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The most affordable Illumina system, designed for everyday sequencing
Kits & Reagents
Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information
Find specifications and project recommendations for kits such as Nextera XT DNA using the Kit Selector tool
Software & Informatics Products
Mine over 20,000 genomic studies to get data-driven answers for genes, experiments, drugs and phenotypes for your research
Verify instrument installation and operation, and obtain an audit-ready report
Reagent kits for the NovaSeq 6000 System provide ready-to-use cartridge-based reagents for cluster generation and SBS
Low NovaSeq 6000 System sequencing costs spark new projects and customer growth
Survey finds Americans unaware of DNA's power to improve lives
All Legal Information
Complimentary and secure instrument monitoring can help you avoid unplanned downtime
All Support Tools
Product Support Services
Deep, comprehensive, and accessible sequencing power for detecting solid tumor biomarkers
Cancer Genomics Products
Microbial Genomics Research
Local scientists analyze transmission patterns and trace origin of Ebola outbreak in the Democratic Republic of Congo
Microbial Genomics Products
A rapidly emerging method for studying biodiversity and monitoring ecosystem changes
Complex Disease Research Products
Families facing rare diseases often spend years pinpointing the problem in solitude – until now
In podcast episode 41, Dr. Åke Borg discusses developing better biomarkers for risk stratification of individuals with breast cancer
Rethink prenatal screenining. Think VeriSeq NIPT.
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Perform transcriptome profiling for hundreds to tens of thousands of single cells in one experiment.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.
Learn how Illumina next-generation sequencing (NGS) works, and how it's furthering forensic science.
Find out how deep mitochondrial DNA (mtDNA) sequencing is being used to identify skeletal remains.
Fast library prep delivers quality de novo assembly of small genomes.
Instructions for human mtDNA D-loop hypervariable region sample preparation.
Instructions for human mtDNA genome sample preparation.
Improved human mtDNA analysis using NGS and cloud-based computing and storage.
Researchers use NGS to obtain more information-rich data and answer more complex forensic questions.
Criminalists use MiSeq FGx for high-resolution DNA profiling to build better forensic DNA databases.
Researchers identify genetic variants that influence facial features to enable facial imaging from DNA.
Learn about the advantages of targeted NGS and view the data validating the MiSeq FGx System in this Forensic Magazine article.
Learn about the potential of NGS to solve cold missing persons cases and identify unknown human remains.
In forensic work, the smallest detail can make the difference in solving a crime.
Hear from experts in the field how massively parallel sequencing (MPS) is paving the way ahead, and why now is the time to adopt it.
Learn how the Illumina forensic genomics workflow can transform forensic applications.
Dr. Mitch Holland of Penn State explains how NGS is helping us realize the power of mtDNA heteroplasmy.
The MiSeq FGx System is the first fully validated NGS solution designed exclusively for forensic science.
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