G-OnRamp

G-OnRamp facilitates collaborative eukaryotic genome annotation by integrating evidence tracks from sequence alignments, ab initio gene predictors, RNA-Seq data, and repeat finders for visualization in UCSC Assembly Hubs and JBrowse/Apollo genome browsers.


Key Features:

  • End-to-end annotation: Supports the full genome annotation workflow from input data processing to annotation output.
  • Evidence track integration: Integrates sequence alignments, ab initio gene predictors, RNA-Seq-derived evidence, and repeat finder results into composite evidence tracks.
  • Genome browser visualization: Generates UCSC Assembly Hubs and configures JBrowse/Apollo genome browsers to display evidence tracks.
  • Collaborative annotation: Supports collaborative curation of gene models via Apollo, allowing multiple users to contribute to shared annotations.

Scientific Applications:

  • Collaborative genome annotation projects: Supports eukaryotic genome annotation projects that require integrating multiple evidence types across contributors.
  • Gene structure prediction: Facilitates prediction and refinement of gene models by combining sequence alignments, ab initio predictions, and RNA-Seq evidence.
  • Educational genomics: Enables hands-on annotation exercises for teaching genomics and bioinformatics using real datasets.

Methodology:

Generates evidence tracks from sequence alignments, ab initio gene prediction, RNA-Seq data analysis, and repeat detection, and visualizes them using JBrowse/Apollo and UCSC Assembly Hubs.

Topics

Details

License:
Unlicense
Maturity:
Mature
Cost:
Free of charge
Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Added:
8/9/2019
Last Updated:
11/24/2024

Operations

Publications

Liu Y, Sargent L, Leung W, Elgin SCR, Goecks J. G-OnRamp: a Galaxy-based platform for collaborative annotation of eukaryotic genomes. Bioinformatics. 2019;35(21):4422-4423. doi:10.1093/bioinformatics/btz309. PMID:31070714. PMCID:PMC6821377.

PMID: 31070714
PMCID: PMC6821377
Funding: - National Institutes of Health: 1R25 GM119157

Documentation