Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets
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Updated
Jul 30, 2020 - Python
Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets
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.
OpenAPI-based REST interface to biological sequences and sequence metadata
non-redundant, compressed, journalled, file-based storage for biological sequences
Variation Nodes for ComfyUI automation workflows | https://www.scuffedepoch.com | https://www.oragenai.com |ORAGEN TEAM
Python library to parse, format, validate, normalize, and map sequence variants according to HGVS Nomenclature (https://hgvs-nomenclature.org/).
provides common tools and lookup tables used primarily by the hgvs and uta packages
biocommons website
Lightweight, portable variation registration and retrieval
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