Varuna Chander

This study uses a deep learning framework to analyze whole-genome data from ME/CFS patients, identifying risk genes and linking them to disease symptoms and other complex traits.

The paper describes the role of the Centers for Mendelian Genomics in advancing gene discovery through data sharing, collaboration, and resource development over the past decade.

This study evaluates five SV genotyping software methods using simulated and real data to assess their sensitivity, reliability, and compatibility with VCF formats.