DoChaP

DoChaP visualizes exon-domain associations to reveal how alternative splicing alters protein domain composition across transcripts and between species.


Key Features:

  • Exon-domain visualization: Visualizes exon-domain associations across all transcripts of a gene, mapping exons to protein domains.
  • Protein-domain mapping: Displays encoded protein isoforms and their annotated domains to enable direct comparison between transcripts and protein products.
  • Color-coded comparative visualization: Uses color-coded, organized displays to highlight structural changes in protein architecture resulting from alternative splicing.
  • Two-species comparison: Performs pairwise exon-domain comparisons between two species to assess conservation of exons, splicing events, and domain architecture.
  • Automated analysis across genes: Automates integration of exon and domain data to support multi-gene and scalable analyses that reduce manual integration efforts.

Scientific Applications:

  • Alternative splicing impact analysis: Assess how alternative splicing modifies protein domain composition and isoform architecture.
  • Evolutionary conservation studies: Investigate conservation of exons, splicing patterns, and domain arrangements between species.
  • Structural consequence evaluation: Examine structural changes in protein architecture caused by splicing variants relevant to health and disease.
  • Genomic-scale splicing studies: Support genomic investigations linking alternative splicing events to changes in protein domain organization.

Methodology:

Visualizes exon-domain associations across transcripts, displays encoded proteins with annotated domains, and performs comparative exon-domain analysis between two species.

Topics

Details

License:
MIT
Tool Type:
web application
Programming Languages:
JavaScript, Python
Added:
9/8/2021
Last Updated:
9/13/2021

Operations

Publications

Gal-Oz ST, Haiat N, Eliyahu D, Shani G, Shay T. DoChaP: the domain change presenter. Nucleic Acids Research. 2021;49(W1):W162-W168. doi:10.1093/nar/gkab357. PMID:33988713. PMCID:PMC8262731.

PMID: 33988713
Funding: - Israel Science Foundation: 1210/18, 500/15 - National Institutes of Health: R24AI072073

Links