Python library to parse, format, validate, normalize, and map sequence variants according to HGVS Nomenclature (https://hgvs-nomenclature.org/).

Extensible specification for representing and uniquely identifying biological sequence variation

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

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

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

Datastructures and algorithms for working with genetic variation

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

dbVar

OpenAPI-based REST interface to biological sequences and sequence metadata

Integrative analysis of structural variations.

[in development] Proof-of-Concept variation translation, validation, and registration service

biocommons website

Semester project for the subject of Probability and Statistics, a subject attended at Centro Universitário FEI. It consists of analyzing a database

A memory efficient tool to map and visualize evolutionary regions

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

REST service over https://github.com/biocommons/uta/

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

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

Geographic Variation in the Prevalence of Behavioral Disorders among Children and Adolescents in Arkansas