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- hgvs Public Forked from biocommons/hgvs
Python library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`
genomoncology/hgvs’s past year of commit activity - biocommons.seqrepo Public Forked from biocommons/biocommons.seqrepo
non-redundant, compressed, journalled, file-based storage for biological sequences
genomoncology/biocommons.seqrepo’s past year of commit activity - pysam Public Forked from pysam-developers/pysam
Pysam is a Python package for reading, manipulating, and writing genomics data such as SAM/BAM/CRAM and VCF/BCF files. It's a lightweight wrapper of the HTSlib API, the same one that powers samtools, bcftools, and tabix.
genomoncology/pysam’s past year of commit activity - swagger-codegen Public Forked from swagger-api/swagger-codegen
swagger-codegen contains a template-driven engine to generate documentation, API clients and server stubs in different languages by parsing your OpenAPI / Swagger definition.
genomoncology/swagger-codegen’s past year of commit activity - hgvs-rs Public Forked from varfish-org/hgvs-rs
A port of biocommons/hgvs to the Rust programming language
genomoncology/hgvs-rs’s past year of commit activity
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