living through an unprecedented global pandemic COVID-19. In this webinar, Ankur will share the implication of scRNA-seq atlas in identifying cell types potentially susceptible to SARS-CoV-2 infection.
Comprehensive genomic profiling from liquid biopsy samples in clinical trials
PastWebinar
Aug 20
Comprehensive genomic profiling from liquid biopsy samples in clinical trials
Aug 20, 2020
We will discuss critical workflow and bioinformatics considerations when consolidating biomarkers testing into a panel that enables CGP from liquid biopsy.
Precision Oncology Asia: Challenges in Paediatric Glioblastoma
PastWebinar
Aug 22
Precision Oncology Asia: Challenges in Paediatric Glioblastoma
Aug 22, 2020
The advancement in technologies like Genomics and Data Science has paved the way for precision oncology, which allows tailored medical treatment based on individual characteristic of each patient and their tumour. Precision oncology Asia is a platform to bring together clinicians, academicians, industries and startups onto a common platform to share their experiences on how they utilize these technologies to come out with solutions to improve patient outcomes.
Implementing Comprehensive Genomic Profiling (CGP) to Streamline Identification of Actionable Biomarkers
PastWebinar
Aug 23
Implementing Comprehensive Genomic Profiling (CGP) to Streamline Identification of Actionable Biomarkers
Aug 23, 2020
With hundreds of biomarkers linked to approved drugs and ongoing clinical trials comes a need for consolidated testing in a single assay. Comprehensive Genomic Profiling (CGP) is a powerful assay that enables simultaneous detection of 500+ oncology biomarkers in single, next-generation sequencing test; identifies actionable biomarkers that help optimize treatment. In a series of studies, up to 90% of patients had actionable alterations as a result of CGP testing; and provides faster results using fewer samples for increased efficiency. Watch this webinar with Dr. Gerald Goh to learn how CGP is improving biomarker detection, leading to actionable insights and increased efficiencies.
GenomeStudio Genotyping: Creating Custom Cluster Files for Infinium Arrays
PastWebinar
Aug 28
GenomeStudio Genotyping: Creating Custom Cluster Files for Infinium Arrays
Aug 28, 2020
Join this webinar to learn how to create custom cluster files for Infinium Arrays. This webinar includes the following topics: Cluster file basics, when to use a custom cluster file, how to create a custom cluster file, and how to filter and manually edit to optimize the cluster file. The information is targeted to new and intermediate users with a basic knowledge of working with Genotyping Data in GenomeStudio.
From Bedside to Bench: Immune profiling of human tumors identifies CD73 as a combinatorial target in glioblastoma.
PastWebinar
Sep 01
From Bedside to Bench: Immune profiling of human tumors identifies CD73 as a combinatorial target in glioblastoma.
Sep 1, 2020
This talk will highlight the use of single cell RNA-sequencing to identify a unique population of macrophages in glioblastoma multiforme that persists after treatment with immune checkpoint inhibitors.
Optimise. Validate. Discover – Paving the way to a successful Single-cell Multi-omics Analysis
PastWebinar
Sep 02
Optimise. Validate. Discover – Paving the way to a successful Single-cell Multi-omics Analysis
Sep 2, 2020
In this webinar we will provide an overview of the Dolomite Bio and Illumina platforms, as well as the workflow, which when coupled together, provides an end-to-end solution for varying cell types, sizes and applications. We are also pleased to be joined by guest speaker Aki Minoda from RIKEN, who will discuss her research using the platforms and how it is has been key in optimising and developing experiments within projects such as mouse ageing and plant studies. Join us to see how customisable single-cell workflows are within your reach and gain insight into the ongoing research at the Laboratory for Cellular and Epigenomics using single cell platforms.
The Regulatory Landscape of Arabidopsis Thaliana Roots at Single-Cell Resolution
PastWebinar
Sep 08
The Regulatory Landscape of Arabidopsis Thaliana Roots at Single-Cell Resolution
Sep 8, 2020
In plants, chromatin accessibility – the primary mark of regulatory DNA – is relatively static across tissues and conditions.
Morphology-driven high-plex spatial analysis of tissue microenvironments
PastWebinar
Sep 14
Morphology-driven high-plex spatial analysis of tissue microenvironments
Sep 14, 2020
Spatial characterization of the immune contexture in the tumor microenvironment (TME) is essential for understanding the relationship between immune and tumor cells. However, it has proven difficult to perform such studies in a highly multiplexed manner using limited samples. To address this unmet need, we have developed an imaging and tissue-sampling platform designed to simultaneously analyze up to hundreds of tumor and immune proteins in distinct locations on a single FFPE tissue section. To supplement this capacity, we have recently developed an RNA detection chemistry that can profile thousands of transcripts using NGS sequencing platforms on the same FFPE sample types. Using this novel technology, called Digital Spatial Profiling (DSP), we demonstrate multiplexed protein and RNA analysis of defined regions of interest within a tumor enabling systematic interrogation of the immune status in the tumor microenvironment.
Sample Prep and Quality Control for Single Cell Sequencing Experiments
PastWebinar
Sep 14
Sample Prep and Quality Control for Single Cell Sequencing Experiments
Sep 14, 2020
Quality single cell sequencing results depend on good libraries and good libraries start with sample prep. Learn how to optimize the upstream workflow to ensure successful single cell sequencing experiments.
Use of Combinatorial Single Cell Technologies to Drive Deeper Immune Discoveries
PastWebinar
Sep 14
Use of Combinatorial Single Cell Technologies to Drive Deeper Immune Discoveries
Sep 14, 2020
We will highlight several applications of fully supported workflows with Becton Dickinson and Illumina that can take you from single cell suspensions to final analyzed data and confirmatory experiments to better understand the human immune system and its role in important biological functions.
Enabling High Resolution Spatial Profiling with Next Generation Sequencing
PastWebinar
Sep 14
Enabling High Resolution Spatial Profiling with Next Generation Sequencing
Sep 14, 2020
To date, most gene expression studies have been performed using various methods ranging from relative quantitative PCR, microarray, and Next Generation Sequencing (NGS) on bulk samples consisting many cells from a sample. Only recently we have seen an explosion of NGS data created from the transcriptome of single cells that make up a sample to reveal heterogeneity in cells of the same sample. Now with spatial transcriptomics we can discover gene expression profiles of specified regions of tissue samples on common histology slides giving insight into micro-environmental differences. NGS enables this high resolution, high throughput methodology through a range of gold standard sequencing instruments and well known sequencing chemistries to provide high quality data for downstream analyses. Today we will provide some guidance on experimental planning, instrument choice and information on the latest sequencing technology for your spatial transcriptomics work.
Comprehensive Genomic Profiling: A new paradigm in oncology
PastWebinar
Sep 22
Comprehensive Genomic Profiling: A new paradigm in oncology
Sep 22, 2020
Hear from expert oncologists and pathologists how NGS-based comprehensive genomic profiling assays are changing the paradigm in oncology. On Demand recordings of ESMO Industry Satellite Symposium.
Comprehensive Genomic Profiling: A new paradigm in oncology
PastWebinar
Sep 22
Comprehensive Genomic Profiling: A new paradigm in oncology
Sep 22, 2020
Hear from expert oncologists and pathologists how NGS-based comprehensive genomic profiling assays are changing the paradigm in oncology. On Demand recordings of ESMO Industry Satellite Symposium.
Getting Started With Single Cells: Targeted Gene Expression
PastWebinar
Sep 23
Getting Started With Single Cells: Targeted Gene Expression
Sep 23, 2020
You will learn how to combine crucial insights enabled by single cell gene expression analysis with the efficiency and scalability of pre-designed or custom panels. We will also review important considerations for Next Generation Sequencing experimental planning. This webinar will consist of two 15-20 minute presentations followed by a live Q&A session.
Detect multiple respiratory viruses including SARS-COV-2
PastWebinar
Sep 23
Detect multiple respiratory viruses including SARS-COV-2
Sep 23, 2020
Viral infections are a major global health concern, with new infectious diseases continuing to emerge. Next-generation sequencing (NGS) is a powerful method for the broad-range detection and identification of known and emerging respiratory viruses, including SARS-CoV-2. In this webinar, Jon Hetzel will introduce our new respiratory virus oligo panel (RVOPv2) and workflow that combines a new RNA library prep and viral target enrichment. In this webinar, Jon will introduce our new respiratory virus panel (RVOPv2) combined with the new RNA library prep with enrichment kit. RVOPv2 offers an easy-to-follow workflow, improved sensitivity for both detection and full genome characterization of multiple respiratory pathogens in one test. Target enrichment for a broad range of respiratory viruses enables the detection and monitoring of co-infections which can present a major challenge in disease treatment.
BaseSpace Variant Interpreter: An Introduction
PastWebinar
Sep 29
BaseSpace Variant Interpreter: An Introduction
Sep 29, 2020
This webinar will cover critical parameters for optimizing cluster density on both our patterned and non-patterned flow cells. We will cover the following topics: factors that impact cluster efficiency; review of the clusters passing filter metric; how to diagnose clustering issues; and tips and tricks to achieve optimal density across our varying sequencing platforms.
DRAGEN-GATK Best Practices: A Deep Dive into Genomic Analysis Pipeline Improvements
PastWebinar
Sep 29
DRAGEN-GATK Best Practices: A Deep Dive into Genomic Analysis Pipeline Improvements
Sep 29, 2020
The Broad Institute and Illumina have partnered to co-develop and improve upon genomic analysis pipelines, starting with integrating methods from Illumina’s DRAGEN (Dynamic Read Analysis for GENomics) hardware-accelerated informatics platform into the Broad Institute’s GATK (Genomic Analysis ToolKit) Best Practices small variant pipeline, resulting in DRAGEN-GATK Best Practices. In this webinar, Eric Banks of the Broad Institute will describe some of the issues the development team encountered as it investigated the differences between DRAGEN and GATK tools, highlighting the improvements to methods implemented in the new Best Practices pipeline. He will also explain how the team assessed functional equivalency between the open source and licensed (hardware-accelerated) version of the pipeline, showing results between the two methods on the same source input.
Increasing Equity in 
Genomic Healthcare
PastWebinar
Sep 29
Increasing Equity in 
Genomic Healthcare
Sep 29, 2020
Join a panel of thought leaders as they discuss ways our community can work towards more equitable genomic healthcare. #genomicsequity
DRAGEN-GATK Best Practices: A Deep Dive into Genomic Analysis Pipeline Improvements
PastWebinar
Sep 29
DRAGEN-GATK Best Practices: A Deep Dive into Genomic Analysis Pipeline Improvements
Sep 29, 2020
In this webinar, Eric Banks of the Broad Institute will describe some of the issues the development team encountered as it investigated the differences between DRAGEN and GATK tools
Single Cell Approaches to Lineage Tracing in Stem and Developmental Biology
PastWebinar
Sep 30
Single Cell Approaches to Lineage Tracing in Stem and Developmental Biology
Sep 30, 2020
Join us for a discussion of lineage tracing of stem cell and developmental dynamics using single cell technologies and imaging based screens
The Genomic Insights in Rare Disease Webinar Series
PastWebinar
Oct 01
The Genomic Insights in Rare Disease Webinar Series
Oct 1, 2020
Listen as top experts in the field share how their work is impacting the ability to find an answer in rare disease.
Spatial landscape of the immune microenvironment in metastatic prostate cancer using GeoMx™ Digital Spatial Profiler
PastWebinar
Oct 05
Spatial landscape of the immune microenvironment in metastatic prostate cancer using GeoMx™ Digital Spatial Profiler
Oct 5, 2020
A spatial genomics approach to defining the microenvironment landscape of molecular subtypes of mPC, potentially revealing patterns in the metastatic microenvironments that may predict the utility of immune-based therapies.
Whole-Genome Sequencing Comes of Age in Clinical Care
PastWebinar
Oct 08
Whole-Genome Sequencing Comes of Age in Clinical Care
Oct 8, 2020
Listen to Dr. Liz Worthey, Director Ctr Genomic Data Sciences Dept Pediatrics/Pathology, UAB speak to the implementation of “Omics-based Precision Medicine methods in 2020”
Future Applications and Impact Potential of Targeted Enrichment for Disease and AMR Detection
PastWebinar
Oct 22
Future Applications and Impact Potential of Targeted Enrichment for Disease and AMR Detection
Oct 22, 2020
Clinical metagenomics has paved the way for un-biased, culture-free detection and identification of a broad number of pathogens and genetic markers of antimicrobial resistance.
The Genetics of Cardiovascular Disease - from Leonardo to Precision Diagnostics
PastWebinar
Oct 27
The Genetics of Cardiovascular Disease - from Leonardo to Precision Diagnostics
Oct 27, 2020
Expert who is using Illumina technology offered updates at ASHG 2020
Getting Started With Spatial Technology: Targeted Gene Expression
PastWebinar
Oct 27
Getting Started With Spatial Technology: Targeted Gene Expression
Oct 27, 2020
You will learn how to combine crucial insights enabled by spatial gene expression analysis with the efficiency and scalability of pre-designed or custom panels. We will also review important considerations for Next Generation Sequencing experimental planning. This webinar will consist of two 15-20 minute presentations followed by a live Q&A session.
COVID19-HGI: A global effort to identify host genetics contributions to susceptibility and severity
PastWebinar
Oct 27
COVID19-HGI: A global effort to identify host genetics contributions to susceptibility and severity
Oct 27, 2020
Expert who is using Illumina technology offered updates at ASHG 2020
Sequencing Low Diversity Libraries
PastWebinar
Oct 27
Sequencing Low Diversity Libraries
Oct 27, 2020
This support webinar is ideal for new and intermediate users interested in considerations for the sequencing of low diversity libraries and will cover the following topics: understanding and visualising base diversity in Sequencing Analysis Viewer (SAV), strategies to optimise low diversity sequencing data, % PhiX spike-in and cluster density recommendations for different sequencing platforms, and an overview of base calling and quality score calculations.
Advancing the Future of Genomics, Together
PastWebinar
Oct 27
Advancing the Future of Genomics, Together
Oct 27, 2020
Expert who is using Illumina technology offered updates at ASHG 2020
How to Train Your DRAGEN for Pathology Informatics
PastWebinar
Oct 29
How to Train Your DRAGEN for Pathology Informatics
Oct 29, 2020
In this webinar, Lynn Fink of Xing Cancer Care will discuss how her ISO15189-accredited lab has used Illumina’s BaseSpace Sequence Hub (BSSH) to support informatics data analysis as part its routine testing and will share details of why the lab chose this platform over other options.
How Comprehensive Genomic Profiling is becoming Standard-of-Care in Oncology
PastWebinar
Nov 04
How Comprehensive Genomic Profiling is becoming Standard-of-Care in Oncology
Nov 4, 2020
Is CGP is becoming standard-of-care in oncology? In this webinar, Assoc. Prof. Nick Pavlakis from the Clinical Oncology Society of Australia will share his experience with the ASPiRATION trial for Lung Cancer & Dr. Mithua Ghosh from HCG Oncology will speak about personalized cancer treatment
Next-generation sequencing (NGS) applications for SARS-CoV-2 detection and surveillance
PastWebinar
Nov 10
Next-generation sequencing (NGS) applications for SARS-CoV-2 detection and surveillance
Nov 10, 2020
Discussion of the applicability of NGS for responding to the SARS-CoV-2 pandemic, from initial detection.
