Know your options in prenatal testing with an educational video on NIPT.
Dagan Wells describes how high-throughput, next-generation sequencing for PGS to detect aneuploid embryos is a game changer for IVF clinics and labs.
Listen as Francesco Fiorentino discusses the high-throughput, high-resolution advantages of NGS.
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.
Dr. Stuart Cook explains how targeted analysis with the TruSight Cardio Sequencing Kit can uncover inherited cardiac conditions.
Learn about the MiSeqDX Cystic Fibrosis System in this quick tutorial
Dr. Ali Hellani discusses his passion to help couples undergoing IVF by providing them with reliable genetic screening technologies.
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.
Maternal fetal medicine specialist Dr. Tracy Prosen highlights the differences between screening and diagnostic prenatal tests.
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.
Professor Yuval Yaron discusses the implications of test failures.
Innovative BlueFuse Multi Software
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…
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…
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…
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…
A video for parents to be to learn more about noninvasive prenatal testing.
The couple reflects on the value of NIPT and its ability to provide couples like them with more accurate answers.
Dr. Robert Anderson shares how a lab achieves a high IVF success rate with PGS.
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.
Alan Handyside reviews the significant breakthroughs in preimplantation genetics since the first live birth following IVF with PGD.
Dr. Alan Handyside discusses how selective implantation of euploid embryos can lead to increased pregnancy rates.
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.
Simon Fishel describes how preimplantation genetic screening (PGS) and preimplantation genetic diagnosis (PGD) enable selection of embryos free of chromosomal problems for transfer.
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.
Listen to Dr. Robert Anderson share the benefits of single embryo transfer enabled by PGS.
Dr. Robert Anderson discusses pregnancy rates achieved with PGS.
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.
Discover the use of arrays to investigate individuals with intellectual disability, developmental delay, autism, and congenital abnormalities.
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.
Noninvasive prenatal testing in the general obstetric population.
Noninvasive prenatal screening (NIPT) was found cost-effective as first line screening for all pregnant women.
An introduction to NGS technology and applications for labs.
See vital statistics around sudden cardiac arrest, one of the leading causes of non-traumatic fatality in the US.
Learn more about the MiSeqDx Cystic Fibrosis System.
Drs. Koehler and Benet-Pages are using the Infinium CytoSNP-850K BeadChip and the TruSight Cancer Panel to analyze chromosomal abnormalities.
Trilochan Sahoo, MD discusses the benefits of the CytoSNP-850K BeadChip array.
View all 174 genes, related to 17 ICCs, detected by the TruSight Cardio Sequencing Kit.
Read valuable information on sudden cardiac arrest and the relation to inherited cardiac conditions.
Download the handout on the Importance of Carrier Screening
Data shows Illumina next-generation sequencing is the NIPT technology of choice.
A poster presentation from the 2015 Annual Meeting of the Society for Maternal- Fetal Medicine.
Share this brochure with your patients to educate them about PGS and how it can improve IVF success rates.
A brief, educational primer about next-generation sequencing for in vitro fertilization.
Learn how PGS and PGD solutions can produce accurate genomic information for optimized embryo selection and more informed decisions about reproductive options.
Learn how the application of NGS in clinical PGS cycles allows for identification and transfer of euploid embryos resulting in ongoing pregnancies.
Share this brochure with your patients to educate them about PGD.
For tips about how to choose the best sequencer and transform your lab, download the Buyer's Guide to Next-Generation Sequencing Systems.
Learn how karyomapping offers a rapid PGD solution for single-gene disorders.
Discover the synergy of next-generation sequencing and arrays.
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.
Study published in NEJM finds Verifi Prenatal Test achieves 10×higher positive predictive value vs. current standard of care.
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.
Learn how Dr Kenjiro Kosaki furthers his clinical research and expands the genetic analysis services he provides with TruSight One Sequencing Panel.
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 Stephen Kingsmore aided in decoding the genomes of children being seen at Children’s Mercy Hospital.
Hear from Dr Heidi Rehm and learn how she is identifying the causal variants of cardiomyopathy.
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 how the Verifi Prenatal Test uses proven NGS technology to provide accurate NIPT results.
Discovering rare chromosomal abnormalities using WGS-based NIPT.
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.
Learn about our partnerships with professional societies and organizations—striving together to advance awareness of genetics and health.