PyPI
broadinstitute/viral-ngs
viral-ngs: command line tools and wrappers for processing raw viral genomic data
MITOct 19, 2026 · metrics 2.10.0
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#variant-calling
Every repository in the public record carrying this tag — from its GitHub topics or the keywords its package registries publish. Health is measured under the same versioned methodology as the rest of the record.
6 records
PyPI · npm
haqaliz/contig
An agentic bioinformatics analyst: it runs the analysis on your own compute, self-heals failures, verifies the output, and returns a reproducible result.
Apache-2.0Oct 21, 2026 · metrics 2.10.0
PyPI
kcleal/dysgu
Toolkit for calling structural variants using short or long reads
MITSep 13, 2026 · metrics 2.10.0
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MPUSP/snakemake-simple-mapping
A Snakemake workflow for the mapping of reads to reference genomes, minimalistic and simple.
MITSep 14, 2026 · metrics 2.10.0
PyPI · npm
smartsbio/smarts-bio-jupyterlab
No repository description published.
MITSep 9, 2026 · metrics 2.10.0
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PacificBiosciences/ccs
CCS: Generate Highly Accurate Single-Molecule Consensus Reads (HiFi Reads)
BSD-3-Clause-ClearSep 13, 2026 · metrics 2.10.0