Challenges in Clinical Metagenomics: Identifying Pathogenic Organisms in the Background of a Variable Microbiome
PastWebinar
Nov 11
Challenges in Clinical Metagenomics: Identifying Pathogenic Organisms in the Background of a Variable Microbiome
Nov 11, 2020
Clinical metagenomics using next-generation sequencing has the potential to create a seismic shift in the care of patients who suffer from infections.
Leveraging genomics to accelerate genetic improvement in aquaculture
PastWebinar
Nov 11
Leveraging genomics to accelerate genetic improvement in aquaculture
Nov 11, 2020
Current achievements on the application of genomic technologies for selective breeding aquaculture species
Leveraging genomics to accelerate genetic improvement in aquaculture
PastWebinar
Nov 11
Leveraging genomics to accelerate genetic improvement in aquaculture
Nov 11, 2020
Current achievements on the application of genomic technologies for selective breeding aquaculture species
Challenges in Clinical Metagenomics: Identifying Pathogenic Organisms in the Background of a Variable Microbiome
PastWebinar
Nov 11
Challenges in Clinical Metagenomics: Identifying Pathogenic Organisms in the Background of a Variable Microbiome
Nov 11, 2020
Clinical metagenomics using next-generation sequencing has the potential to create a seismic shift in the care of patients who suffer from infections.
How To Plan Your First Sequencing Project
PastWebinar
Nov 12
How To Plan Your First Sequencing Project
Nov 12, 2020
This webinar aims to give an overview of how to get started with planning your first sequencing project. It includes a discussion of upfront considerations, as well as options for library prep, sequencing and analysis. We will talk about many of the useful resources that are available for new and more experienced users when starting a new project. We will end with a Q&A session.
What’s new in DRAGEN v3.7: Single Cell RNA, PrecisionFDA accuracy gains, and more
PastWebinar
Nov 17
What’s new in DRAGEN v3.7: Single Cell RNA, PrecisionFDA accuracy gains, and more
Nov 17, 2020
Shyamal Mehtalia, Principal Engineer, Illumina Inc.
확장된 비침습적 산전검사(Expanded NIPT): 임상 사례 및 임상적 유용성
PastWebinar
Nov 24
확장된 비침습적 산전검사(Expanded NIPT): 임상 사례 및 임상적 유용성
Nov 24, 2020
일루미나의 비침습적 산전검사(NIPT)는 확장된(expanded) 검사를 가능하게 하는 전장유전체서열분석(WGS)을 기반으로 합니다. 확장된 비침습적 산전검사(expanded NIPT)는 흔한 염색체 이수성(21번, 18번, 13번, 성염색체) 뿐만 아니라 희귀 상염색체 이수성(Rare Autosomal Aneuploidy, RAA)과 모든 상염색체 상에서 7Mb 이상의 유전자 복제수변이(Copy Number Variation, CNV)를 의미하는 부분 결실 및 중복(partial deletion and duplication)을 검출합니다.
Personalized Medicine Based on Common & Rare Genetic Variants in Estonia
PastWebinar
Dec 01
Personalized Medicine Based on Common & Rare Genetic Variants in Estonia
Dec 1, 2020
Dr. Lili Milani talks about the personalized medicine initiative that she’s been leading at the Estonian Biobank.
Implementing Genomics in Healthcare – An Estonian Perspective
PastWebinar
Dec 01
Implementing Genomics in Healthcare – An Estonian Perspective
Dec 1, 2020
Dr. Tonu Esko walks through the Estonian Biobank initiative and its efforts to implement pharmacogenomics at the national healthcare level.
Implementing Genomics in Healthcare – An Estonian Perspective
PastWebinar
Dec 01
Implementing Genomics in Healthcare – An Estonian Perspective
Dec 1, 2020
Dr. Tonu Esko walks through the Estonian Biobank initiative and its efforts to implement pharmacogenomics at the national healthcare level.
Virtual Oncology/SARS-CoV-2 Impact Fireside Chat
PastWebinar
Dec 02
Virtual Oncology/SARS-CoV-2 Impact Fireside Chat
Dec 2, 2020
Oncology patients are heavily impacted by the ongoing SARS-CoV-2 pandemic.
Assaying genome-wide chromatin accessibility with ATAC-seq
PastWebinar
Dec 17
Assaying genome-wide chromatin accessibility with ATAC-seq
Dec 17, 2020
This webcast will show participants how to use ATAC-seq and how it fits in with other chromatin accessibility profiling methods.
Next-Generation Sequencing & High-Throughput Genotyping for Climate Resilient & Higher Nutrition Crop Varieties in Legumes
PastWebinar
Jan 13
Next-Generation Sequencing & High-Throughput Genotyping for Climate Resilient & Higher Nutrition Crop Varieties in Legumes
Jan 13, 2021
In this webinar, Professor Rajeev Varshney will be presenting on next-generation sequencing (NGS) and high-throughput genotyping (HTPG) technologies coupled with advances in computational biology that has started a new era of genomic breeding for crop improvement.
Turbocharging Fruit Tree Breeding [Recording from ICQG6 2020]
PastWebinar
Jan 13
Turbocharging Fruit Tree Breeding [Recording from ICQG6 2020]
Jan 13, 2021
The allelic diversity of primitive germplasm of fruit crops provides a useful resource for introgressing novel genes to meet consumer preferences and environmental challenges. Pre-breeding facilitates the identification of novel genetic variation in the primitive germplasm and expedite its utilisation in cultivar breeding programmes. Several generations of pre-breeding could be required to minimise linkage drag from the donor parent and to maximise the genomic content of the recipient parent. In this study we investigated the potential of genomic selection (GS) as a tool for rapid background selection of parents for the successive generation. In this webinar, Dr Kumar will discuss the overview of breeding designs, the genetic architecture of economically important traits and genomic selection for fruit tree breeding.
Infinium Mouse Methylation BeadChip
PastWebinar
Jan 19
Infinium Mouse Methylation BeadChip
Jan 19, 2021
The first Illumina methylation array for model organisms, the Infinium™ Mouse Methylation BeadChip offers comprehensive, expert-selected coverage of 285,000 CpG sites across the mouse methylome with high throughput capacity at an affordable price. In this webinar, we’ll provide the information including product overview, workflow, basic data and ordering information including time-limited promotion.
Overview of llumina’s newest instruments, the NextSeq 1000/2000
PastWebinar
Jan 29
Overview of llumina’s newest instruments, the NextSeq 1000/2000
Jan 29, 2021
Attend this webinar to learn about Illumina’s newest instruments: the NextSeq 1000 and NextSeq 2000. The NextSeq 1000/2000 Sequencing Systems are the latest NGS system from Illumina and offer innovative design features, advanced chemistry, simplified bioinformatics, and an intuitive workflow that enable the widest range of applications on a benchtop sequencing system. The NextSeq 1000/2000 Sequencing Systems leverage the latest advances in optics, instrument design, and reagent chemistry to miniaturize the volume of the sequencing reaction while increasing output and reducing the cost per run. Now, users can obtain the throughput, data quality, and cost needed to expand the size and scope of their studies, all on a benchtop sequencing system. The NextSeq 1000/2000 Sequencing Systems take advantage of an integrated cartridge that includes reagents, fluidics, and the waste holder, simplifying library loading and instrument use. Simply thaw the reagent cartridge, insert the flow cell into the cartridge, load the library into the cartridge, and insert the assembled cartridge into the instrument.
Transform Broad Respiratory Pathogen Detection with the Power of Precision Metagenomics
PastWebinar
Feb 11
Transform Broad Respiratory Pathogen Detection with the Power of Precision Metagenomics
Feb 11, 2021
With the rapid advances in next-generation sequencing (NGS) technologies, clinical and public health microbiology laboratories are increasingly adopting metagenomics into their existing laboratory workflows for infectious disease detection.
Single Nuclei Profiling Identifies Cell Specific Markers of Skeletal Muscle Aging, Sarcopenia and Senescence
PastWebinar
Feb 17
Single Nuclei Profiling Identifies Cell Specific Markers of Skeletal Muscle Aging, Sarcopenia and Senescence
Feb 17, 2021
Aging is accompanied by a loss of muscle mass and function, termed sarcopenia, which causes numerous morbidities and economic burdens in human populations. Mechanisms implicated in age-related sarcopenia include inflammation, muscle stem cell depletion, mitochondrial dysfunction and loss of motor neurons, but whether there are key drivers of sarcopenia is not yet known. To gain deeper insights into age-related sarcopenia, we performed transcriptome profiling on lower limb muscle biopsies from 72 young, old and sarcopenic subjects using bulk RNA-seq (N = 72) and single-nuclei RNA-seq (N = 17). This combined approach revealed novel changes in gene expression that occur with age and sarcopenia in multiple cell types comprising mature skeletal muscle. To validate our findings, we performed digital spatial profiling to confirm key genes identified in our bulk and single nuclei gene expression studies on fixed human muscle tissue. We also identified a small population of nuclei that express CDKN1A, present only in aged samples, consistent with p21-driven senescence in this subpopulation. Overall, our findings identify unique cellular subpopulations in aged and sarcopenic skeletal muscle, which will facilitate the development of new therapeutic strategies to combat age-related sarcopenia.
Transform Broad Respiratory Pathogen Detection with the Power of Precision Metagenomics
PastWebinar
Feb 25
Transform Broad Respiratory Pathogen Detection with the Power of Precision Metagenomics
Feb 25, 2021
With the rapid advances in next-generation sequencing (NGS) technologies, clinical and public health microbiology laboratories are increasingly adopting metagenomics into their existing laboratory workflows for infectious disease detection.
An introduction to RNA-Seq data analysis
PastWebinar
Feb 26
An introduction to RNA-Seq data analysis
Feb 26, 2021
In this webinar, we will discuss various bioinformatic tools available from Illumina to perform RNA-Seq data analysis. This will include an overview of different types of RNA-Seq Analysis such as Differential Expression Analysis, Novel transcript assembly and how to combine different Apps on BaseSpace to perform these analyses. We will also discuss the similarities and differences in workflow and output generated by these Apps.
Comprehensive Genomic Profiling in Lung Cancer:
PastWebinar
Mar 04
Comprehensive Genomic Profiling in Lung Cancer:
Mar 4, 2021
Lung cancer accounts for more cancer deaths per year than any other cancer and the majority of patients have locally advanced or metastatic disease at initial clinical presentation. Non-small cell lung cancer (NSCLC) is a heterogeneous disease with a wide diversity of genomic subtypes in which mutations or abnormal gene expression profiles drive cancer cell growth. The ASPiRATION study will evaluate the clinical impact of CGP on the management of mNSCLC and assess the feasibility of implementation of CGP nationally. The study will be discussed and expected commencement and timelines.
Discovery of Epigenetic Field Cancerization and its Clinical Translation
PastWebinar
Mar 11
Discovery of Epigenetic Field Cancerization and its Clinical Translation
Mar 11, 2021
Many types of adult cancers are induced by chronic inflammation. Chronic inflammation is known to accelerate age-related methylation, and also induce aberrant DNA methylation of unique genomic regions. Mechanistically, TET expression was down-regulated by increased expression of multiple miRNAs due to NF-κB activation, and DNMT activity was increased by exposure to nitric oxide. Simultaneous TET down-regulation and DNMT activation induced strong aberrant DNA methylation, while either event induced only minimal aberrant DNA methylation. In this webinar, Dr. Ushijima will share his experience on how to find novel truths from unwanted or garbage data, and to bring basic findings to clinical applications.
What’s new in DRAGEN v3.8:
PastWebinar
Mar 19
What’s new in DRAGEN v3.8:
Mar 19, 2021
Learn about the latest DRAGEN features and improvements with the recent v3.8 release from Principal Engineer, Shyamal Mehtalia. Major highlights include the introduction of DRAGEN ORA compression technology which enables rapid, lossless compression of FASTQ files, translating in up to 80% savings on storage costs. We also expand our targeted callers and biomarker capabilities with the introduction of TMB and MSI as well as HLA typing. Additional features and improvements include generalized hardware accelerated trimming, expansion of the graph genome capabilities, and speed and accuracy improvements. BaseSpace users will be excited to see the introduction of DRAGEN DNA Amplicon and DRAGEN Single Cell RNA Apps.
Building a single cell and spatial tumor immune atlas for precision oncology
PastWebinar
Mar 25
Building a single cell and spatial tumor immune atlas for precision oncology
Mar 25, 2021
Register for our 03/25 joint live webinar with 10X Genomics/Illumina to learn more about the tumor immune microenvironment using single cell and spatial transcriptomics.
Introduction to Local Run Manager v3 with MiSeq Control Software v4
PastWebinar
Mar 26
Introduction to Local Run Manager v3 with MiSeq Control Software v4
Mar 26, 2021
Please join us for an introduction to Local Run Manager v3, the Windows-based software solution for run management and data analysis. This new version of the software will be launched along with the MiSeq Windows 10 update and MiSeq Control Software version 4.
Genomics Facilitates 5G Speed in Pepper (Capsicum spp.) Breeding
PastWebinar
Mar 30
Genomics Facilitates 5G Speed in Pepper (Capsicum spp.) Breeding
Mar 30, 2021
In this webinar, Professor Byoung-Cheorl Kang from the Department of Plant Science at Seoul National University will discuss how molecular markers for major traits are an essential tool to expedite the development of new varieties in pepper. Genome sequence assemblies for three Capsicum species have been developed by the short-read sequencing and are available for genetic study and molecular breeding. He will share how his team demonstrated the utility of the Dempsey genome by performing quantitative trait locus (QTL) and genome-wide association study (GWAS) analyses for multiple quantitative traits. The high-quality and chromosome-scale of the Dempsey genome provides a powerful new genomic resource for genetic analysis and genome-assisted breeding for pepper improvement.
RNA-Seq Virtual Program - Applications, Sample Preparation & Data Analysis
PastWebinar
Apr 14
RNA-Seq Virtual Program - Applications, Sample Preparation & Data Analysis
Apr 14, 2021
RNA sequencing (RNA-seq) is a highly sensitive and accurate method for measuring expression across the transcriptome and is one of the most cited NGS method. This method allows researchers to detect both known and novel features in a single assay. It also enables the detection of transcript isoforms, gene fusions, single nucleotide variants, and other features without the limitation of prior knowledge about the transcriptome. The Illumina team invites you to register for the free RNA Sequencing Program in Singapore.
Introduction to Sequencing by Synthesis (SBS)
PastWebinar
Apr 15
Introduction to Sequencing by Synthesis (SBS)
Apr 15, 2021
Illumina next-generation sequencing technology allows for massive parallel sequencing. Illumina Technical Support invites you to join us for a presentation and discussion on sample preparation, cluster generation and sequencing by synthesis chemistry. This webinar is targeted to those new to next-generation sequencing and will discuss the following topics: Illumina library construction, cluster generation methods by platform, sequencing by synthesis, and multiplexing and primary analysis.
Advances in Biology Webinar Series: Spatial Biology
PastWebinar
Apr 22
Advances in Biology Webinar Series: Spatial Biology
Apr 22, 2021
The vast complexities of biology require approaches to build a complete picture, starting from single cells to tissues and beyond. In this webinar series, we seek to showcase the latest Advances in Biology, and dive deep into the techniques and stories presented by experts in their field. For this episode, join us and explore how spatial technologies can advance your research.
