Metadata-Version: 2.1
Name: mavehgvs
Version: 0.2.1
Summary: Regular expression-based validation of HGVS-style variant strings for Multiplexed Assays of Variant Effect.
Home-page: https://github.com/VariantEffect/mavehgvs
Author: Daniel Esposito and Alan F Rubin
Author-email: alan.rubin@wehi.edu.au
License: UNKNOWN
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        # mavehgvs
        mavehgvs is the Python reference implementation of the MAVE-HGVS variant representation standard,
        a strict subset of [HGVS](http://varnomen.hgvs.org/), used primarily for clinical genomics.
        
        ## The MAVE-HGVS Standard
        MAVE-HGVS is a strict subset of the [HGVS Sequence Variant Nomenclature](https://varnomen.hgvs.org/), version 20.05.
        HGVS nomenclature is comprehensive and very expressive and consequently includes a lot of syntax that is not needed to
        represent variants from Multiplexed Assay of Variant Effect (MAVE) data and makes the variant strings more challenging 
        to parse.
        
        While packages exist for parsing HGVS (most notably the
        [biocommons hgvs package](https://github.com/biocommons/hgvs/), they are intended for use in human genetics and
        rely on sequence databases and reference sequence (called "target sequence" for MAVE-HGVS), which are not always
        available for or relevant for multiplexed assays.
        
        MAVE-HGVS is an attempt to define an easy-to-parse subset of the HGVS nomenclature that captures those variants that
        occur in MAVE datasets, while excluding many variant types that are unlikely to be found. Importantly, the
        mavehgvs implementation does not rely on external sequence databases or identifiers.
        
        ## Supported Variants
        MAVE-HGVS supports DNA, RNA, and protein variants.
        MAVE-HGVS supports a subset of HGVS variants including:
        
        * substitutions
        * deletions
        * duplications
        * insertions
        * frame shifts
        
        Many HGVS variants are unsupported including:
        
        * inversions
        * conversions
        * extensions
        * changes in methylation state
        * RNA fusion transcripts
        * mosaicism
        * chimerism
        * variants with uncertain consequence
        * variants in trans or unknown phase
        * complex variants (e.g. translocations)
        
        For further details, including example variants, see the specification in the package documentation.
        
        # Installation
        Install mavehgvs from pip using:
        
        ```bash
        pip3 install mavehgvs
        ```
        
        # Feedback
        To report a problem or request a new feature with either the mavehgvs package or the MAVE-HGVS standard,
        please use the GitHub issue tracker.
        
Platform: UNKNOWN
Classifier: Development Status :: 3 - Alpha
Classifier: Intended Audience :: Science/Research
Classifier: Topic :: Scientific/Engineering :: Bio-Informatics
Classifier: License :: OSI Approved :: BSD License
Classifier: Programming Language :: Python :: 3
Classifier: Operating System :: OS Independent
Requires-Python: >=3.6
Description-Content-Type: text/markdown
