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

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.

Documentation

Links