TSVdb: a web-tool for TCGA splicing variants analysis

BMC Genomics. 2018 May 29;19(1):405. doi: 10.1186/s12864-018-4775-x.

Abstract

Background: Collaborative projects such as The Cancer Genome Atlas (TCGA) have generated various -omics and clinical data on cancer. Many computational tools have been developed to facilitate the study of the molecular characterization of tumors using data from the TCGA. Alternative splicing of a gene produces splicing variants, and accumulating evidence has revealed its essential role in cancer-related processes, implying the urgent need to discover tumor-specific isoforms and uncover their potential functions in tumorigenesis.

Result: We developed TSVdb, a web-based tool, to explore alternative splicing based on TCGA samples with 30 clinical variables from 33 tumors. TSVdb has an integrated and well-proportioned interface for visualization of the clinical data, gene expression, usage of exons/junctions and splicing patterns. Researchers can interpret the isoform expression variations between or across clinical subgroups and estimate the relationships between isoforms and patient prognosis. TSVdb is available at http://www.tsvdb.com , and the source code is available at https://github.com/wenjie1991/TSVdb .

Conclusion: TSVdb will inspire oncologists and accelerate isoform-level advances in cancer research.

Keywords: Alternative splicing; Cancer; Splicing variant; TCGA; Visualization tools.

MeSH terms

  • Colonic Neoplasms / genetics
  • Genomics / methods*
  • Internet*
  • Neoplasms / genetics*
  • RNA Splicing*