An introduction to NGS technology and applications for labs.
Trilochan Sahoo, MD discusses the benefits of the CytoSNP-850K BeadChip array.
Drs. Koehler and Benet-Pages are using the Infinium CytoSNP-850K BeadChip and the TruSight Cancer Panel to analyze chromosomal abnormalities.
Download the handout on the Importance of Carrier Screening
Learn how the NextSeq 550 is enhancing research in reproductive and genetic health and why it’s being rapidly adopted in genetic testing labs. Get a glimpse into the advantages of this integrated, cost-effective solution for diverse applications.
The couple reflects on the value of NIPT and its ability to provide couples like them with more accurate answers.
For tips about how to choose the best sequencer and transform your lab, download the Buyer's Guide to Next-Generation Sequencing Systems.
Preimplantation genetic diagnosis can be used where there is a risk of severe genetic disorders being inherited from parents. Join Professor Alan Handyside and Alan Thornhill as they introduce the Illumina karyomapping solution.
Learn how karyomapping offers a rapid PGD solution for single-gene disorders.
Alan Handyside reviews the significant breakthroughs in preimplantation genetics since the first live birth following IVF with PGD.
Watch Dagan Wells discuss how PGS through NGS improves IVF success.
Hear Simon Fishel talk about screening all 24 chromosomes with PGS.
Simon Fishel shares how VeriSeq is built to handle high throughput demand with speed and accuracy.
Listen as Francesco Fiorentino discusses the high-throughput, high-resolution advantages of NGS.
Listen as Tony Gordon shares his vision for better IVF clinical outcomes using NGS.
Hear Tony Gordon discuss how the Illumina portfolio empowers reproductive health labs.
Dr. Robert Anderson discusses pregnancy rates achieved with PGS.
Listen to Dr. Robert Anderson share the benefits of single embryo transfer enabled by PGS.
Dr. Robert Anderson shares how a lab achieves a high IVF success rate with PGS.
Learn how PGS and PGD solutions can produce accurate genomic information for optimized embryo selection and more informed decisions about reproductive options.
A brief, educational primer about next-generation sequencing for in vitro fertilization.
Share this brochure with your patients to educate them about PGS and how it can improve IVF success rates.
Join Angie Beltsos, MD, as she explores the latest advancements in fertility. Topics include minimizing risk of hyperstimulation, optimizing health of the transferred embryo, and improving the odds…
Dr. Robert Anderson, Director of the Southern California Center for Reproductive Medicine and Medical Director for the Southern California Institute for Reproductive Sciences, discusses how preimplantation…
Childhood sweethearts, now husband and wife, Vy and Kyle share their personal in vitro fertilization success story. You ll hear how Illumina preimplantation genetic screening (PGS) helped them fulfill…
Innovative BlueFuse Multi Software
A video for parents to be to learn more about noninvasive prenatal testing.
To learn more about the benefits of an expanded CF screen, read “Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene.” by PR Sosnay, et al.
Learn how the application of NGS in clinical PGS cycles allows for identification and transfer of euploid embryos resulting in ongoing pregnancies.
Prenatal testing with the use of cfDNA has significantly lower false positive rates and higher positive predictive values for detection of trisomies 21 and 18 than standard screening.
A poster presentation from the 2015 Annual Meeting of the Society for Maternal- Fetal Medicine.
Noninvasive prenatal testing in the general obstetric population.
Simon Fishel describes how preimplantation genetic screening (PGS) and preimplantation genetic diagnosis (PGD) enable selection of embryos free of chromosomal problems for transfer.
Learn about the MiSeqDX Cystic Fibrosis System in this quick tutorial
Discover the use of arrays to investigate individuals with intellectual disability, developmental delay, autism, and congenital abnormalities.
See vital statistics around sudden cardiac arrest, one of the leading causes of non-traumatic fatality in the US.
Know your options in prenatal testing with an educational video on NIPT.
Professor Yuval Yaron discusses the implications of test failures.
Dr. Alan Handyside discusses how selective implantation of euploid embryos can lead to increased pregnancy rates.
Share this brochure with your patients to educate them about PGD.
View all 174 genes, related to 17 ICCs, detected by the TruSight Cardio Sequencing Kit.
Data shows Illumina next-generation sequencing is the NIPT technology of choice.
Embryologists from all over the world gathered for the Global Embryology Summit, an exclusive event featuring hands-on instructor-led workshops designed by fellow embryologists to improve best practices…
Maternal fetal medicine specialist Dr. Tracy Prosen highlights the differences between screening and diagnostic prenatal tests.
Key opinion leaders in the fields of preimplantation genetic screening (PGS) and preimplantation genetic diagnosis (PGD) discuss how partnering with Illumina has positively impacted families around the world.
Dr. Stuart Cook explains how targeted analysis with the TruSight Cardio Sequencing Kit can uncover inherited cardiac conditions.
Dr. Ali Hellani discusses his passion to help couples undergoing IVF by providing them with reliable genetic screening technologies.
Noninvasive prenatal screening (NIPT) was found cost-effective as first line screening for all pregnant women.
Noninvasive prenatal testing (NIPT) helps reduce the need for invasive procedures
Pam and Eric share how transferring a single embryo with PGS helped them start a family while they balanced their busy lifestyles.
Visual aids for patient discussions about reproductive genetic concepts such as PGS and NIPT.
Viafet enables IVF clinics throughout the Middle East and Australia to provide fast, accurate, and efficient PGS services.
Whole-genome sequencing can potentially broaden and foreshorten differential diagnosis, resulting in fewer empirical treatments and faster progression to genetic and prognostic counseling.
Learn how Dr Kenjiro Kosaki furthers his clinical research and expands the genetic analysis services he provides with TruSight One Sequencing Panel.
Hear from Dr Heidi Rehm and learn how she is identifying the causal variants of cardiomyopathy.
Learn how Dr Stephen Kingsmore aided in decoding the genomes of children being seen at Children’s Mercy Hospital.
Whole-genome noninvasive prenatal testing provides results when another test was inconclusive.
Learn more about the Verifi Prenatal Test—a reliable, easy, fast, noninvasive prenatal test.
Study published in NEJM finds Verifi Prenatal Test achieves 10×higher positive predictive value vs. current standard of care.
Learn about a randomized controlled trial comparing pregnancy rates following VeriSeq PGS versus standard morphology for elective single embryo transfer.
Dr. Glenn Palomaki shares his data and expert opinion on the clinical utility of NIPT in the general pregnancy population.
Learn about our partnerships with professional societies and organizations—striving together to advance awareness of genetics and health.
Discovering rare chromosomal abnormalities using WGS-based NIPT.
Learn how the Verifi Prenatal Test uses proven NGS technology to provide accurate NIPT results.
Martin Chavez, MD, a maternal-fetal medicine specialist, discusses noninvasive prenatal testing.
Dr. Chavez discusses the benefits of NIPT for prenatal screening of fetal chromosomal aneuploidies.
Noninvasive prenatal screening (NIPT) was found cost-effective as first line screening for all pregnant women.
An overview of recent publications featuring Illumina solutions for preimplantation genetics technology.