SeqVarTools
SeqVarTools provides efficient access, management, and analysis of Variant Call Format (VCF) data for large-scale genomic studies.
Key Features:
- Fast-Access Storage: Utilizes SeqArray's optimized storage format to enable rapid retrieval and manipulation of Variant Call Format (VCF) files.
- Common Operations: Implements filtering, subsetting, and annotation operations for VCF data.
- Interoperability with Bioconductor: Integrates with the Bioconductor ecosystem of over 934 interoperable packages within the R programming environment for statistical and bioinformatic analyses.
Scientific Applications:
- Variant Analysis: Facilitates detailed examination of genetic variants for population genetics, disease association, and evolutionary biology studies.
- Data Integration: Enables integration with Bioconductor packages for expression data correlation and pathway analysis.
Methodology:
Operates within the R programming environment, uses SeqArray for fast-access storage of VCF data, and follows Bioconductor's formal initial review and continuous automated testing processes.
Topics
Collections
Details
- License:
- GPL-3.0
- Tool Type:
- command-line tool, library
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- R
- Added:
- 1/17/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Huber W, Carey VJ, Gentleman R, Anders S, Carlson M, Carvalho BS, Bravo HC, Davis S, Gatto L, Girke T, Gottardo R, Hahne F, Hansen KD, Irizarry RA, Lawrence M, Love MI, MacDonald J, Obenchain V, Oleś AK, Pagès H, Reyes A, Shannon P, Smyth GK, Tenenbaum D, Waldron L, Morgan M. Orchestrating high-throughput genomic analysis with Bioconductor. Nature Methods. 2015;12(2):115-121. doi:10.1038/nmeth.3252. PMID:25633503. PMCID:PMC4509590.