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

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 anomaly detector

Extensible specification for representing and uniquely identifying biological sequence variation

Integrative analysis of structural variations.

Datastructures and algorithms for working with genetic variation

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

dbVar

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

A memory efficient tool to map and visualize evolutionary regions

OpenAPI-based REST interface to biological sequences and sequence metadata

Python package for slightly or massively variating numbers within a certain range and based on one central point.

Web site for the paper "Conducting and Analyzing Human Studies: The Role of Variation and Aggregation"

Site internet pour visualiser les variations et les signes d'une fonction en dressant son tableau de variations ou de signes.

Organization-wide GitHub configuration

The code provides a collection of functions for various statistical calculations, including sorting, frequency analysis, mean calculations, and dispersion measures.

biocommons website

This QGIS plugin creates vector layers that work with magnetic variation.