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Assessing reproducibility of matrix factorization methods in independent transcriptomes

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dc.contributor.author Cantini, Laura
dc.contributor.author Kairov, Ulykbek
dc.contributor.author de Reynies, Aurelien
dc.contributor.author Barillot, Emmanuel
dc.contributor.author Radvanyi, Francois
dc.contributor.author Zinovyev, Andrei
dc.date.accessioned 2019-12-11T09:30:18Z
dc.date.available 2019-12-11T09:30:18Z
dc.date.issued 2019
dc.identifier.citation Cantini, L., Kairov, U., de Reyniès, A., Barillot, E., Radvanyi, F., & Zinovyev, A. (2019). Assessing reproducibility of matrix factorization methods in independent transcriptomes. Bioinformatics, 35(21), 4307–4313. https://doi.org/10.1093/bioinformatics/btz225 en_US
dc.identifier.other 10.1093/bioinformatics/btz225
dc.identifier.uri http://nur.nu.edu.kz/handle/123456789/4391
dc.description https://www.ncbi.nlm.nih.gov/pubmed/30938767 en_US
dc.description.abstract Motivation Matrix factorization (MF) methods are widely used in order to reduce dimensionality of transcriptomic datasets to the action of few hidden factors (metagenes). MF algorithms have never been compared based on the between-datasets reproducibility of their outputs in similar independent datasets. Lack of this knowledge might have a crucial impact when generalizing the predictions made in a study to others. Results We systematically test widely used MF methods on several transcriptomic datasets collected from the same cancer type (14 colorectal, 8 breast and 4 ovarian cancer transcriptomic datasets). Inspired by concepts of evolutionary bioinformatics, we design a novel framework based on Reciprocally Best Hit (RBH) graphs in order to benchmark the MF methods for their ability to produce generalizable components. We show that a particular protocol of application of independent component analysis (ICA), accompanied by a stabilization procedure, leads to a significant increase in the between-datasets reproducibility. Moreover, we show that the signals detected through this method are systematically more interpretable than those of other standard methods. We developed a user-friendly tool for performing the Stabilized ICA-based RBH meta-analysis. We apply this methodology to the study of colorectal cancer (CRC) for which 14 independent transcriptomic datasets can be collected. The resulting RBH graph maps the landscape of interconnected factors associated to biological processes or to technological artifacts. These factors can be used as clinical biomarkers or robust and tumor-type specific transcriptomic signatures of tumoral cells or tumoral microenvironment. Their intensities in different samples shed light on the mechanistic basis of CRC molecular subtyping. Availability and implementation The RBH construction tool is available from http://goo.gl/DzpwYp Supplementary information Supplementary data are available at Bioinformatics online. en_US
dc.language.iso en en_US
dc.publisher OXFORD UNIV PRESS en_US
dc.rights Attribution-NonCommercial-ShareAlike 3.0 United States *
dc.rights.uri http://creativecommons.org/licenses/by-nc-sa/3.0/us/ *
dc.subject Assessing reproducibility en_US
dc.subject Gene expression en_US
dc.subject Matrix factorization en_US
dc.subject MF en_US
dc.subject colorectal cancer en_US
dc.subject CRC en_US
dc.subject breast cancer en_US
dc.subject BRCA en_US
dc.title Assessing reproducibility of matrix factorization methods in independent transcriptomes en_US
dc.type Article en_US
workflow.import.source science


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