Python library to parse, format, validate, normalize, and map sequence variants according to HGVS Nomenclature (https://hgvs-nomenclature.org/).
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Updated
Nov 5, 2025 - Python
Python library to parse, format, validate, normalize, and map sequence variants according to HGVS Nomenclature (https://hgvs-nomenclature.org/).
non-redundant, compressed, journalled, file-based storage for biological sequences
Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets
provides common tools and lookup tables used primarily by the hgvs and uta packages
[in development] Proof-of-Concept variation translation, validation, and registration service
OpenAPI-based REST interface to biological sequences and sequence metadata
The code provides a collection of functions for various statistical calculations, including sorting, frequency analysis, mean calculations, and dispersion measures.
Script for generating randomized exams with questions and answers randomization using LaTeX and Python.
biocommons website
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