1195 views | 1 decade ago
In this supplemental video we go behind the science of Adventures in Genomics: Archeology of the invisible: https://youtu.be/JTh5baW01Nc TABLE OF CONTENTS: Introduction: 00:38 Calcification: 01:30 DNA...
1185 views | 9 years ago
Hear how Jonathan Mill, PhD, group leader of the complex disease epigenetics group at the University of Exeter Medical School, is using genetic information to study the causes of molecular variation...
1175 views | 5 years ago
Moderator: Alex Aravanis, Illumina Panelists: Christina Curtis, Stanford University; Joel Dudley, Tempus; Elli Papaemmanuil, Memorial Sloan Kettering Cancer Center Description: As methods to analyze...
1174 views | 7 years ago
In chapter 4, industry thought leaders explore how polygenic risk scores will one day impact clinical care—as early predictors of disease, when there is an unclear diagnosis, and early detection of...
1170 views | 10 years ago
Illumina dedicates the Jay T. Flatley Innovation Center to honor longtime CEO, Jay Flatley. New Innovation Gallery offers a look back at Illumina's history and Flatley's legacy. See his surprise reaction...
1169 views | 10 years ago
Learn how DNA sequencing is leading to progress in the rapid identification of variants that might be involved in genetic diseases. Thanks to this work, Dr Kingsmore and his team now hold a Guinness...
1169 views | 1 decade ago
Christopher Mason, Assistant Professor in the Department of Physiology and Biomedicine at the Weill Cornell Medical College, describes how tumor evolution can be tracked by sequencing the transcriptome,...
1161 views | 4 years ago
This video shows best practices on how to network Illumina® benchtop instruments with Windows 10 OS. Specifically instruments with NextSeq™ Control Software v4.0.1 or later, MiniSeq™ Control Software...