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
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.