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    • Scripts and containers to run germline variant callers
      Shell
      0000Updated Jan 29, 2026Jan 29, 2026
    • Scripts and containers to run somatic variant callers
      Shell
      0000Updated Jan 29, 2026Jan 29, 2026
    • Tool for adding genomic variants to an existing genome (in SAM/BAM/CRAM format). Currently supported variants are SNVs, indels and SVs (insertions, deletions, t…
      Python
      1100Updated Nov 4, 2025Nov 4, 2025
    • Lightweight and memory efficient reader for PLINK BED files. It supports both SNP-major and individual-major formats. Written in Python.
      Python
      0300Updated Feb 21, 2025Feb 21, 2025
    • Tool for copying read-alignments regions centered around variants (in VCF/VCF.GZ/BCF format) from existing genomes (in SAM/BAM/CRAM format) to concat them into …
      Python
      1100Updated Sep 12, 2024Sep 12, 2024