T2T-CHM13 improves read mapping and detection of clinically relevant genetic variation in the Swedish population
- First Published September 16, 2025
Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T
- First Published March 17, 2025
Gapless assembly of complete human and plant chromosomes using only nanopore sequencing
- First Published November 6, 2024
Phased nanopore assembly with Shasta and modular graph phasing with GFAse
- First Published April 16, 2024
HiCanu: accurate assembly of segmental duplications, satellites, and allelic variants from high-fidelity long reads
- First Published August 14, 2020