T2T-CHM13 improves read mapping and detection of clinically relevant genetic variation in the Swedish population
- First Published September 16, 2025
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
Visualization and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR
- First Published August 15, 2024