4 open source projects by biocommons

Python library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`

Universal Transcript Archive: comprehensive genome-transcript alignments; multiple transcript sources, versions, and alignment methods; available as a docker image

simplified searching, fetching, and parsing records from NCBI using their E-utilities interface

non-redundant, compressed, journalled, file-based storage for biological sequences