TSVdb: A web-tool for TCGA splicing variants analysis

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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.

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Sun, W., Duan, T., Ye, P., Chen, K., Zhang, G., Lai, M., & Zhang, H. (2018). TSVdb: A web-tool for TCGA splicing variants analysis. BMC Genomics, 19(1). https://doi.org/10.1186/s12864-018-4775-x

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