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
Outputs
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.