Scalable gVCF merging and joint variant calling for population sequencing projects
updated at April 27, 2024, 2:06 p.m.
DELLY2: Structural variant discovery by integrated paired-end and split-read analysis
updated at April 26, 2024, 12:25 p.m.
A fast and sensitive gapped read aligner
updated at April 26, 2024, 6:07 a.m.
Bayesian haplotype-based mutation calling
updated at April 13, 2024, 5:26 a.m.
C++ API & command-line toolkit for working with BAM data
updated at March 22, 2024, 8 a.m.