grabseqs: simple downloading of reads and metadata from multiple next-generation sequencing data repositories.
basic_science · Level V
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- Record sourced from PubMed, PMID 32154830.
- Also identified by DOI 10.1093/bioinformatics/btaa167 and PMC identifier 7267817.
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Abstract
High-throughput sequencing is a powerful technique for addressing biological questions. Grabseqs streamlines access to publicly available metagenomic data by providing a single, easy-to-use interface to download data and metadata from multiple repositories, including the Sequence Read Archive, the Metagenomics Rapid Annotation through Subsystems Technology server and iMicrobe. Users can download data and metadata in a standardized format from any number of samples or projects from a given repository with a single grabseqs command. Grabseqs is an open-source tool implemented in Python and licensed under the MIT license. The source code is freely available at https://github.com/louiejtaylor/grabseqs, the Python Package Index and Anaconda Cloud repository. bushman@pennmedicine.upenn.edu. Supplementary data are available at Bioinformatics online.
Medical subject headings
- High-Throughput Nucleotide Sequencing
- Metadata