Leveraging Multi-Omic Approaches to Understand Disease Stem Cells in Myeloid Malignancies
PastWebinar
Apr 28
Leveraging Multi-Omic Approaches to Understand Disease Stem Cells in Myeloid Malignancies
Apr 28, 2021
In this webinar, Stephen Chung, MD, of the University of Texas Southwestern Medical Center will discuss his team’s efforts to overcome this limitation by identifying cell surface markers present on clonal HSCs that will allow them to prospectively purify them for further functional and molecular studies. Towards this end, Mission Bio’s Tapestri single-cell multi-omics platform has made possible the correlation of cell surface phenotype with genotype with unprecedented resolution and throughput. Dr. Chung will present some of his team’s prior work describing cell surface markers aberrantly expressed on disease stem cells in MDS and AML, as well as some preliminary data utilizing the Mission Bio Tapestri single-cell multi-omics platform to identify novel disease stem cell associated markers.
Dysregulation of Histone Acetylation in Alzheimer’s Disease
PastWebinar
May 19
Dysregulation of Histone Acetylation in Alzheimer’s Disease
May 19, 2021
Interest in the field of epigenetics has increased rapidly over the last 15 years. So far, methylation analysis has been the most studied type of epigenetic regulation. Other, less studied mechanisms of regulation include non-coding RNA and histone modifications.
Epigenetic and Proteomic Predictors of Disease
PastWebinar
May 19
Epigenetic and Proteomic Predictors of Disease
May 19, 2021
Genome-wide association studies (GWAS) have associated over 40 loci with Alzheimer’s disease and recently, epigenome-wide association studies (EWAS) have highlighted neuropathology-associated DNA methylation differences for this disease. However, molecular mechanisms of gene regulations are complex and still not fully understood and integrating genomic, epigenomic and proteomic data can shed light on the biological mechanisms and improve disease risk prediction.
Multi-omics Analysis of Muscle Biopsies Identifies Genes Associated with Insulin Resistance
PastWebinar
May 19
Multi-omics Analysis of Muscle Biopsies Identifies Genes Associated with Insulin Resistance
May 19, 2021
Insulin-resistance is associated with obesity and type-2 diabetes. It is caused by a combination of environmental and genetic factors. The study of gene regulation can help understand how biological mechanisms are disrupted in the relevant tissues and potentially identify new markers of the disease to develop therapies in the future.
Introduction to Illumina DesignStudio
PastWebinar
May 20
Introduction to Illumina DesignStudio
May 20, 2021
Have a targeted sequencing project in mind? This webinar is targeted toward new and intermediate users looking to design a custom targeted sequencing assay in DesignStudio. We will show you how to use the software, and share tips and tricks to create a design for AmpliSeq for Illumina, Illumina DNA Prep with Enrichment, and TruSeq Targeted RNA Expression.
Virtual Seminar: Singapore Single-Cell Network (SSCN) Meeting May 2021
PastWebinar
May 21
Virtual Seminar: Singapore Single-Cell Network (SSCN) Meeting May 2021
May 21, 2021
In the last few years, single-cell technologies have revolutionized how we study biological processes, allowing unprecedented resolution and scale. SSCN is a community for all researchers in Singapore working in single-cell research, wetlab scientists and bioinformaticians with diverse interests from developmental biology to cancer research.
A Guide to Diet-Microbiome Study Design
PastWebinar
May 31
A Guide to Diet-Microbiome Study Design
May 31, 2021
Learn to design microbiome studies that maximize power and chances of success within a given research budget
Novel design of imputation-enabled SNP arrays for dual hybridization of wheat and barley
PastWebinar
Jun 16
Novel design of imputation-enabled SNP arrays for dual hybridization of wheat and barley
Jun 16, 2021
Array-based SNP genotyping platforms have low genotype error and missing data rates compared to genotyping-by-sequencing technologies.
Revolutionizing your research with single-cell multi-omics
PastWebinar
Jun 17
Revolutionizing your research with single-cell multi-omics
Jun 17, 2021
Date: 17nd June 2021, Thursday Time: 03:00 pm - 05:00 pm (Seoul)
Illumina and the Post-TruSeq World
PastWebinar
Jun 21
Illumina and the Post-TruSeq World
Jun 21, 2021
Within the past 12 months, Illumina launched a new Post-TruSeq world with the introduction of low cost, high performance enzymatic-based workflows, aimed at accelerating research while lowering the cost of sample preparation. As part of this launch, AGRF benchmarked the new Illumina Stranded mRNA, Illumina Stranded Total RNA with RiboZero Plus and Illumina DNA Prep PCR-Free library preparation kits to assess their performance with the aim of bringing these new generation services to our clients. AGRF continuously strives to introduce cutting-edge services to the market and this presentation will discuss the significant performance improvements these workflows have introduced.
Introduction to key concepts in Illumina sequencing data analysis
PastWebinar
Jun 22
Introduction to key concepts in Illumina sequencing data analysis
Jun 22, 2021
This Next-Generation Sequencing (NGS) bioinformatics tutorial covers data analysis approaches and considerations for experimental design. It will be an introduction of general concepts that can be applied to Illumina sequencing data as well as sequencing data and data analysis in general.
Total Transcriptomic Takeover: Charting the immune response against cancer to discover key cell types and predictive biomarker
PastWebinar
Jun 24
Total Transcriptomic Takeover: Charting the immune response against cancer to discover key cell types and predictive biomarker
Jun 24, 2021
Spatial Transcriptomics is a dynamic new field that is delivering spatially resolved transcriptome-wide profiling across a variety of tissue types and samples. NanoString is excited to announce Total Transcriptome Takeover together with Illumina-an event highlighting the use of spatial transcriptomics in cancer, immunology, and genetic diseases.
[iBric Webinar] 암 미세환경에 대한 공간전사체 분석
PastWebinar
Jun 29
[iBric Webinar] 암 미세환경에 대한 공간전사체 분석
Jun 29, 2021
암 유전체연구를 통해 암발생 및 전이에 관련된 유전체 및 전사체 수준 분석결과로부터 암 발생을 유도하는 돌연변이를 타겟으로 표적항암제 개발이 가능하게 되었다. 단일세포 수준에서 유전체를 분석할 수 있게 되면서 암세포와 면역세포를 포함한 암 미세환경세포에 대한 구성을 알게 되었고, 이를 통해 면역항암치료 효과를 높일 수 있게 되었다. 최근에는 암조직 병리 슬라이드에서 전사체 수준에서 분석할 수 있는 기술이 소개되면서 공간상에서 세포의 분포와 세포간 상호작용을 볼 수 있게 되었다. 이를 통해 암 미세환경을 구성하는 세포의 정확한 역할을 이해함으로써 새로운 치료법의 개발이 가능할 것으로 예상된다.
Building global startups – advancing breakthrough applications in genomics
PastWebinar
Jul 06
Building global startups – advancing breakthrough applications in genomics
Jul 6, 2021
Join the Illumina Accelerator and four global genomics startups in the biotech, clinical and agricultural industries to discuss key trends in the entrepreneurship and genomic spaces, how to build a genomics startup from ideation to commercialization, access capital and how to navigate and find opportunity in the current challenging times.
Metagenomics Part I: Introduction to Library Preparation and Sequencing
PastWebinar
Jul 14
Metagenomics Part I: Introduction to Library Preparation and Sequencing
Jul 14, 2021
Part 1 of a 2-part Metagenomics Webinar series discussing the end-to-end workflow for a metagenomics sequencing project.
Integrating Functional Information into Genome-wide Mapping and Prediction of Cattle Traits
PastWebinar
Jul 19
Integrating Functional Information into Genome-wide Mapping and Prediction of Cattle Traits
Jul 19, 2021
Understanding how DNA mutations change phenotypes is a central research topic in biology. This can also be said for genome-wide DNA markers, which can be used to predict phenotype and allows for better treatment of patients and genomic selection in agriculture.
Multiple Somatic Mutations Synergize to Drive Cerebral Cavernous Malformations
PastWebinar
Jul 28
Multiple Somatic Mutations Synergize to Drive Cerebral Cavernous Malformations
Jul 28, 2021
In this webinar, Daniel Snellings from the Duke University Medical Centre shares the role of somatic mutations in the pathogenesis of vascular malformations with specific focus on Cerebral Cavernous Malformations, Hereditary Hemorrhagic Telangiectasia, and Sturge-Weber Syndrome. The goal of his work is to identify novel somatic mutations, understand the genetic mechanisms by which these mutations arise, and evaluate how these mutations interact with existing genetic variation to drive malformations.
Illumina DRAGEN v3.9: Multi-Cloud support, new biomarkers and accuracy improvements
PastWebinar
Aug 11
Illumina DRAGEN v3.9: Multi-Cloud support, new biomarkers and accuracy improvements
Aug 11, 2021
Learn about the latest DRAGEN features and enhancements with the v3.9 release.
Conservation in the Age of Genomics
PastWebinar
Aug 17
Conservation in the Age of Genomics
Aug 17, 2021
In this webinar, Dr. Carolyn Hogg will discuss global genome initiatives which have been established to combat this and the genomic resources created for all eukaryotic life on earth. Although a reference genome does not conserve a species. Having the reference genome allows us to develop a suite of tools to understand both genome-wide and functional diversity within and between species. Conservation practitioners can then use these genetic resources to inform their decision-making. Currently, a gap in our applied knowledge exists between when genomes are produced, and the information that is used by conservation practitioners. In May 2020, Dr. Hogg and team launched the Threatened Species Initiative. Bringing together genome biologists, population biologists, bioinformaticians, population geneticists and ecologists with conservation agencies across Australia, including government, zoos and NGOs.
Advances in Biology: Single-Cell Multiomics
PastWebinar
Aug 17
Advances in Biology: Single-Cell Multiomics
Aug 17, 2021
The vast complexities of biology require approaches to build a complete picture, starting from single cells to tissues and beyond. In this webinar series, we seek to showcase the latest Advances in Biology, and dive deep into the techniques and stories presented by experts in their field. For this episode, join us and explore how single cell multiomics can advance your research.
Illumina DNA PCR-free Prep, Tagmentation: Introduction
PastWebinar
Aug 25
Illumina DNA PCR-free Prep, Tagmentation: Introduction
Aug 25, 2021
Illumina Technical Support invites you to join us for an introductory presentation on the library prep kit: Illumina® DNA PCR-Free Prep, Tagmentation. This webinar is geared towards new and intermediate users with a basic knowledge of next generation sequencing, and will discuss the following topics: the advantages of Illumina DNA PCR-free prep, tagmentation, the library workflow, tips for a successful library prep, and sequencing considerations.
It's NIPT Time! Whole-Genome Sequencing, a Technique without Borders
PastWebinar
Aug 27
It's NIPT Time! Whole-Genome Sequencing, a Technique without Borders
Aug 27, 2021
The introduction of cell-free DNA based prenatal screening (NIPT) in 2011 led to a huge improvement in specificity of prenatal screening for the three most frequent chromosomal aneuploidies (trisomies 21, 18 and 13) and also improved their detection rates. This enabled a vast reduction in number of post-screening counselling consultations and invasive test procedures. National Screening Programs are in place in a number of European countries. Some countries offer NIPT to all pregnant women and other countries offer NIPT as a secondary test to women with an elevated risk based on first trimester combined test results or other risk indicating parameters. Targeted NIPT technologies allow to test for the most frequent aneuploidies and eventually selected microdeletions. Whole-Genome Sequencing (WGS) based NIPT to the contrary allows to also report on aneuploidies on the other chromosomes and on large partial deletions and duplications, also called copy number variations (CNVs). Paired end sequencing is an important feature of WGS-based NIPT because it allows for more efficient alignment of fragments on the reference genome and because it adds to the parameters for measuring fetal fraction (FF). The ability to measure FF is an important quality parameter and should be a factor in choosing an NIPT provider. Reporting chromosome anomalies beyond the three most frequent aneuploidies allows detection of additional fetal anomalies, even in the absence of ultrasound anomalies. Second, it helps identify at risk pregnancies that can benefit from altered management. Third, it can take away the uncertainty related to unexplained adverse outcomes such as miscarriage and allows for better recurrence risk counselling. Finally, it will promote understanding of the effect of confined placental mosaicism on fetal health and wellbeing.
Virtual Seminar: Singapore Single-Cell Network (SSCN) Meeting September 2021
PastWebinar
Sep 09
Virtual Seminar: Singapore Single-Cell Network (SSCN) Meeting September 2021
Sep 9, 2021
In the last few years, single-cell technologies have revolutionized how we study biological processes, allowing unprecedented resolution and scale. SSCN is a community for all researchers in Singapore working in single-cell research, wetlab scientists and bioinformaticians with diverse interests from developmental biology to cancer research.
Leveraging a Cloud Ecosystem for Advanced Genomic Data Analysis
PastWebinar
Sep 22
Leveraging a Cloud Ecosystem for Advanced Genomic Data Analysis
Sep 22, 2021
Introducing Illumina Connected Analytics (ICA), our latest informatics product
Applications of single-cell multi-omics techniques in molecular biology, genetics and cancer research
PastWebinar
Sep 22
Applications of single-cell multi-omics techniques in molecular biology, genetics and cancer research
Sep 22, 2021
Emerging single-cell multi-omics sequencing technologies allow the capture of multiple modalities from a cell
NovaSeq 6000 Run Quality and Best Practices
PastWebinar
Sep 24
NovaSeq 6000 Run Quality and Best Practices
Sep 24, 2021
Join llumina Technical Support for a discussion on the NovaSeq™ 6000 Sequencing System. This webinar aims to empower NovaSeq™ 6000 users to work through unexpected situations that may arise during run set up and run performance. We will introduce NovaSeq™ 6000 Sequencing System users to resources that will aide in resolving these situations.
Development and Implementation of Genomic Selection in Pulse Crops
PastWebinar
Sep 28
Development and Implementation of Genomic Selection in Pulse Crops
Sep 28, 2021
In this webinar, Dr. Kaur will describe recent advances in the integration of genomic predictions in pulse pre-breeding (chickpea) and breeding (lentil and field pea). Building on 10+ years of historical data in lentil and field pea breeding, genomic prediction equations for key breeding traits including yield, seed weight, size and protein content, and multiple abiotic and biotic stress tolerances have been derived with moderate to high prediction accuracies (0.3-0.8). Genomic estimated breeding values, selection indices and crossing schemes designed using optimal parental combinations have been delivered to breeders. Stochastic computer simulations investigating the benefit of GS optimization strategies for disease resistance, grain weight and yield in multiple environments with different levels of genotype-by-environment interactions have indicated increased genetic gain per unit of time compared to phenotypic selection.
Overview of Illumina’s newest instrument, the NextSeq1000/2000 [Korean]
PastWebinar
Sep 29
Overview of Illumina’s newest instrument, the NextSeq1000/2000 [Korean]
Sep 29, 2021
This webinar is designed to help customers become familiar with the NextSeq 1000/2000 platform. This webinar will cover - features of the NextSeq 1000/2000, specifications, end to end workflow, library preparation considerations, guidance on run analysis, and tips and best practices.
Sequencing Analysis Viewer (SAV): A Beginner's Guide
PastWebinar
Oct 13
Sequencing Analysis Viewer (SAV): A Beginner's Guide
Oct 13, 2021
Please join us for an introductory presentation to Sequencing Analysis Viewer (SAV). This software is an application to view important quality metrics generated during sequencing runs. This webinar will provide a guided tour for beginners on how to use SAV, as well as tips and tricks for reviewing the most useful information for sequencing runs. This webinar is targeted at new users and will go over the following topics: How to load data into SAV, what metrics are available in each tab of the software and understanding which are the most valuable metrics for run review and where to find them.
