Complete genetic and epigenetic architecture of D4Z4 macrosatellites in FSHD, BAMS, and reference cohorts with D4Z4End2End
- First Published March 23, 2026
Measuring X-Chromosome inactivation skew for X-linked diseases with adaptive nanopore sequencing
- First Published September 16, 2024
A complete pedigree-based graph workflow for rare candidate variant analysis
- First Published April 28, 2022
Comparative Annotation Toolkit (CAT)—simultaneous clade and personal genome annotation
- First Published June 8, 2018
An extended set of yeast-based functional assays accurately identifies human disease mutations
- First Published March 14, 2016