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Michael Rossi: Advancing Clinical Cancer Research With NGS

438 views | 8 years ago

Michael Rossi, Phd discusses the important role of next-generation sequencing (NGS) in clinical cancer research. www.illumina.com/cancer Dr. Rossi explains how NGS enables researchers to cost-effectively...

Agrigenomic Tools: Powered by Illumina — From Discovery to Decision

438 views | 9 years ago

Illumina genomic solutions improve plant and animal selection, nutrition, health surveillance, traceability, and veterinary diagnostics systems. The award-winning, industry-standard array portfolio...

Discovering a Causal Somatic Mutation in Patients with Sturge-Weber

436 views | 1 decade ago

Discovering a Causal Somatic Mutation in Patients with Sturge-Weber Syndrome with Dr. Jonathan Pevsner

Genes in the Bottle

433 views | 8 years ago

If your wish is a great bottle of wine, forget about the genie. It’s the genes in the bottle that matter. In this week’s SciMon video, learn how microbes, genes, and the environment all collaborate...

Talia & Dan H. | A Noninvasive Prenatal Screening Patient Success Story

430 views | 9 years ago

After two miscarriages, couple Talia and Dan worried whether they could conceive a healthy child. The third time they became pregnant, they tried noninvasive prenatal testing (NIPT)—a screening test...

How to Open the Tumor/Normal Sequencing Data in BaseSpace

425 views | 1 decade ago

This video describes how to log into BaseSpace to access the Tumor/Normal Sequencing data. It also provides a brief description of BaseSpace Project page including Quick Launch buttons and hyperlinks,...

Illumina Video: Accelerating Agrigenomic Breakthroughs with Genomics

420 views | 8 years ago

Celebrating 10 years of progress powered by the award-winning Infinium® Array, Illumina genomic solutions are shaping the future of agricultural genomics. Improve plant and animal selection, nutrition,...

Every Diagnosis Matters

416 views | 5 years ago

We are on the brink of a breakthrough and there is new hope for families facing rare and undiagnosed genetic diseases. The value of a definitive diagnosis stops the guessing, grows our understanding...