gdtools_gd2vcf
gdtools_gd2vcf converts Genome Diff (GD) files into Variant Call Format (VCF) files to represent and document sequence variants for downstream genetic analyses.
Key Features:
- Conversion Capability: Transforms Genome Diff (GD) files into VCF files to represent and document mutations present in input data.
- Galaxy Integration: Operates within the Galaxy platform and can run on the Institut Pasteur Galaxy instance with its suite of over 280 tools.
- API / Library Interface: Communicates with Galaxy using the Galaxy API or the Bioblend library to execute workflows and manage jobs.
- Standardized Output: Produces standardized VCF outputs suitable for downstream variant analysis and data interoperability.
- Resource Utilization: Leverages Galaxy as the execution engine to utilize centralized computational resources on the Institut Pasteur cluster.
Scientific Applications:
- Mutation Analysis: Enables identification and documentation of mutations by converting GD-derived differences into VCF variant calls.
- Comparative Genomics: Facilitates comparative genomics by translating Genome Diff comparisons into a common VCF format.
- Evolutionary Biology: Supports evolutionary analyses by providing variant call representations derived from Genome Diff data.
- Data Sharing and Interoperability: Produces VCF outputs that enable sharing and comparison of variant data across projects and tools.
Methodology:
Converts Genome Diff (GD) records to Variant Call Format (VCF) and interfaces with a Galaxy instance via the Galaxy API or the Bioblend library for job execution on the Institut Pasteur cluster.
Topics
Collections
Details
- Maturity:
- Mature
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 12/19/2016
- Last Updated:
- 6/16/2020
Operations
Data Inputs & Outputs
Formatting
Outputs
Publications
Barrick JE, Colburn G, Deatherage DE, Traverse CC, Strand MD, Borges JJ, Knoester DB, Reba A, Meyer AG. Identifying structural variation in haploid microbial genomes from short-read resequencing data using breseq. BMC Genomics. 2014;15(1):1039. doi:10.1186/1471-2164-15-1039. PMID:25432719. PMCID:PMC4300727.
Afgan E, Baker D, van den Beek M, Blankenberg D, Bouvier D, Čech M, Chilton J, Clements D, Coraor N, Eberhard C, Grüning B, Guerler A, Hillman-Jackson J, Von Kuster G, Rasche E, Soranzo N, Turaga N, Taylor J, Nekrutenko A, Goecks J. The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2016 update. Nucleic Acids Research. 2016;44(W1):W3-W10. doi:10.1093/nar/gkw343. PMID:27137889. PMCID:PMC4987906.
Mareuil F, Doppelt-Azeroual O, Ménager H. A public Galaxy platform at Pasteur used as an execution engine for web services. Unknown Journal. 2017. doi:10.7490/f1000research.1114334.1.