Understanding the genomic complexity of human genetic disorders

Author:

QIAGEN Digital Insights

Understanding the genomic complexity of human genetic disorders

Webinar: Unraveling the genomic complexity of common and rare genetic disorders

NGS bioinformatics for the discovery of causal variants

 

Rajini R. Haraksingh, PhD, Postdoctoral Fellow, Stanford University and Vice Precident, Rare Genomics Institute presents some approaches to how to discover causal variants in different types of diseases.

 

Share on:


Tags