Clonal Heterogeneity in Acute Lymphoblastic Leukemia at diagnosis and during chemotherapy treatment detected by single-cell sequencing
PastWebinar
Oct 21
Clonal Heterogeneity in Acute Lymphoblastic Leukemia at diagnosis and during chemotherapy treatment detected by single-cell sequencing
Oct 21, 2021
Dr. Cools will discuss how single-cell DNA amplicon sequencing is a sensitive assay to detect clonal architecture and evolution of the malignant cells in ALL, and present his findings published in the Blood paper, “Single-cell DNA amplicon sequencing reveals clonal heterogeneity and evolution in T-cell acute lymphoblastic leukemia”.
Troubleshooting Infinium Genotyping Data [Korean]
PastWebinar
Oct 27
Troubleshooting Infinium Genotyping Data [Korean]
Oct 27, 2021
This webinar is designed to help customers troubleshoot Infinium Genotyping Data. This webinar will cover- Specs and basic steps of data QC, the Infinium genotyping assay workflow and troubleshooting tools.
Unravelling immune complexities using Single Cell Multi-omics
PastWebinar
Nov 11
Unravelling immune complexities using Single Cell Multi-omics
Nov 11, 2021
Join us for a day of deep science using single cell multiomics technology, as scientists across Asia dive into the complexities of breast cancer, obesity, immune related adverse events, and CAR-T cell therapy!
The case studies of the Illumina NextSeq 2000 system in microbiology [Korean]
PastWebinar
Nov 16
The case studies of the Illumina NextSeq 2000 system in microbiology [Korean]
Nov 16, 2021
The Sanigen provides service for WGS, shotgun metagenomics and bacterial transcriptome sequencing in bacteria samples using NextSeq 2000. In this presentation, we will introduce the performed Sanigen’s service with NextSeq 2000 in 2021.
Interim Results from the Endoscopic Ultrasound Molecular Evaluation of Pancreatic Cancer (EU ME PC) Trial
PastWebinar
Nov 16
Interim Results from the Endoscopic Ultrasound Molecular Evaluation of Pancreatic Cancer (EU ME PC) Trial
Nov 16, 2021
The EU ME PC trial is a multi-center study examining the utility of Endoscopic Ultrasound FNA to provide tissue for comprehensive molecular profiling of pancreatic cancer for patients with metastatic, locally advanced or recurrent pancreatic cancer.
Genomic Surveillance Solutions for COVID & Beyond
PastWebinar
Nov 17
Genomic Surveillance Solutions for COVID & Beyond
Nov 17, 2021
Since its emergence in China, SARS-CoV-2 has spread worldwide, challenging our health care systems, economies, and societies at an unprecedented scale. During this pandemic, Next Generation Sequencing ‘NGS’ based whole genome sequencing of SARS-CoV-2 has played a critical role in the global Public Health response. Global-scale NGS based whole genome sequencing enabled identification and tracking of novel virus variants with increased transmissibility and/or morbidity (“Variants of Concern”), detection of signature erosion in PCR assays and allowed post-market monitoring of vaccines and mAb therapies. As of today, global databases contain over 3 million SARS-CoV-2 genome submissions, representing one of the largest public health collaborations in infectious disease genomics, cementing NGS as an essential tool in outbreak management and future preparedness for pandemic threats. Illumina hybrid-capture and amplicon based end-to-end NGS workflows with streamlined variant calling have been deployed in both centralized sequencing ‘hubs’ as well as de-centralized sites enabling low, middle and high-income countries to participate in the global response. Current workflows are applied for sequencing clinical samples, but novel emerging applications critical to the pandemic response incorporate NGS based approaches, such as wastewater-based population monitoring or host-response profiling to predict potential disease outcome. The global response to COVID-19 is catalyzing the development of a global pathogen genomics surveillance ecosystem for early detection and management of emerging and re-emerging pathogens, as well as Antimicrobial Resistance determinants with pandemic potential. The frequency of infectious disease outbreaks has increased in recent years, driven by globalization of our society, urbanization, and population growth, facilitating zoonotic spillover events of viruses and multidrug resistant bacteria from animals to humans. The impact of genomic surveillance on the response to the over 12,000 Infectious Disease outbreaks reported by WHO since 1980 has thus far not been realized at its full potential.
Redefining NGS in Cancer Research
PastWebinar
Nov 30
Redefining NGS in Cancer Research
Nov 30, 2021
NGS can now be used to characterize the proteome, epigenome, non-coding RNAs, and even small RNAs.
Empowering Precision Oncology through Genomics in India
PastWebinar
Dec 04
Empowering Precision Oncology through Genomics in India
Dec 4, 2021
Healthcare Global Enterprises Ltd (HCG), India’s largest provider of cancer care, is at the forefront of the battle against cancer. Through its network of 23 comprehensive cancer centers, spread across India, HCG has brought advanced cancer care to the doorstep of millions of people. Join us for this webinar co-organised by HCG - The Specialist In Cancer Care, Illumina Inc and Premas Life Science where thought leaders will share their experience of the clinical utility of genomics in precision oncology. The purpose of this webinar is to raise awareness of what is possible in oncology, and how this will benefit patients.
Improving care for critically ill infants with whole-genome sequencing
PastWebinar
Dec 15
Improving care for critically ill infants with whole-genome sequencing
Dec 15, 2021
Does whole-genome sequencing (WGS) of critically ill infants improve their care?
Establishing a Pharmacologic Service for Routine Clinical Care
PastWebinar
Dec 21
Establishing a Pharmacologic Service for Routine Clinical Care
Dec 21, 2021
Adverse drug reactions (ADRs) are responsible for ~5% of hospital admissions, and occur during 6-15% of hospital stays. Approximately 30% are caused by drugs with a known major clinically significant pharmacogenomics variant, as much as 30% of adverse drug-related admissions may be predictable – and thus preventable - by pharmacogenomics (PGx) testing. In this talk, we will discuss the introduction of pharamacogenomics testing into particular clinical settings where it is likely to be particularly clinically relevant. Our project’s goal is to provide pre-emptive rather than reactive testing in these clinical settings by using rapid genomic technologies and information management integrated into the hospital electronic medical record. This vision requires development of a PGx knowledge centre and a clinical support database as well as the validation of new technologies to improve cost effective PGx measurements. This talk will focus on implementation of these goals as well as the challenges of introducing new genomic testing into routine clinical care.
Introduction: BaseSpace Sequence Hub
PastWebinar
Dec 23
Introduction: BaseSpace Sequence Hub
Dec 23, 2021
BaseSpace Sequence Hub is a genomics cloud computing platform designed to bring simplified data management and analytical sequencing tools directly to investigators in a user-friendly format. BaseSpace Sequence Hub provides flexibility and convenience with an array of tools, significantly expanding the possibilities of yielding meaningful results from NGS data. This webinar provides introduction to Basespace Sequence Hub and how to use followed by introduction to common analysis workflows.
Illumina Options for SARS-CoV-2 / COVID-19 Epidemiology
PastWebinar
Feb 09
Illumina Options for SARS-CoV-2 / COVID-19 Epidemiology
Feb 9, 2022
An overview of Illumina’s end-to-end Illumina workflows to capture the complete genome sequence of SARS-CoV-2
National Wastewater Surveillance System
PastWebinar
Feb 09
National Wastewater Surveillance System
Feb 9, 2022
An overview of the CDC’s National Wastewater Surveillance System
Wastewater-Based Epidemiology (WBE) and Next-Generation Sequencing (NGS)
PastWebinar
Feb 09
Wastewater-Based Epidemiology (WBE) and Next-Generation Sequencing (NGS)
Feb 9, 2022
A discussion of the expanding field of wastewater-based epidemiology (WBE)
Illumina sequencing for Wastewater-Based Surveillance (WBE)
PastWebinar
Feb 09
Illumina sequencing for Wastewater-Based Surveillance (WBE)
Feb 9, 2022
A high-level overview of why wastewater surveillance is of interest to us now.
Sewers: Understanding the Impact on Samples
PastWebinar
Feb 09
Sewers: Understanding the Impact on Samples
Feb 9, 2022
Essential background that explains critical aspects of wastewater surveillance.
Considerations for Wastewater-Based Epidemiology NGS Data Analysis
PastWebinar
Feb 09
Considerations for Wastewater-Based Epidemiology NGS Data Analysis
Feb 9, 2022
Important considerations when working with wastewater-based epidemiology (WBE) sample types
Wastewater-Based Epidemiology NGS Data Demonstration
PastWebinar
Feb 09
Wastewater-Based Epidemiology NGS Data Demonstration
Feb 9, 2022
A data analysis demonstration looking at sets of nasal swab and wastewater samples
SARS-CoV-2 Genomic Surveillance in India: One Year and Counting
PastWebinar
Feb 17
SARS-CoV-2 Genomic Surveillance in India: One Year and Counting
Feb 17, 2022
India has carried a heavy burden during the COVID-19 pandemic and has recorded the second largest volume of COVID-19 cases. To address the COVID-19 crisis, India adopted genomics-based surveillance of the virus, which has been deployed across various initiatives including the Indian SARS-CoV2 Genomics Consortium (INSACOG). In this webcast, Dr. Sridhar Sivasubbu, CSIR-IGIB will explain the critical role of genomic surveillance in managing the COVID-19 pandemic in India.
Critical evaluation of Illumina Mouse Methylation Array and comparison with RRBS in murine colorectal cancer models
PastWebinar
Feb 17
Critical evaluation of Illumina Mouse Methylation Array and comparison with RRBS in murine colorectal cancer models
Feb 17, 2022
DNA methylation is a common epigenetic modification that can alter gene expression. As DNA methylation is a genomic phenomena, accurate assessment of the DNA methylation landscape requires genome-scale tools. Genomic-scale profiling of model organisms, including mice, has traditionally been limited to sequencing-based methods. Illumina has recently developed a DNA methylation array specific to the murine samples, capturing DNA methylation information for >250,000 CpG sites. In this webinar, Dr Fennell will discuss his impressions of the technology and present the results of a comparative analysis between the Illumina Mouse Methylation Array and Reduced Representation Bisulphite Sequencing in two models of colorectal cancer.
Infinium Array: Best Practices
PastWebinar
Feb 25
Infinium Array: Best Practices
Feb 25, 2022
Optimize Infinium data quality by following these Infinium Best Practices. For new and experienced users, this webinar will touch on all aspects of the Infinium workflow: Lab Setup and Maintenance, Lab tracking, Infinium assay tips and data management.
Are lower-middle-income countries ready to sequence mycobacterium tuberculosis?
PastWebinar
Mar 04
Are lower-middle-income countries ready to sequence mycobacterium tuberculosis?
Mar 4, 2022
Mycobacterium tuberculosis (MTB) is the world's top infectious killer, and the growing prevalence of drug-resistant TB poses formidable challenges in controlling this disease. Universal access to comprehensive drug susceptibility testing (DST) is a key component of the WHO End-TB strategy. In this talk, Dr. Camila will share from the point of view of a clinician and clinical microbiologist, the impact of NGS in supporting MTB treatment and patient management, and what is needed to bring the next-generation TB care closer to patients.
Illumina DRAGEN v3.10: Setting New Standards for Data Accuracy, and more
PastWebinar
Mar 11
Illumina DRAGEN v3.10: Setting New Standards for Data Accuracy, and more
Mar 11, 2022
Tune in to our upcoming webinar to learn about the latest DRAGEN release – DRAGEN v3.10. This release brings exciting new advancements including; significant germline small variant accuracy improvements with DRAGEN Graph and Illumina Machine Learning, enhanced comprehensiveness with RNA Amplicon support, a targeted GBA caller, and MHC graph reference improvements, and population genomics scalability improvements.
Secrets to Success with Single-Cell Multiomics
PastWebinar
Mar 17
Secrets to Success with Single-Cell Multiomics
Mar 17, 2022
In the 'Secrets to Success with Single-Cell Multiomics' session, you will hear from leading experts in single-cell multiomics. They will share with you their experiences in implementing multiomic approaches and how they have found success. Panelists will cover which methods are being combined most often, the most common issues they have encountered with samples and experiments, and their favourite ways of visualizing data.
NextSeq 1000/2000: Introduction
PastWebinar
Mar 18
NextSeq 1000/2000: Introduction
Mar 18, 2022
Illumina Technical Support invites you to join us for a discussion of the new NextSeq 1000/2000 platform. This webinar is designed to help customers become familiar with the NextSeq 1000/2000 platform. This webinar will cover: features of the NextSeq 1000/2000, specifications, end to end workflow, library preparation considerations, guidance on run analysis, and tips and best practices.
Spatiotemporal analysis of cardiac tissue during myocardial infarction
PastWebinar
Mar 23
Spatiotemporal analysis of cardiac tissue during myocardial infarction
Mar 23, 2022
10x Genomics and Illumina are excited to co-host a webinar featuring William Boisvert and Jonathan Yap from theUniversity of Hawaii
Homegrown Genomes - Realizing the Benefits of "Locally-Sourced" Genomes
PastWebinar
Mar 24
Homegrown Genomes - Realizing the Benefits of "Locally-Sourced" Genomes
Mar 24, 2022
Hear Matthew Bower's talk from ACMG 2022 on implementation of whole genome sequencing at the University of Minnesota Medical Center
Enabling in-house comprehensive genomic profiling for today's and tomorrow's clinical needs
PastWebinar
Mar 30
Enabling in-house comprehensive genomic profiling for today's and tomorrow's clinical needs
Mar 30, 2022
James P. Solomon of Weill Cornell Medicine describes considerations in choosing assays for implementation and will discuss the value of in-house comprehensive CGP assays.
Improving care for critically ill infants with whole-genome sequencing
PastWebinar
Apr 04
Improving care for critically ill infants with whole-genome sequencing
Apr 4, 2022
Does whole-genome sequencing (WGS) of critically ill infants improve their care?
ECCMID 2022 Symposium
PastWebinar
Apr 23
ECCMID 2022 Symposium
Apr 23, 2022
Five presentations dedicated to exploring the benefits of NGS for studying viruses and pathogens, beyond COVID.
Can genomic surveillance detect the next pandemic before it’s too late?
PastWebinar
Apr 26
Can genomic surveillance detect the next pandemic before it’s too late?
Apr 26, 2022
The speakers in this webinar will discuss the current state of infectious disease surveillance, its strengths, and shortcomings.
Leveraging sequencing technologies for cardiovascular research and precision medicine
PastWebinar
Apr 26
Leveraging sequencing technologies for cardiovascular research and precision medicine
Apr 26, 2022
Victoria Parikh and Muredach Reilly discuss how genome sequencing and omics approaches are paving the way for precision cardiovascular medicine.
MiSeq: Run Quality and Best Practices
PastWebinar
Apr 27
MiSeq: Run Quality and Best Practices
Apr 27, 2022
Illumina Technical Support invites users to join us for a discussion of the MiSeq system. The MiSeq System offers integrated cluster generation, amplification, sequencing, and data analysis into a single instrument. This webinar will go through troubleshooting considerations at each of these steps and is targeted toward new and intermediate users with a basic understanding of the Illumina sequencing workflow and the Sequence Analysis Viewer (SAV) software. We will cover the following topics: run setup and start best practices, assessment of runs in progress using SAV, and tips and best practices.
Advancements in translational biomarker identification from cell-free RNA
PastWebinar
May 03
Advancements in translational biomarker identification from cell-free RNA
May 3, 2022
Learn about the newest Illumina cell-free RNA sequencing methods
Introducing Illumina Infinity long read technology
PastWebinar
May 09
Introducing Illumina Infinity long read technology
May 9, 2022
Join us to learn about the power of Infinity long reads.
