Year: 2015
Type: article
Abstract: Genomic technologies present powerful tools with the potential to diagnose, treat, and elucidate the underpinnings of human disease. Technological advances have allowed researchers and clinicians to apply novel approaches and gain statistical power to delve more deeply and broadly into our genomes than ever before, enabling them to discover associations between genomic variants and disease phenotypes that were previously beyond our reach. In this webinar, we will explore how genomics is currently being applied to characterize rare disease and cancer, highlight recent advances in these respective areas, and look toward the future to predict what is needed to positively impact human health. View the Webinar
Source: Science
Authors: Daniel MacArthur, Eliezer Van Allen
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: bronze
OpenAlex ID: W260650226