A map of enhancer regions in primary human neural progenitor cells using capture STARR-seq
- First Published July 11, 2025
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
Read clouds uncover variation in complex regions of the human genome
- First Published August 18, 2015