Sequencing Considerations for Low Diversity Samples
PastWebinar
May 11
Sequencing Considerations for Low Diversity Samples
May 11, 2022
Nucleotide diversity is critical for optimal run performance and high-quality data generation. Low diversity libraries may skew software performance and data accuracy resulting in poor quality runs. We will discuss what is nucleotide diversity and why is it important. Topics will cover understanding of base imaging on Illumina sequencing platforms, strategies to optimize low diversity sequencing data, and overview of percentage base check and quality score calculation.
A New DNA Sequencing Technology for Animal Breeding and Research
PastWebinar
May 12
A New DNA Sequencing Technology for Animal Breeding and Research
May 12, 2022
A New Era for Commercial Breeders and Producers Begins with Sequencing-based Whole Genome and Genotyping Technology
A comprehensive solution for virtually any application:  NextSeq™ 1000 and 2000
PastWebinar
May 24
A comprehensive solution for virtually any application: NextSeq™ 1000 and 2000
May 24, 2022
Learn how the NextSeq™ 1000 and 2000 enables you to study gene expression of more targets in less time.
NextSeq 2000: Introduction to Analysis with DRAGEN
PastWebinar
May 31
NextSeq 2000: Introduction to Analysis with DRAGEN
May 31, 2022
This webinar is an overview of DRAGEN on our latest NextSeq1000/2000 instruments. We will discuss the functionality and new features of DRAGEN, software management, different analysis workflows. We will also discuss how to set up the analysis onboard the instrument and output generated by different analysis workflows.
Unlocking Precision Medicine: The Transformational Impact of CGP
PastWebinar
Jun 03
Unlocking Precision Medicine: The Transformational Impact of CGP
Jun 3, 2022
Fireside Chat among a panel of leading oncologists from select community and academic programs.
Extending the Reach of Illumina Sequencing Platforms
PastWebinar
Jun 07
Extending the Reach of Illumina Sequencing Platforms
Jun 7, 2022
An overview of efforts to scale and expand access to our next-generation sequencing platforms and introduce NextSeq 1000/2000 P1 100c & 600c kits
Emerging Applications and Advances in Whole-genome Sequencing
PastWebinar
Jun 08
Emerging Applications and Advances in Whole-genome Sequencing
Jun 8, 2022
An overview of the latest advances in Illumina's whole-genome offering and the vast potential of emerging genomics technologies.
Connecting Samples to Genomic Analysis and Interpretation
PastWebinar
Jun 09
Connecting Samples to Genomic Analysis and Interpretation
Jun 9, 2022
Mike Lelivelt discusses Illumina's end-to-end solution for connecting samples to critical genomic insights.
How to Use the Partek Flow Data Viewer
PastWebinar
Jun 12
How to Use the Partek Flow Data Viewer
Jun 12, 2022
Visually build powerful, interactive visualizations.
AGBT 2022 - Illumina announces next generation products and data
PastWebinar
Jun 15
AGBT 2022 - Illumina announces next generation products and data
Jun 15, 2022
In this live webinar, Anthony will present an overview of Illumina’s exciting announcements from AGBT 2022 including: Efforts to scale and expand access to lllumina's next-generation sequencing platforms; The latest advances in Illumina’s whole genome offering and the vast potential of emerging genomics technologies; and lllumina's end-to-end solution for connecting samples to critical genomic insights.
Single-cell transcriptomic landscape in Alzheimer’s disease
PastWebinar
Jun 16
Single-cell transcriptomic landscape in Alzheimer’s disease
Jun 16, 2022
A single-cell study of 380,000 nuclei in late-stage Alzheimer’s Disease (AD) using Parse Biosciences's whole transcriptome kit
GenomeStudio Genotyping: Evaluating Infinium Assay Controls
PastWebinar
Jun 17
GenomeStudio Genotyping: Evaluating Infinium Assay Controls
Jun 17, 2022
This webinar will focus on the Genotyping module of GenomeStudio for the analysis of Illumina microarrays/beadchips. The purpose, types, and uses of Infinium assay controls will be discussed, along with some tips to effectively evaluate Infinium controls.
DNA Methylation Dynamics and Dysregulation Delineated by High-Throughput Profiling in the Mouse
PastWebinar
Jul 01
DNA Methylation Dynamics and Dysregulation Delineated by High-Throughput Profiling in the Mouse
Jul 1, 2022
In this webinar, Peter W. Laird, professor at the Van Andel Research Institute, will discuss the development of a mouse DNA methylation array that contains 296,070 probes representing the diversity of mouse DNA methylation biology. Laird will present a comprehensive validation of this array platform and discuss the applications for comparative epigenomics, genomic imprinting, epigenetic inhibitors, PDX assessment, backcross tracing, and epigenetic clocks.
DNA methylation dynamics and dysregulation delineated by high-throughput profiling in the mouse
PastWebinar
Jul 01
DNA methylation dynamics and dysregulation delineated by high-throughput profiling in the mouse
Jul 1, 2022
In this webinar, Peter Laird discusses the development of a mouse DNA methylation array that contains 296,070 probes representing the diversity of mouse DNA methylation biology.
Genomics applied to livestock improvement
PastWebinar
Jul 06
Genomics applied to livestock improvement
Jul 6, 2022
Christine Couldrey discusses the use of high-throughput and array technologies in the breeding and health of dairy cattle.
Museum Genomics of Australia’s Native Rodents
PastWebinar
Jul 20
Museum Genomics of Australia’s Native Rodents
Jul 20, 2022
In this webinar, Dr. Kevin Rowe from Museums Victoria and Riley Ferguson from UOM discusses rodent diversity applying genomic tools to natural history specimens, including recent whole genome resequencing of two species of threatened Australian rodents genotyped using the DRAGEN™ pipeline. These genomic data are helping us understand the origin of species, the molecular basis of their ecological and functional diversity, and their response to human globalization over the past century.
Infinium Genotyping: Introduction to DesignStudio Microarray Assay Designer for Custom and Semi-Custom Infinium Genotyping Arrays
PastWebinar
Jul 29
Infinium Genotyping: Introduction to DesignStudio Microarray Assay Designer for Custom and Semi-Custom Infinium Genotyping Arrays
Jul 29, 2022
An introduction to the online DesignStudio Microarray Assay Designer; a tool that streamlines the process of designing fully or semi-custom Infinium iSelect HD, HTS, and XT format BeadChips. This webinar will focus on how to effectively create custom content assay designs as well as demonstrate the product ordering process using DesignStudio Microarray Assay Designer.
DRAGEN™ v4.0: Unlock the Full Potential of Genomics
PastWebinar
Aug 12
DRAGEN™ v4.0: Unlock the Full Potential of Genomics
Aug 12, 2022
Learn about the latest DRAGEN™ release – DRAGEN v4.0! Unlock the power of genomics with comprehensive secondary analysis - from single cell multiomics to pharmacogenomics applications to imputation – it’s all now available in one single platform. Expanded comprehensiveness paired with accuracy and efficiency improvements make DRAGEN 4.0 our most exciting release yet, paving the way for WGS secondary analysis at scale.
BaseSpace Sequence Hub: Introduction and Analysis Overview
PastWebinar
Aug 25
BaseSpace Sequence Hub: Introduction and Analysis Overview
Aug 25, 2022
In this webinar, we discuss how to navigate the BaseSpace dashboard, general BaseSpace functionally, and tips and tricks for successful application and workflow utilization. We will cover the following topics: how to upload/view data in BaseSpace, discussion of major analysis workflows, general overview of how to analyze data on BaseSpace.
Enabling Functional Profiling of Human Metatranscriptomes Using RiboZero™ Plus Microbiome
PastWebinar
Sep 01
Enabling Functional Profiling of Human Metatranscriptomes Using RiboZero™ Plus Microbiome
Sep 1, 2022
Enabling sensitive profiling of microbial diversity and metabolic activity.
Metatranscriptomic Analysis of the Skin and Gut Microbiomes of an Isolated Amazonian Community
PastWebinar
Sep 06
Metatranscriptomic Analysis of the Skin and Gut Microbiomes of an Isolated Amazonian Community
Sep 6, 2022
Discussion of the shift from using metagenomics to metatranscriptomics to understand the pathways driving health.
Blood-Based Comprehensive Genomic Profiling: From Validation to Clinical Studies
PastWebinar
Sep 20
Blood-Based Comprehensive Genomic Profiling: From Validation to Clinical Studies
Sep 20, 2022
Dr. Chris Karlovich shares key takeaways from the validation of an NGS-backed comprehensive genomic profiling (CGP) liquid biopsy assay.
The role of genomics for biodiversity conservation in a changing climate
PastWebinar
Sep 21
The role of genomics for biodiversity conservation in a changing climate
Sep 21, 2022
This on-demand webinar highlights how genomic technologies can shed light on the evolutionary history of Earth’s species and how we can best preserve them.
iSeq100: Run Quality and Best Practices
PastWebinar
Sep 22
iSeq100: Run Quality and Best Practices
Sep 22, 2022
Illumina Technical Support invites users to join us for a discussion of the iSeq100 system. This webinar is targeted to users of the iSeq 100 Sequencing System and we will discuss run review techniques and troubleshooting considerations specific to the iSeq 100.
Genomics for global health and pandemic preparedness
PastWebinar
Sep 28
Genomics for global health and pandemic preparedness
Sep 28, 2022
The COVID-19 pandemic launched a new era of infectious disease surveillance with a massive global increase in genomic sequencing infrastructure. Public health professionals collaborated with policymakers and enabled evidence-based public health decisions. Join us in this webinar and hear Darcy Whitlock, Illumina Senior Global Product Manager, share key NGS methodologies for critical public health and infectious disease surveillance needs.
The Illumina Innovation Roadmap: Empowering Genomic Breakthroughs
PastWebinar
Sep 29
The Illumina Innovation Roadmap: Empowering Genomic Breakthroughs
Sep 29, 2022
View video of the unveiling event to learn about product announcements and exciting updates on previously announced technologies.
Overview of single cell RNA sequencing for cell biologists
PastWebinar
Oct 06
Overview of single cell RNA sequencing for cell biologists
Oct 6, 2022
Overview of single cell RNA sequencing for cell biologists
Integrating Next-Generation Sequencing into Microbiology Clinical Research
PastWebinar
Oct 07
Integrating Next-Generation Sequencing into Microbiology Clinical Research
Oct 7, 2022
Arryn Craney, clinical microbiologist for Orlando Health, discusses integration options for next-generation sequencing in the microbiology clinical research laboratory
Discoveries in immunology at the single-cell level
PastWebinar
Oct 11
Discoveries in immunology at the single-cell level
Oct 11, 2022
In this webinar, we'll hear three talks that highlight advances made in distinct fields using single-cell sequencing technology.
Resolving tumor microenvironment heterogeneity at the single cell level from fixed samples
PastWebinar
Oct 20
Resolving tumor microenvironment heterogeneity at the single cell level from fixed samples
Oct 20, 2022
10x Genomics and Illumina will present the Single Cell Fixed RNA solution, which enables RNA sequencing at the single cell level.
Sequencing: How to Plan Your First Sequencing Project
PastWebinar
Oct 27
Sequencing: How to Plan Your First Sequencing Project
Oct 27, 2022
This Illumina Technical Support webinar discusses the end-to-end workflow for planning your first sequencing project. We will give an overview of the full sequencing process, from idea to data analysis whilst also including helpful resources along the way. This webinar is an introduction for new NGS users. We encourage you to share this webinar to those who may benefit from this NGS sequencing overview. We will discuss the following topics: Upfront sequencing considerations, Library preparation and Sequencing to data analysis.
Illumina Complete Long-Read technology: Detailed insights into complex genomes
PastWebinar
Oct 27
Illumina Complete Long-Read technology: Detailed insights into complex genomes
Oct 27, 2022
A discussion of the benefits of the Illumina Complete Long Read technology, including accuracy, scalability, and workflow improvements.
Enabling in-house comprehensive genomic profiling (CGP) to meet increasingly clinical oncology needs
PastWebinar
Nov 02
Enabling in-house comprehensive genomic profiling (CGP) to meet increasingly clinical oncology needs
Nov 2, 2022
Wojciech Swat of GenPath Diagnostics presents his experience in implementing comprehensive genomic profiling (CGP) in-house using a hybrid capture-based CGP assay and discuss its impact in clinical practice at GenPath Oncology.
Comprehensive Genomic Profiling from Liquid Biopsy Samples
PastWebinar
Nov 02
Comprehensive Genomic Profiling from Liquid Biopsy Samples
Nov 2, 2022
In this presentation, Illumina Associate Director of Medical Affairs, Alison Roos will discuss the rationale and drivers for the implementation of a CGP liquid biopsy assay to better support molecular testing and therapy matching.
Strandology Strand Designations In Illumina Manifests
PastWebinar
Nov 03
Strandology Strand Designations In Illumina Manifests
Nov 3, 2022
Illumina’s Manifests for our Infinium BeadChips contain different strand and allele designations, allowing for multiple ways to report genotyping alleles. In this webinar we will discuss the following topics: Illumina’s strand and allele designations contained in our manifests, and how they relate to standardized designations; how and why these designations were developed; examples of how to convert alleles reported from one strand designation to alleles based on another strand designation.
Future Proofing Health Systems: The role of genomics in pandemic preparedness, surveillance, and biosecurity
PastWebinar
Nov 09
Future Proofing Health Systems: The role of genomics in pandemic preparedness, surveillance, and biosecurity
Nov 9, 2022
Recorded at the World One Health Congress in Singapore in November, 2022, this expert panel discussion discusses the role of genomic surveillance in pandemic preparedness and what it means to have a genomics-powered public health surveillance and disease control system.
NovaSeq™ 6000: Run Quality and Best Practices
PastWebinar
Nov 16
NovaSeq™ 6000: Run Quality and Best Practices
Nov 16, 2022
Illumina Technical Support invites you to join us for a discussion on NovaSeq™ 6000 run quality and best practices. This webinar aims to empower NovaSeq™ 6000 users to work through unexpected situations that may arise during run set up and run performance. We will introduce NovaSeq™ 6000 Sequencing System users to resources that will aid in resolving these situations.
Introduction to BCL2FASTQ
PastWebinar
Nov 17
Introduction to BCL2FASTQ
Nov 17, 2022
Bcl2Fastq is a Linux-based software that converts base call files generated from an Illumina sequencing run to FASTQ files as well as demultiplex samples. This webinar focuses on Bcl2fastq v2+ and is targeted for new to intermediate users who are interested in the configurable options that this command line program allows. We will cover the following topics: requirements to run Bcl2Fastq, command line basics, commonly used options, frequently asked ‘How To….’ questions.
Genomics for global health and pandemic preparedness
PastWebinar
Nov 28
Genomics for global health and pandemic preparedness
Nov 28, 2022
A global surveillance system for infectious diseases is now possible as a result of the sequencing infrastructure built during the pandemic.
An Introduction to Illumina DNA PCR-Free Prep, Tagmentation
PastWebinar
Nov 29
An Introduction to Illumina DNA PCR-Free Prep, Tagmentation
Nov 29, 2022
The Illumina DNA PCR-Free Prep, Tagmentation library preparation kit is a new automation compatible whole-genome sequencing library prep kit. In this webinar, we will cover the following topics: library preparation workflow, library evaluation, quality control, next-generation sequencing considerations and analysis.
Infinium Best Practices
PastWebinar
Dec 01
Infinium Best Practices
Dec 1, 2022
Optimize Infinium data quality by following these Infinium Best Practices. For new and experienced users, this webinar will touch on all aspects of the Infinium workflow: lab setup and maintenance, lab tracking, Infinium assay tips, data management.
