gdtools_not-evidence

gdtools_not-evidence filters GenomeDiff files to remove entries that are not used as evidence for mutations, producing a refined GenomeDiff focused on mutation-supporting records.


Key Features:

  • Selective Filtering: Identifies and removes GenomeDiff entries that are not utilized as evidence for mutations.
  • Output Customization: Writes the refined GenomeDiff to a specified output path or, if none is provided, emits a verbose report listing excluded entries.
  • Integration with Galaxy Platform: Executes within the Galaxy platform as a Galaxy tool, enabling execution in Galaxy-managed workflows and on compute resources such as clusters at Institut Pasteur.
  • Web Service Compatibility: Interacts with Galaxy via the Galaxy API or the Bioblend library to submit and manage computational tasks.

Scientific Applications:

  • Genomic Research: Refines GenomeDiff files to focus analyses on mutation evidence for studies of genetic variation, disease association, and evolutionary biology.
  • Data Management: Reduces non-contributory entries in GenomeDiff datasets to decrease storage and downstream computational load.

Methodology:

Parses GenomeDiff files to identify and remove entries that do not contribute to mutation evidence; runs as an automated Galaxy job and can provide verbose output when no explicit output path is specified; communicates with Galaxy via the Galaxy API or Bioblend.

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

Editing

Inputs

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.

Documentation

Links