Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T
- First Published March 17, 2025
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
Systematic characterization of A-to-I RNA editing hotspots in microRNAs across human cancers
- First Published April 14, 2017