국내 연구자를 위한 RNA 시퀀싱 (RNA-Seq) 실험 기회 제공 프로그램
PastWebinar
Dec 15
국내 연구자를 위한 RNA 시퀀싱 (RNA-Seq) 실험 기회 제공 프로그램
Dec 15, 2022
RNA 시퀀싱(RNA sequencing, RNA-Seq)은 전사체(transcriptome) 전체에 걸쳐 유전자 발현(gene expression)을 측정하는 데 활용되는 민감도와 정확도가 높은 시퀀싱 방법으로, 가장 많이 인용되는 차세대 시퀀싱(next-generation sequencing, NGS) 방법 중 하나입니다. 연구자는 RNA-Seq을 통해 한 번의 assay로 알려진 특징과 새로운 특징을 모두 확인할 수 있을 뿐만 아니라, 전사체에 관한 사전 지식 없이도 동형 전사물(transcript isoform), 유전자 융합(gene fusion), 단일 염기서열 변이(single nucleotide variant, SNV) 및 기타 특징을 찾아낼 수 있습니다. 이와 관련해 일루미나 코리아에서는 무료 RNA-Seq 워크샵을 개최할 예정이오니 참석을 원하시면 아래 정보를 확인하신 후 신청해 주시기 바랍니다.
Local Run Manager v3 with MiSeq Control Software v4: Introduction
PastWebinar
Dec 16
Local Run Manager v3 with MiSeq Control Software v4: Introduction
Dec 16, 2022
This webinar focuses on Local Run Manager version 3; this is the new Windows-based software solution for run management and data analysis. Local Run Manager v3 replaces MiSeq Reporter, and this webinar introduces the features of Local Run Manager v3. The webinar will cover following topics: features of Local Run Manager v3, how to set up runs and analyze data, available analysis workflows, and interaction with MiSeq Control Software V4.
Sequencing Data Analysis: Introduction to Key Concepts
PastWebinar
Dec 22
Sequencing Data Analysis: Introduction to Key Concepts
Dec 22, 2022
This webinar is intended to introduce key data analysis and bioinformatics concepts used in analysis of Illumina sequencing data. This webinar is targeted for those that are new or intermediate to Illumina Next Generation Sequencing analysis, specifically biologists looking to understand data analysis.
Short and long RNAs in liquid biopsy: How to sequence them and what they tell us about cancer
PastWebinar
Jan 24
Short and long RNAs in liquid biopsy: How to sequence them and what they tell us about cancer
Jan 24, 2023
Speakers discuss methodologies for sequencing long or short RNAs from liquid biopsy samples, along with implications for cancer research.
A multi-species, low-cost, genome-wide genotyping platform to support molecular breeding in small grains
PastWebinar
Jan 26
A multi-species, low-cost, genome-wide genotyping platform to support molecular breeding in small grains
Jan 26, 2023
USDA agricultural genetic scientist Jason Fiedler will speak on the Infinium II array use cases.
NovaSeq X series: This is the genome era
PastWebinar
Feb 07
NovaSeq X series: This is the genome era
Feb 7, 2023
Hear how the NovaSeq X Series enables more powerful studies while offering maximum throughput and transformative economics, more sustainably than ever.
Advancements in whole-genome sequencing - AGBT Spotlight Talk
PastWebinar
Feb 08
Advancements in whole-genome sequencing
Feb 8, 2023
Learn how improvements in informatics are advancing whole-genome sequencing, and find out the latest on Illumina Complete Long Reads.
AGBT Workshop
PastWebinar
Feb 08
NovaSeq X and innovations across the Illumina portfolio
Feb 8, 2023
Hear about the latest on the Illumina portfolio. Also, learn about the Broad Institute's experiences with WGS data quality and performance from their early NovaSeq X runs.
NextSeq 1000 and 2000: Product updates and key applications
PastWebinar
Feb 09
NextSeq 1000 and 2000: Product updates and key applications
Feb 9, 2023
Learn about the latest in technology and consumables development on the NextSeq 1000 and 2000.
AGBT 2023: NovaSeq™X and Innovations Across the Illumina Portfolio
PastWebinar
Feb 16
AGBT 2023: NovaSeq™X and Innovations Across the Illumina Portfolio
Feb 16, 2023
Illumina invites you to join us and learn more about the exciting announcements and presentations from the 2023 Advances in Genome Biology and Technology (AGBT) General Meeting including the latest, Illumina Complete Long Reads, Human, NovaSeq™X, DRAGEN™ Onboard, and XLEAP-SBS™.
Metagenomics Part I: Introduction to Library Preparation and Sequencing
PastWebinar
Feb 28
Metagenomics Part I: Introduction to Library Preparation and Sequencing
Feb 28, 2023
Illumina Technical Support invites you to join us to discuss the end-to-end workflow for a Metagenomics sequencing project. This webinar is ideal for new and intermediate users of Illumina Next Generation Sequencing with an interest in metagenomics. We will discuss targeted metagenomics and shotgun metagenomics sequencing by including the following topics: An overview of metagenomics; Introduction to experimental approaches; Library preparation strategies and considerations; Sequencing options; Run performance evaluation; High-level overview of data analysis.
Workflow best practices: Exome Sequencing
PastWebinar
Feb 28
Workflow best practices: Exome Sequencing
Feb 28, 2023
Flawless execution of a library preparation is critical for getting good quality data. Listen to Inger Lomax from Illumina’s Technical Support Team talk about enrichment workflow best practices using Illumina DNA Prep with Exome 2.0 Plus Enrichment kit. During the webinar, Dr. Lomax will discuss topics such as What is the new Exome 2.0 Plus; Pre-enrichment input sample QC; Best practice of working with sample purification beads; Critical steps in post-enrichment steps; Enrichment statistics and what could they tell you about potential issues with your library prep protocol execution.
biomarkers
PastWebinar
Mar 02
Comprehensive Genomic Profiling in the Community Setting: Perspective from a Pathologist and an Oncologist
Mar 2, 2023
Dr. Carlo Bifulco and Dr. Rachel Sanborn provide insights into the benefits of in-house CGP testing at Providence Cancer Institute.
Lab worker with pipette
PastWebinar
Mar 17
Illumina Complete Long Reads
Mar 17, 2023
Highlights of research around the world using Illumina Complete Long Reads.
Lab worker with pipette
PastWebinar
Mar 17
[KR] - Illumina Complete Long Reads
Mar 17, 2023
Illumina Complete Long Reads - 복잡한 유전체에서 희귀 질환에 대한 통찰력을 얻어 보세요
Metagenomics Part 2: Introduction to Analysis
PastWebinar
Mar 21
Metagenomics Part 2: Introduction to Analysis
Mar 21, 2023
Illumina Technical Support invites you to join us in the part 2 of a 2-part Metagenomics Webinar series. Following Metagenomics Sequencing Part I, in this webinar, we will discuss Introduction to Data Analysis in Metagenomics. We assume a basic understanding of Illumina sequencing technology and knowledge of library prep workflow for Metagenomics. We will discuss the following topics: Overview of Targeted Metagenomics and Shotgun Metagenomics; Options for Metagenomics Data Analysis: 16s Metagenomics App and DRAGEN metagenomics Pipeline on BaseSpace Sequence Hub; and Overview of DRAGEN RNA Pathogen Detection App on BaseSpace.
신제품 업데이트:  Illumina Complete Long Reads
PastWebinar
Apr 27
신제품 업데이트: Illumina Complete Long Reads
Apr 27, 2023
Illumina Complete Long Reads의 효율적이고 확장 가능한 워크플로우와 얼리 액세스 고객분들의 실제 사용 경험을 확인해 보실 수 있습니다.
Single cell multiomics: Beyond RNA-Seq
PastWebinar
Apr 28
Single cell multiomics: Beyond RNA-Seq
Apr 28, 2023
Dr. Michael Kelly of the Frederick National Laboratory discusses projects that he supports utilizing single cell and spatial technologies across both basic science and more translational research questions.
MiSeq: Run Quality and Best Practices
PastWebinar
May 03
MiSeq: Run Quality and Best Practices
May 3, 2023
Technical Support invites users to join us for a discussion of the MiSeq system. The MiSeq System offers integrated cluster generation, amplification, sequencing, and data analysis into a single instrument. This webinar will go through troubleshooting considerations at each of these steps and is targeted toward new and intermediate users with a basic understanding of the Illumina sequencing workflow and the Sequence Analysis Viewer (SAV) software. We will cover the following topics: run setup and start best practices, assessment of runs in progress using SAV, and tips and best practices.
Accelerating precision medicine with low-cost whole-genome sequencing
PastWebinar
May 11
Accelerating precision medicine with low-cost whole-genome sequencing
May 11, 2023
This expert roundtable discusses the range of opportunities that widely accessible whole-genome sequencing presents for precision medicine.
Illumina Connected Analytics: Streamlined sequencer integration and automation of secondary analysis workflows
PastWebinar
May 23
Illumina Connected Analytics: Streamlined sequencer integration and automation of secondary analysis workflows
May 23, 2023
Illumina Connected Analytics - A secure genomic data platform to operationalize informatics and drive scientific insights. Illumina Connected Analytics brings forth exciting new advancements – including streamlined data transfer from Illumina sequencing instruments, automation of BCL Convert and DRAGEN™ secondary analysis pipelines, and the release of TruSight™ Oncology 500 (TSO500) v2.1 pipelines. Key learning objectives includes: Understand the workflow between BaseSpace™ Sequence Hub and Connected Analytics for flexible run setup options; Level of support for instrument integration for each Illumina sequencer; and Details around the availability of TSO500 v2.1 pipelines.
Advancing detection and monitoring of drug-resistance tuberculosis with Next-Generation Sequencing
PastWebinar
May 30
Advancing detection and monitoring of drug-resistance tuberculosis with Next-Generation Sequencing
May 30, 2023
The Genoscreen Deeplex Myc-TB next generation sequencing (NGS) assay detects more than 100 mycobacterium species and provides an extensive drug resistance profile for 15 antibiotics commonly used for TB. Results are available in less than 48 hours directly from a sputum sample or cultured isolate. TB identification with drug resistance in an actionable timeframe is a leap forward in managing and monitoring tuberculosis. At the end of this webinar, attendees will be able to: - Understand the current tuberculosis landscape and global impact of drug resistance on TB management - Describe how next-generation sequencing is used to identify and monitor TB drug resistance - Explain how the Deeplex Myc-TB assay fits into a laboratory workflow.
Advancing detection and monitoring of drug-resistance tuberculosis with next-generation sequencing (NGS)
PastWebinar
May 30
Advancing detection and monitoring of drug-resistance tuberculosis with next-generation sequencing (NGS)
May 30, 2023
Learn how next-generation sequencing (NGS) is used to identify, detect, and monitor TB drug resistance using the Deeplex Myc-TB assay.
NextSeq 2000
PastWebinar
Jun 13
NextSeq 1000/2000: Longer reads and extended informatics
Jun 13, 2023
During this webinar and Q&A session, we discuss key NextSeq 1000 and 2000 product updates and features of the onboard DRAGEN Bio-IT platform.
Empowering Infectious Disease Surveillance: Territory Pathology's Journey from NGS Novices to Pioneers in the Field
PastWebinar
Jun 13
Empowering Infectious Disease Surveillance: Territory Pathology's Journey from NGS Novices to Pioneers in the Field
Jun 13, 2023
The Northern Territory of Australia, retains a unique and substantially diverse range of infectious diseases, thus highlighting the necessity of offering rapid, reliable and cost-effective diagnostic and epidemiological surveillance methods. Due to the immense global pressure for epidemiological surveillance of the SARS-CoV-2 virus, rural and remote laboratories such as Territory Pathology were provided with the opportunity to establish local NGS capacity.
Sequencing Data Analysis: Introduction to Key Concepts
PastWebinar
Jun 16
Sequencing Data Analysis: Introduction to Key Concepts
Jun 16, 2023
The next-generation sequencing (NGS) generates large volumes of data which can be converted into meaningful information via data analysis pipelines. This webinar is intended to introduce key data analysis and bioinformatics concepts used in analysis of Illumina sequencing data. The content of webinar is suitable for researchers who are new or intermediate to NGS data analysis and interested in Illumina analysis solutions.
Adapting to New Threats/Rapid Pivot
PastWebinar
Jul 11
Adapting to New Threats/Rapid Pivot
Jul 11, 2023
From COVID-19 pandemic response to One Health Genomic Surveillance
DRAGEN™ 4.2: Enhanced machine learning, new targeted callers, and more
PastWebinar
Jul 18
DRAGEN™ 4.2: Enhanced machine learning, new targeted callers, and more
Jul 18, 2023
Learn about the features and benefits of DRAGEN v4.2. In this webinar, we dive into how DRAGEN leverages its award-winning accuracy and comprehensive, efficient workflows to help unlock the full potential of genomics.
Unlocking the Power of Microbiome Research - Best Practices and Key Considerations
PastWebinar
Jul 26
Unlocking the Power of Microbiome Research - Best Practices and Key Considerations
Jul 26, 2023
In conjunction with our recently published Microbiome Considerations series, where we share our best advice and essential considerations for getting high-quality metagenomics data for your microbiome study – including best practices for sample collection, sequencing techniques, and data analysis through advanced bioinformatics. This webinar highlights these considerations and leverages as a platform to ask our expert panel questions on microbiome research. The three key things you'll learn in this webinar are: To share best practices for sample collection, sequencing techniques, and data analysis through advanced bioinformatics. To provide insights into how to maximize accuracy and reliability of microbiome data. To communicate valuable experiences that can be applied to your own research
Illumina DRAGEN™ 4.2: Enhanced machine learning, new targeted callers, and more
PastWebinar
Jul 27
Illumina DRAGEN™ 4.2: Enhanced machine learning, new targeted callers, and more
Jul 27, 2023
DRAGEN v4.2 is here with new features including DRAGEN’s most accurate SNV and SV calling powered by machine learning enhancements, new targeted callers for carrier screening and LPA, and support for Telomere-to-Telomere (T2T) CHM13 reference, and more, furthering DRAGEN’s incredible accuracy improvements. DRAGEN v4.2 expands the breadth of pipelines with the new Explify Respiratory Pathogen Panel (RPIP), Urinary Pathogen Panel (UPIP) pipeline, and updates to metagenomics pipelines. Hear more about the new accuracy gains and more in the upcoming technical webinar on DRAGEN 4.2.
Advancing Antimicrobial Resistance Surveillance with Illumina Genomics Solutions
PastWebinar
Aug 01
Advancing Antimicrobial Resistance Surveillance with Illumina Genomics Solutions
Aug 1, 2023
Antimicrobial resistance (AMR) is a significant global health crisis, affecting human, animal, and environmental health. Addressing this urgent issue requires a coordinated "One Health" approach and innovative solutions, such as genomics.
CZ ID - A Free, Open Source, Cloud-based Tool for Metagenomic Pathogen Detection and Monitoring
PastWebinar
Aug 22
CZ ID - A Free, Open Source, Cloud-based Tool for Metagenomic Pathogen Detection and Monitoring
Aug 22, 2023
Metagenomic next-generation sequencing (mNGS) has enabled the rapid, unbiased detection and identification of microbes without pathogen-specific reagents, culturing, or a priori knowledge of the microbial landscape. However, mNGS data analysis requires a series of computationally intensive processing steps, bioinformatics expertise, and access to local server-class hardware resources, which presents an obstacle for many research laboratories, especially those in resource-limited environments.
