Research
Characterizing cytosine methylation of polymorphic transposable element insertions using the human pangenome resources
- First Published May 14, 2026
Research
Centromeric instability and chromoanasynthesis observed in nine supernumerary marker chromosomes resolved with long-read genome sequencing
- First Published March 25, 2026
Research
Assessing DNA methylation detection for primary human tissue using Nanopore sequencing
- First Published March 7, 2025
Research
Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gaps
- First Published November 1, 2024
Research
Resolving complex duplication variants in autism spectrum disorder using long-read genome sequencing
- First Published October 29, 2024
Research
A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities
- First Published October 29, 2024
Method
Phased nanopore assembly with Shasta and modular graph phasing with GFAse
- First Published April 16, 2024
Research
Gaps and complex structurally variant loci in phased genome assemblies
- First Published May 10, 2023
Method
A complete pedigree-based graph workflow for rare candidate variant analysis
- First Published April 28, 2022