rgpicfixmate

rgpicfixmate synchronizes mate-pair information between paired-end sequencing reads to ensure consistent read-pair metadata for downstream analyses such as genome assembly, structural variant detection, and transcriptome analysis.


Key Features:

  • Mate-Pair Synchronization: Ensures mate-pair information is consistent and aligned between each read and its corresponding mate.
  • Integration with Galaxy Project: Operates within the Galaxy framework to integrate with Galaxy workflows and data histories.
  • Reproducibility and Transparency: Leverages Galaxy's tracking of computational steps to support reproducible analyses.

Scientific Applications:

  • Genome Assembly: Improves accuracy and contiguity of genome assemblies by providing consistent mate-pair information.
  • Structural Variant Detection: Facilitates identification of structural variants by ensuring reliable read-pair orientations and pairing relationships.
  • Transcriptome Analysis: Enhances detection of transcript isoforms and alternative splicing by maintaining correct paired-end relationships.

Methodology:

Operates within the Galaxy framework; paired-end sequencing reads are provided into Galaxy, rgpicfixmate processes those reads to synchronize mate-pair information, and the synchronized read output is made available within Galaxy for downstream analysis.

Topics

Collections

Details

Maturity:
Mature
Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Programming Languages:
Java
Added:
12/19/2016
Last Updated:
11/25/2024

Operations

Data Inputs & Outputs

Sequence editing

Publications

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.

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.

Documentation

Links