Accelerate target discovery with Illumina’s Correlation Engine
PastWebinar
Aug 23
Accelerate target discovery with Illumina’s Correlation Engine
Aug 23, 2023
Illumina’s Correlation Engine is an interactive omics knowledgebaseQQ that puts private data in biological context with highly curated public data in a comprehensive and easy to use platform. Explore how you can leverage Correlation Engine to accelerate your multiomics research from drug discovery, through target discovery and more.
Single-cell RNA sequencing across multiple sites
PastWebinar
Aug 24
Single-cell RNA sequencing across multiple sites
Aug 24, 2023
Advances in technology are enabling single-cell RNA sequencing experiments to leverage cell preservation so that samples can be collected from multiple sites and still sequenced in a single Integrated workflow.
Unlock the next wave of genomic discovery with NovaSeq X
PastWebinar
Oct 04
Unlock the next wave of genomic discovery with NovaSeq X
Oct 4, 2023
In this webinar, we highlight key features of the NovaSeq X series including technology innovations, product updates, and features of the on-board DRAGEN Bio-IT secondary analysis.
Introduction to Sequencing by Synthesis
PastWebinar
Oct 04
Introduction to Sequencing by Synthesis
Oct 4, 2023
This webinar offers a concise overview of the sequencing by synthesis (SBS) process, covering the steps from library preparation, cluster generation, sequencing to data analysis. Participants will gain insights into the DNA synthesis using DNA polymerases and dNTPs for sequencing. Additionally, the webinar will introduce the Illumina chemistry channels and their significance in SBS. It is designed for individuals at both beginner and intermediate levels who are interested in Illumina's sequencing technologies.
Insights into leveraging new capabilities and applications on the NovaSeq X
PastWebinar
Nov 03
Insights into leveraging new capabilities and applications on the NovaSeq X
Nov 3, 2023
Eric Chow discusses how to leverage the NovaSeq X platform's capabilities to drive applications and optimize workflows in the lab.
Illumina innovations and products to unlock the next wave of genomic discovery
PastWebinar
Nov 03
Illumina innovations and products to unlock the next wave of genomic discovery
Nov 3, 2023
Gary Schroth highlights advancements, impacts, and the exciting potential of how Illumina technology is unlocking discoveries and enabling insights in the field of genomics.
Advancing epigenetic breakthroughs with the Illumina NextSeq 1000/2000
PastWebinar
Nov 03
Advancing epigenetic breakthroughs with the Illumina NextSeq 1000/2000
Nov 3, 2023
Learn about the latest advancements in sequencing technology and their transformative impact on human disease research.
Highlighting the importance of diversity in cohorts and careers: A fireside chat
PastWebinar
Nov 04
Highlighting the importance of diversity in cohorts and careers: A fireside chat
Nov 4, 2023
Dr. Catherine Tcheandjieu speaks with Melissa Dempsey about the impact and importance that diversity in cohorts and in the genomics workforce plays in the implementation and utilization of genomics.
Unlock genomic insights for rare & hereditary disease with Emedgene
PastWebinar
Nov 09
Unlock genomic insights for rare & hereditary disease with Emedgene
Nov 9, 2023
With the adoption of genomic tests growing, streamlining data curation and interpretation is more important than ever. Emedgene can help you unlock genomic insights and confidently scale your tertiary analysis workflows for rare disease genomics and other germline research applications with explainable AI (XAI) and workflow automation. Discover how this tertiary analysis software can speed up your germline analysis and provide you with multiple benefits today.
TruSight Oncology 500 and TruSight Oncology 500 HRD: Introduction & Overview
PastWebinar
Nov 15
TruSight Oncology 500 and TruSight Oncology 500 HRD: Introduction & Overview
Nov 15, 2023
TruSight Oncology 500 is a next-generation sequencing tumor profiling assay that analyzes 523 genes for cancer-related biomarkers with FFPE samples. The assay supports the identification of DNA and RNA variants implicated in various tumor types, including measuring key immunotherapy biomarkers such as tumor mutation burden (TMB) and microsatellite instability (MSI). This webinar focuses on introducing TruSight Oncology 500/TruSight Oncology 500 HRD library preparation and is targeted at new users of the workflow. We cover the following topics: how to successfully prepare and sequence TruSight Oncology 500 libraries and changes in HRD workflow.
Achieving high sensitivity and concordance from CGP from “liquid biopsy” specimens
PastWebinar
Nov 15
Achieving high sensitivity and concordance from CGP from “liquid biopsy” specimens
Nov 15, 2023
In this workshop, we will discuss important considerations when establishing a ctDNA CGP assay to ensure high sensitivity and concordance; share practical implementation challenges and proposed solutions experienced in a community-based, Integrated Network Cancer Program. 
Implementing CGP + HRD testing in-house in a large US Healthcare System
PastWebinar
Nov 15
Implementing CGP + HRD testing in-house in a large US Healthcare System
Nov 15, 2023
Homologous recombination repair deficiency (HRD) is associated with response to poly-ADP-ribose polymerase inhibition (PARPi) therapy in advanced ovarian cancer.
Sequencing: Optimizing Cluster Density
PastWebinar
Nov 22
Sequencing: Optimizing Cluster Density
Nov 22, 2023
Monitoring the behavior of cluster density is crucial to understanding its overall impact on the quality of a sequencing run. Here we will learn more about cluster density and factors which influence its yield. We will also discuss tips and tricks for achieving optimal cluster density as well as how to track and correlate it to library loading concentration. The webinar will be targeted for both new and intermediate users of Illumina’s sequencing technologies.
BaseSpace™ Sequence Hub - Introduction and Analysis Overview
PastWebinar
Jan 24
BaseSpace™ Sequence Hub - Introduction and Analysis Overview
Jan 24, 2024
In this webinar, we'll talk about how BaseSpace Sequence Hub may help increase organizational productivity by giving users easy access to a variety of genomic analysis tools and computing resources without the capital expenditure of an in-house infrastructure. We will cover the following topics: How to navigate the BaseSpace dashboard, BaseSpace functionally, How to upload/view data in BaseSpace, discussion of major analysis workflows, general overview of how to analyze data on BaseSpace.
Scaling a clinical sequencing workflow for rare disease research
PastWebinar
Feb 06
Scaling a clinical sequencing workflow for rare disease research
Feb 6, 2024
Learn how Illumina sequencing platforms are accelerating rare disease research in hospitals.
Illumina sequencing innovations powered by XLEAP-SBS chemistry
PastWebinar
Feb 07
Illumina sequencing innovations powered by XLEAP-SBS chemistry
Feb 7, 2024
Learn about the latest Illumina sequencing updates and innovations on the NovaSeq X and NextSeq 1000/2000 platforms.
Highly accurate, flexible targeted long reads to resolve challenging regions of the genome
PastWebinar
Feb 07
Highly accurate, flexible targeted long reads to resolve challenging regions of the genome
Feb 7, 2024
Learn about the latest Illumina sequencing updates and innovations on the NovaSeq X and NextSeq 1000/2000 platforms.
Illumina sequencing innovations powered by XLEAP-SBS chemistry and targeted long reads
PastWebinar
Feb 07
Illumina sequencing innovations powered by XLEAP-SBS chemistry and targeted long reads
Feb 7, 2024
Learn about the latest Illumina sequencing updates and innovations on the NovaSeq X and NextSeq 1000/2000 platforms.
Panel Discussion on Getting Started with NGS
PastWebinar
Feb 13
Panel Discussion on Getting Started with NGS
Feb 13, 2024
How to get started with NGS Panel Discussion. Join us for our panel discussion with 4 NGS experts.
AGBT 2024: Illumina Sequencing Innovations Powered by XLEAP-SBS™ Chemistry
PastWebinar
Feb 15
AGBT 2024: Illumina Sequencing Innovations Powered by XLEAP-SBS™ Chemistry
Feb 15, 2024
Join Dr. Anthony Beckhouse, Senior Manager, Regional Product Marketing Systems Lead, Illumina, presenting all the exciting Illumina announcements from the 2024 Advances in Genome Biology and Technology (AGBT) General Meeting, including the latest Illumina sequencing innovations powered by XLEAP-SBS™ chemistry.
Infinium Methylation – Introduction to Analysis
PastWebinar
Mar 07
Infinium Methylation – Introduction to Analysis
Mar 7, 2024
The Infinium MethylationEPIC v2.0 BeadChip Kit is a genome-wide methylation screening tool that targets the identification of over 935,000 CpGs per sample with single-nucleotide precision across FFPE and fresh sample types. The Infinium methylation technology not only fueled groundbreaking discoveries but also paved the way for the practical application of methylation-based biomarkers in diverse fields such as cancer research, genetic diseases, aging, and molecular epidemiology. This webinar provides a comprehensive overview of the Infinium methylation platform focusing MethylationEPIC v2.0 data analysis using GenomeStudio Methylation Module.
Preparing for a genome world: AI and informatics automation at the core
PastWebinar
Mar 14
Preparing for a genome world: AI and informatics automation at the core
Mar 14, 2024
Learn how Baylor Genetics leverages their AI and informatics automation workflow catalyze their operability for meeting a genome world.
Chromosomal Microarray: A journey in clinical cytogenetics
PastWebinar
Mar 20
Chromosomal Microarray: A journey in clinical cytogenetics
Mar 20, 2024
Chromosomal microarray technology was introduced into diagnostic pathology services as the first-tier investigation of constitutional anomalies from 2010. It is now considered the gold standard mode of cytogenetic testing, applied to investigate valid clinical indications in post-natal, pre-natal, neoplastic disease and products of conception. Nicole will share her experience and the fundamental steps to consider when launching a molecular cytogenetic service or changing between microarray platforms.
TruSight Oncology 500 Portfolio - 조직과 액체생검에서 포괄적 유전체 프로파일링을 위한 TSO500 포트폴리오
PastWebinar
Mar 28
TruSight Oncology 500 Portfolio - 조직과 액체생검에서 포괄적 유전체 프로파일링을 위한 TSO500 포트폴리오
Mar 28, 2024
TruSight Oncology 500 family is a next-generation sequencing tumor profiling assay that analyzes 523 genes for cancer-related biomarkers with FFPE samples. The assay supports the identification of DNA and RNA variants implicated in various tumor types, including measuring key immunotherapy biomarkers such as tumor mutation burden (TMB) and microsatellite instability (MSI). This webinar provides an overview of TruSight Oncology 500 portfolio including analysis and is targeted at new users of the workflow. We will also introduce TSO500 ctDNA v2 and illumina cfDNA Enrichment for liquid biopsy. Please take note that this webinar is conducted in Korean language.
Side view of scientist inserting a XLEAP SBS P4 flow cell into reagent cartridge
PastWebinar
Apr 15
The Making of XLEAP-SBS Chemistry
Apr 15, 2024
In this webinar Pietro Gatti, Associate Director & Future Tech Strategy Lead is joined by the Illumina science team to showcase the research and development that went into building the new XLEAP-SBS Chemistry.
Illumina artificial intelligence: PrimateAI-3D and SpliceAI for precision medicine and drug discovery
PastWebinar
Apr 16
Illumina artificial intelligence: PrimateAI-3D and SpliceAI for precision medicine and drug discovery
Apr 16, 2024
Dr. Kyle Farh reviews the data illustrating the impact that these two algorithms have on our understanding of variants of unknown significance (VUS) and the non-coding region of the genome.
Leverage genomic AI to deliver a more accurate and comprehensive genome
PastWebinar
Apr 17
Leverage genomic AI to deliver a more accurate and comprehensive genome
Apr 17, 2024
Discover more about Illumina’s proprietary AI algorithms and their impact, from DRAGEN Machine Learning, Emedgene Explainable AI (XAI), and Illumina Connected Annotations PrimateAI-3D and SpliceAI.
Introduction to the New XLEAP-SBS technology on NextSeq 1000/2000 Systems, Best Practices and Run Quality Management [Korean]
PastWebinar
Apr 18
Introduction to the New XLEAP-SBS technology on NextSeq 1000/2000 Systems, Best Practices and Run Quality Management [Korean]
Apr 18, 2024
이 웨비나는 NextSeq 1000 및 2000 시스템의 향상된 스펙과 기능을 소개하며, 실행 성능을 극대화하기 위한 모범 사례와 해결책을 제공합니다. 또한, Illumina의 표준 SBS chemistry를 기반으로 한 최신 기술인 XLEAP-SBS chemistry에 대해서도 다룰 예정입니다. 이 기술은 시퀀싱의 속도와 품질을 향상시키는 데 중점을 둔 강력한 방법입니다. XLEAP-SBS chemistry를 통해 구현된 Illumina 시퀀싱의 최신 데이터와 혁신기술을 소개드릴 예정입니다. Please take note that this webinar is conducted in Korean language.
Advancements for your core like never before
PastWebinar
Apr 23
Advancements for your core like never before
Apr 23, 2024
Illumina Chief Technology Officer, Steve Barnard, provides a detailed overview of our latest innovations and how Illumina is working to provide your labs with the best and most efficient technology.
Discover what's possible with XLEAP-SBS chemistry
PastWebinar
Apr 23
Discover what's possible with XLEAP-SBS chemistry
Apr 23, 2024
Listen to Zymo sequencing researcher, Ethan Thai, discuss the premium-quality data and achievements they have made by using XLEAP-SBS chemistry on their NextSeq 2000.
Let X equal…
PastWebinar
Apr 23
Let X equal…
Apr 23, 2024
Listen to Oklahoma Medical Research Foundation’s core director, Graham Wiley, speak to all of the ways the NovaSeq X has made his lab’s research more efficient and cost saving.
Scientist analyzing data behind computer screen
PastWebinar
Apr 23
The complexities of spatial multiomics unraveled
Apr 23, 2024
Explore in situ gene and protein expression in tonsil tissues to gather meaningful and applicable results
NextSeq™ 1000 and 2000 Run Quality and Best Practices
PastWebinar
Apr 29
NextSeq™ 1000 and 2000 Run Quality and Best Practices
Apr 29, 2024
This support webinar discusses the NextSeq 1000 and 2000 sequencers and reagents, including the introduction of XLEAP-SBS™ chemistry, pre-run considerations, run setup, run start best practices, run metrics review, and maintenance. This webinar is for anyone who wants to learn more about the NextSeq 1000/2000 Run Quality and Best Practices.
MiSeq™ Best Practices and Troubleshooting
PastWebinar
May 23
MiSeq™ Best Practices and Troubleshooting
May 23, 2024
Miseq 시스템은 클러스터 생성에서부터 증폭, 시퀀싱, 데이터 분석에 이르기까지 전 과정을 원스톱으로 제공하는 벤치탑 시퀀서입니다. 이로 인해 다양한 시퀀싱 어플리케이션에 적합하며, 사용자 친화적인 엔드 투 엔드 워크플로우로 인해 널리 선호되고 있습니다.
Oncology Small Panel: Introduction
PastWebinar
May 28
Oncology Small Panel: Introduction
May 28, 2024
A walk through the AmpliSeq for Illumina which offers a suite of AmpliSeq chemistry products that are compatible with Illumina next-generation sequencing platforms.
Single cell bioinformatics for researchers
PastWebinar
May 30
Single cell bioinformatics for researchers
May 30, 2024
Understanding the bioinformatics of single cell analysis without being a bioinformatician
DRAGEN™ 4.3: Next-generation multigenome, new specialized callers for difficult regions of the genome
PastWebinar
Jun 21
DRAGEN™ 4.3: Next-generation multigenome, new specialized callers for difficult regions of the genome
Jun 21, 2024
DRAGEN™ v4.3 is here with new features that enhance the coverage of the genome including a next-generation multigenome (graph) reference that can now incorporate hundreds of high-quality assemblies such as those built by the Human Pangenome Reference Consortium (HPRC).
