variation topic

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

biocommons

Library for multi-dimensional, multi-sensor, uni/multivariate time series data analysis, unsupervised feature selection, unsupervised deep anomaly detection, and prototype of explainable AI for anomal...

ajayarunachalam

Extensible specification for representing and uniquely identifying biological sequence variation

ga4gh

dbVar

ncbi

Integrative analysis of structural variations.

YaoLab-Bioinfo

Datastructures and algorithms for working with genetic variation

BioJulia

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

biocommons

Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets

pughlab

provides common tools and lookup tables used primarily by the hgvs and uta packages

biocommons