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.
[in development] Proof-of-Concept variation translation, validation, and registration service
biocommons website
non-redundant, compressed, journalled, file-based storage for biological sequences
OpenAPI-based REST interface to biological sequences and sequence metadata
provides common tools and lookup tables used primarily by the hgvs and uta packages
Python library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`
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