Python library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`
-
Updated
Jul 29, 2024 - Python
Python library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`
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.
biocommons website
Script for generating randomized exams with questions and answers randomization using LaTeX and Python.
Add a description, image, and links to the variation topic page so that developers can more easily learn about it.
To associate your repository with the variation topic, visit your repo's landing page and select "manage topics."