Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gaps
- First Published November 1, 2024
A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities
- First Published October 29, 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