CoINcIDE: A framework for discovery of patient subtypes across multiple datasets.

Genome Med

The Stanford Center for Biomedical Informatics Research (BMIR), Department of Medicine, Stanford University, 1265 Welch Road, Stanford, CA, 94305, USA.

Published: March 2016

Patient disease subtypes have the potential to transform personalized medicine. However, many patient subtypes derived from unsupervised clustering analyses on high-dimensional datasets are not replicable across multiple datasets, limiting their clinical utility. We present CoINcIDE, a novel methodological framework for the discovery of patient subtypes across multiple datasets that requires no between-dataset transformations. We also present a high-quality database collection, curatedBreastData, with over 2,500 breast cancer gene expression samples. We use CoINcIDE to discover novel breast and ovarian cancer subtypes with prognostic significance and novel hypothesized ovarian therapeutic targets across multiple datasets. CoINcIDE and curatedBreastData are available as R packages.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4784276PMC
http://dx.doi.org/10.1186/s13073-016-0281-4DOI Listing

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