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Published April 3, 2017 | Version v1
Dataset Open

Alternative splicing changes as drivers of cancer

Creators

  • 1. Institut Curie
  • 2. Sanford Burnham Prebys Medical Discovery Institute
  • 3. Catalan Institution of Research and Advanced Studies

Description

This dataset contains information on alternative splicing isoform switches as described in the related paper "Alternative splicing changes as drivers of cancer" (pre-print available). It contains the list of the observed switches, altogether with their functional implications (effect on the protein, on the PPI network, etc.) and related measures of relevance (links to mutational data, etc.). This dataset was thoroughly explored in a related Jupyter notebook.

Notes

HCG and EE were supported by the MINECO and FEDER (BIO2014-52566-R), Consolider RNAREG (CSD2009-00080), AGAUR (SGR2014-1121), and the Sandra Ibarra Foundation for Cancer (FSI2013). EPP and AG were supported by the SBP CC grant (P30 CA030199). All authors thank The Cancer Genome Atlas project for making their results publicly available for further analysis.

Files

smartas_data.zip

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Additional details

Related works

Is cited by
10.1101/076653 (DOI)
Is compiled by
https://bitbucket.org/regulatorygenomicsupf/smartas/src (URL)
Is supplement to
https://github.com/hclimente/smartas (URL)