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hgvs
PublicPython library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`biocommons.seqrepo
Publicnon-redundant, compressed, journalled, file-based storage for biological sequencesanyvar
Public[in development] Proof-of-Concept variation translation, validation, and registration serviceuta
PublicUniversal Transcript Archive: comprehensive genome-transcript alignments; multiple transcript sources, versions, and alignment methods; available as a docker imagebioutils
Publicprovides common tools and lookup tables used primarily by the hgvs and uta packagesbiocommons.example
Public templateseqrepo-rest-service
PublicOpenAPI-based REST interface to biological sequences and sequence metadatabiocommons.github.io
Publicbiocommons websiteeutils
Public.github
PublicOrganization-wide GitHub configurationuta-align
PublicC-based Needleman-Wunsch and Smith-Waterman alignment algorithms with a Python interface.hgvs-eval
Publiclogos
Publichgvs-dataproviders-rest
Publicmirrors-ncbi
PublicMakefile (of all things) to space-efficiently mirror selected NCBI resourceshackathon-2023
Public archiveuta-clients
Publicdockerbase
Publichgvs-installation-test
Publicbiocommons-python
Public