Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gaps
- First Published November 1, 2024
Resolving complex duplication variants in autism spectrum disorder using long-read genome sequencing
- First Published October 29, 2024
A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities
- First Published October 29, 2024
The ethics of conducting molecular autopsies in cases of sudden death in the young
- First Published July 13, 2016