Clinical utility of whole-genome DNA methylation profiling as a primary molecular diagnostic assay for central nervous system tumors
PastWebinar
Jun 26
Clinical utility of whole-genome DNA methylation profiling as a primary molecular diagnostic assay for central nervous system tumors
Jun 26, 2024
Sharing various clinical cases, Dr. Snuderl will show that DNA methylation is currently the only pan CNS tumor assay that incorporates detection of all other biomarkers, decreasing the cost, turnaround time and tissue wastage associated with sequential molecular testing and diagnostic errors.
Illumina DRAGEN v4.3: Comprehensive coverage with leading edge innovations
PastWebinar
Jun 26
Illumina DRAGEN v4.3: Comprehensive coverage with leading edge innovations
Jun 26, 2024
Learn about the new features of DRAGEN v4.3 in this technical webinar.
Applications of Epigenetic Aging Clocks and Methylation Risk Scores using Whole Genome Methylation Profiling
PastWebinar
Jul 24
Applications of Epigenetic Aging Clocks and Methylation Risk Scores using Whole Genome Methylation Profiling
Jul 24, 2024
Analysis surrounding DNA methylation (DNAm) data is growing at an exponential pace. For instance, the number of Epigenome-Wide Association Studies (EWAS) per year has tripled since 2016. In addition to having a much higher focus from research and biotech communities, data is also becoming more available as more researchers and biobanks commit to doing analysis on the low cost but high yield DNA methylation array platforms. However, methods to quickly analyze this data are still limited and not widely available.
Illumina Metagenomics Application & Analysis
PastWebinar
Jul 25
Illumina Metagenomics Application & Analysis
Jul 25, 2024
메타지노믹스는 배양 과정을 거치지 않고 시퀀싱을 통해 미생물 군집의 Diversity(다양성)와 Abundance(풍부도) 및 기능유전체를 연구하는 분야입니다. 이번 웨비나에서는 장내 미생물뿐만 아니라 토양, 해양 등 다양한 환경 샘플을 대상으로 메타지노믹스를 연구할 수 있는 일루미나의 16S & Shotgun Metagenomics Applications를 소개합니다. 또한, 16S Metagenomics와 Shotgun Metagenomics 실험 차이점을 살펴보고, 라이브러리 준비 과정부터 플랫폼별 시퀀싱 옵션 및 고려사항까지 다룰 예정입니다. 마지막으로 데이터 분석을 위한 일루미나의 BaseSpace App을 소개하고, 다양한 분석 어플리케이션을 통해 분석 역량을 강화하는 방법을 안내해드립니다.
Illumina® Sequencing: How to Plan Your First Sequencing Project
PastWebinar
Jul 31
Illumina® Sequencing: How to Plan Your First Sequencing Project
Jul 31, 2024
Embarking on your first sequencing project can be both exciting and daunting. Join us for a comprehensive webinar where we will guide you through every step of the process, from initial considerations to final analysis. Whether you're new to genomics or seeking to optimize your workflow, this session is designed to equip you with the knowledge and resources needed for success.
Sequencing Data Analysis Fundamental  – Part 1 [Korean]
PastWebinar
Aug 22
Sequencing Data Analysis Fundamental – Part 1 [Korean]
Aug 22, 2024
시퀀싱 기술이 발전함에 따라 더 빠르고 더 많은 데이터를 생산할 수 있게 되었으며 그 어느 때보다 유전체 데이터가 풍부한 시대에 살아가고 있습니다. 이번 웨비나는 Illumina 시퀀싱 데이터 분석에 사용되는 생물정보학의 주요 개념들에 대해 살펴보고 실험 설계 시 고려해야할 사항들에 대해 소개할 예정입니다. 또한 플랫폼 별로 적용 가능한 어플리케이션들을 살펴보고 데이터 분석 경험을 개선하는 데 사용될 수 있는 다양한 분석 솔루션을 소개할 예정입니다.
Sequencing Data Analysis: Introduction to Key Concepts
PastWebinar
Aug 27
Sequencing Data Analysis: Introduction to Key Concepts
Aug 27, 2024
This webinar is intended to introduce key data analysis and bioinformatics concepts used in analysis of Illumina sequencing data. This webinar is targeted for those that are new or intermediate to Illumina Next-Generation Sequencing analysis, specifically biologists looking to understand data analysis.
Planning and preparing your first NGS Project
PastWebinar
Sep 05
Planning and preparing your first NGS Project
Sep 5, 2024
Using next generation sequencing (NGS), researchers maximize the discoveries they can make per sample by identifying variants and expression patterns across thousands of target regions.
GenomeStudio™: Advanced Analysis Tools
PastWebinar
Sep 25
GenomeStudio™: Advanced Analysis Tools
Sep 25, 2024
This webinar will demonstrate the use of various tools and techniques within the GenomeStudio Genotyping and Methylation modules, including heritability and reproducibility analysis, and GenderEst gender estimation tool. Additionally, we will discuss how to use cluster editing tools and touch on important image viewing functionalities.
How to streamline bulk RNA-Seq analysis
PastWebinar
Sep 26
How to streamline bulk RNA-Seq analysis
Sep 26, 2024
How to perform each analysis step using simple point-and-click actions that you can replicate in your own analysis.
webinar image
PastWebinar
Oct 09
Innovations to unlock the next wave of genomic discovery
Oct 9, 2024
Get exciting sequencing technology updates.
NovaSeq X Series: One flow cell, multiple omes
PastWebinar
Oct 09
NovaSeq X Series: One flow cell, multiple omes
Oct 9, 2024
Learn how the innovations of NovaSeq X are making multiomics a reality. We will highlight data from multi-project runs, massive single-cell and CRISPR applications, and developing a protocol for liquid biopsy.
In-house Hereditary Cancer Testing
PastWebinar
Oct 16
In-house Hereditary Cancer Testing
Oct 16, 2024
Hear experts discuss the evolution of guideline-based testing for hereditary prostate cancer from a historical to present clinical perspective.
How to explore Fluent single cell data
PastWebinar
Oct 17
How to explore Fluent single cell data
Oct 17, 2024
Introduction to the basic tertiary scRNA-Seq analyses steps.
For All You Seq: Benchtop sequencing applications
PastWebinar
Oct 23
For All You Seq: Benchtop sequencing applications
Oct 23, 2024
Discover how XLEAP-SBS chemistry is transforming sequencing workflows on both the MiSeq i100 and NextSeq 1000/2000.
Pillar Biosciences’ oncoReveal CDx Pan-Cancer Solid Tumor IVD
PastWebinar
Oct 23
Pillar Biosciences’ oncoReveal CDx Pan-Cancer Solid Tumor IVD
Oct 23, 2024
Access to rapid, reproducible and accurate NGS kitted assays are important as many laboratories navigate the FDA/LDT Final Rule and are required to provide faster NGS results to treating clinicians.
Sequencing Data Analysis Part 2 (Korean): Comprehensive DNA pipeline with BaseSpace Sequence Hub™ and Emedgene™.
PastWebinar
Oct 24
Sequencing Data Analysis Part 2 (Korean): Comprehensive DNA pipeline with BaseSpace Sequence Hub™ and Emedgene™.
Oct 24, 2024
This webinar provides an overview of DRAGEN DNA pipeline used in analysis of Illumina sequencing data. We also introduce DRAGEN Germline application on BaseSpace Sequence Hub™ that can be used to improve your data analysis experience. Whether you are new or would just like a refresher, this webinar will give you a robust overview of DRAGEN DNA pipeline and Germline analysis with Illumina Software.
Your Vision Our Workflow - Illumina’s solution for clinical research in rare and inherited disease
PastWebinar
Nov 06
Your Vision Our Workflow - Illumina’s solution for clinical research in rare and inherited disease
Nov 6, 2024
In this webinar you will hear from two speakers: Anthony Beckhouse on the benefits and flexibility of the NextSeq 1K/2k, and Michael Fietz on the accuracy and speed of our secondary analysis solution DRAGEN, as well as how our tertiary analysis solution Emedgene can help address bottlenecks of analysis and reporting for rare and inherited disease research. With Illumina’s exome or genome sequencing as a backbone, and the ability to do virtual panels with our tertiary solution - Emedgene. Laboratories can now create comprehensive assays to enable the latest genomic discoveries.
Your Vision Our Workflow - Illumina’s solution for clinical research in rare and inherited disease
PastWebinar
Nov 06
Your Vision Our Workflow - Illumina’s solution for clinical research in rare and inherited disease
Nov 6, 2024
In this webinar you will hear from two speakers: Anthony Beckhouse on the benefits and flexibility of the NextSeq 1K/2k, and Michael Fietz on the accuracy and speed of our secondary analysis solution DRAGEN, as well as how our tertiary analysis solution Emedgene can help address bottlenecks of analysis and reporting for rare and inherited disease research. With Illumina’s exome or genome sequencing as a backbone, and the ability to do virtual panels with our tertiary solution - Emedgene. Laboratories can now create comprehensive assays to enable the latest genomic discoveries.
Illumina Innovation Roadmap
PastWebinar
Nov 06
Illumina Innovation Roadmap
Nov 6, 2024
Hear from Steve Barnard about the latest Illumina innovations. Niall Lennon, PhD from the Broad Institute of MIT joins Steve to provide insights into new Illumina technology.
 Evaluation of circulating protein biomarkers for cancer detection using Illumina Protein Prep platform
PastWebinar
Nov 07
Evaluation of circulating protein biomarkers for cancer detection using Illumina Protein Prep platform
Nov 7, 2024
Krishna Morampudi provides an overview of the Illumina Protein Prep product and workflow. Dr. Kamel Lahouel of TGen presents a new pilot study using the Illumina Protein Prep assay.
Unlocking precision: The power of PIPseq V in scRNA-Seq
PastWebinar
Nov 07
Unlocking precision: The power of PIPseq V in scRNA-Seq
Nov 7, 2024
In this talk , we explore how PIPseq V enables researchers to delve deeper into the complexities of the genome, with a scalable, accessible solution and showcase the developing possibilities of single cell research.
DRAGEN™ Command line for Beginners
PastWebinar
Nov 20
DRAGEN™ Command line for Beginners
Nov 20, 2024
This webinar is designed to introduce beginners and non-bioinformaticians to the DRAGEN command line interface. DRAGEN is a powerful bioinformatics tool for secondary analysis of Next-Generation Sequencing (NGS) data. By understanding the command line, you can gain more flexibility and control over your analyses.
Challenges and practice gaps affecting implementation of oncology precision medicine
PastWebinar
Nov 20
Challenges and practice gaps affecting implementation of oncology precision medicine
Nov 20, 2024
Explore real-world gaps in biomarker testing and precision medicine. Gain expert insights on improving coordination for better outcomes. Recorded at AMP, November 2024.
Clinical scenarios demonstrating value of NGS for oncology biomarker testing of tissue and liquid specimens
PastWebinar
Nov 20
Clinical scenarios demonstrating value of NGS for oncology biomarker testing of tissue and liquid specimens
Nov 20, 2024
Gain expert insights on optimizing NGS for biomarker testing. Explore key clinical factors shaping specimen selection and sequencing success. Recorded at AMP, November 2024.
Practical considerations for integrating enterprise-wide pharmacogenomics (PGx)
PastWebinar
Nov 20
Practical considerations for integrating enterprise-wide pharmacogenomics (PGx)
Nov 20, 2024
Discover Atrium Health’s enterprise-wide PGx model. Learn strategies to overcome adoption barriers and drive precision medicine integration. Recorded at AMP, November 2024.
From genotypes to impact - using genetic information to breed better, more sustainable animals and plants
PastWebinar
Nov 25
From genotypes to impact - using genetic information to breed better, more sustainable animals and plants
Nov 25, 2024
Join us for an insightful webinar on cutting-edge genetic improvement programs. Bruno Santos, a Partner and Consultant at AbacusBio, will guide you through the latest advancements in genetic and genomic evaluation, selection index creation, and trait prioritization.
Illumina innovation roadmap
PastWebinar
Dec 06
Illumina innovation roadmap
Dec 6, 2024
Learn about the new innovative technology offerings from the Illumina product pipeline and introduce our newest system — the MiSeq i100 Series.
Meet the MiSeq i100 Series
PastWebinar
Dec 06
Meet the MiSeq i100 Series
Dec 6, 2024
Introducing our newest system: the MiSeq i100 Series. We walk through system specs and review key applications and methods.
Leverage new multiomics assays to go beyond today's genome
PastWebinar
Dec 06
Leverage new multiomics assays to go beyond today's genome
Dec 6, 2024
Learn how you can leverage new multiomics assays to go beyond today’s genome.
Noninvasive Prenatal Testing (NIPT): Understanding the Basics
PastWebinar
Jan 15
Noninvasive Prenatal Testing (NIPT): Understanding the Basics
Jan 15, 2025
Noninvasive Prenatal Testing (NIPT) is a screening test based on the analysis of cell-free DNA from maternal blood. Through a simple maternal blood draw, NIPT can noninvasively screen for fetal chromosomal aneuploidies as early as the 10th week of pregnancy. Genome-wide screening offers insights into partial duplications and deletions across all autosomes, as well as the aneuploidy status of all chromosomes. This webinar will cover the fundamentals of NIPT, including the underlying technology and key technical aspects of the test.
Noninvasive Prenatal Testing (NIPT): Understanding the Basics
PastWebinar
Jan 15
Noninvasive Prenatal Testing (NIPT): Understanding the Basics
Jan 15, 2025
Noninvasive Prenatal Testing (NIPT) is a screening test based on the analysis of cell-free DNA from maternal blood. Through a simple maternal blood draw, NIPT can noninvasively screen for fetal chromosomal aneuploidies as early as the 10th week of pregnancy. Genome-wide screening offers insights into partial duplications and deletions across all autosomes, as well as the aneuploidy status of all chromosomes. This webinar will cover the fundamentals of NIPT, including the underlying technology and key technical aspects of the test.
Depiction of DNA
PastWebinar
Feb 23
2025 Advances in Genome Biology and Technology (AGBT) Meeting
Feb 23, 2025
Join Illumina at AGBT as we unveil the next breakthrough in next-generation sequencing and multiomics.
Illumina’s Integrated Workflow for Rare and Undiagnosed Genetic Disease Research
Webinar
Feb 26
Illumina’s Integrated Workflow for Rare and Undiagnosed Genetic Disease Research
Feb 26, 2025
Individuals suspected of having a rare disease often face a long search for an answer. With up to 80% of rare diseases being genetic or having a genetic subtype, it is imperative to interrogate the genome to find answers and shorten the diagnostic odyssey. This webinar provides an overview of the integrated workflow provided by Illumina for rare and undiagnosed diseases research. Starting from library prep to sequencing and informatics, Illumina empowers researchers to find the answers they seek in rare and undiagnosed disease research.
GenomeStudio - Creating Custom Cluster Files
Webinar
Mar 19
GenomeStudio - Creating Custom Cluster Files
Mar 19, 2025
Using GenomeStudio software to generate custom cluster files is necessary to analyse custom microarray content. In this webinar, we discuss the basics of cluster files including when to use a custom cluster file, why custom cluster files are needed, as well as the detailed steps required to create your own custom cluster file. Learn how to cluster the SNPs on your custom array by properly filtering and manually editing the file.