Efficient querying of genomic reference databases with gget.
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- Record sourced from PubMed, PMID 36610989.
- Also identified by DOI 10.1093/bioinformatics/btac836 and PMC identifier 9835474.
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Abstract
A recurring challenge in interpreting genomic data is the assessment of results in the context of existing reference databases. With the increasing number of command line and Python users, there is a need for tools implementing automated, easy programmatic access to curated reference information stored in a diverse collection of large, public genomic databases. gget is a free and open-source command line tool and Python package that enables efficient querying of genomic reference databases, such as Ensembl. gget consists of a collection of separate but interoperable modules, each designed to facilitate one type of database querying required for genomic data analysis in a single line of code. The manual and source code are available at https://github.com/pachterlab/gget. Supplementary data are available at Bioinformatics online.
Medical subject headings
- Genomics
- Software