Bayesian mixture models for assessment of gene differential behaviour and prediction of pCR through the integration of copy number and gene expression data.

We consider modeling jointly microarray RNA expression and DNA copy number data. We propose Bayesian mixture models that define latent Gaussian probit scores for the DNA and RNA, and integrate between the two platforms via a regression of the RNA probit scores on the DNA probit scores. Such a regres...

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Main Authors: Filippo Trentini, Yuan Ji, Takayuki Iwamoto, Yuan Qi, Lajos Pusztai, Peter Müller
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3709899?pdf=render
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spelling doaj-e7a9d30637374f43822c18104ca853772020-11-25T02:15:26ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0187e6807110.1371/journal.pone.0068071Bayesian mixture models for assessment of gene differential behaviour and prediction of pCR through the integration of copy number and gene expression data.Filippo TrentiniYuan JiTakayuki IwamotoYuan QiLajos PusztaiPeter MüllerWe consider modeling jointly microarray RNA expression and DNA copy number data. We propose Bayesian mixture models that define latent Gaussian probit scores for the DNA and RNA, and integrate between the two platforms via a regression of the RNA probit scores on the DNA probit scores. Such a regression conveniently allows us to include additional sample specific covariates such as biological conditions and clinical outcomes. The two developed methods are aimed respectively to make inference on differential behaviour of genes in patients showing different subtypes of breast cancer and to predict the pathological complete response (pCR) of patients borrowing strength across the genomic platforms. Posterior inference is carried out via MCMC simulations. We demonstrate the proposed methodology using a published data set consisting of 121 breast cancer patients.http://europepmc.org/articles/PMC3709899?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Filippo Trentini
Yuan Ji
Takayuki Iwamoto
Yuan Qi
Lajos Pusztai
Peter Müller
spellingShingle Filippo Trentini
Yuan Ji
Takayuki Iwamoto
Yuan Qi
Lajos Pusztai
Peter Müller
Bayesian mixture models for assessment of gene differential behaviour and prediction of pCR through the integration of copy number and gene expression data.
PLoS ONE
author_facet Filippo Trentini
Yuan Ji
Takayuki Iwamoto
Yuan Qi
Lajos Pusztai
Peter Müller
author_sort Filippo Trentini
title Bayesian mixture models for assessment of gene differential behaviour and prediction of pCR through the integration of copy number and gene expression data.
title_short Bayesian mixture models for assessment of gene differential behaviour and prediction of pCR through the integration of copy number and gene expression data.
title_full Bayesian mixture models for assessment of gene differential behaviour and prediction of pCR through the integration of copy number and gene expression data.
title_fullStr Bayesian mixture models for assessment of gene differential behaviour and prediction of pCR through the integration of copy number and gene expression data.
title_full_unstemmed Bayesian mixture models for assessment of gene differential behaviour and prediction of pCR through the integration of copy number and gene expression data.
title_sort bayesian mixture models for assessment of gene differential behaviour and prediction of pcr through the integration of copy number and gene expression data.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description We consider modeling jointly microarray RNA expression and DNA copy number data. We propose Bayesian mixture models that define latent Gaussian probit scores for the DNA and RNA, and integrate between the two platforms via a regression of the RNA probit scores on the DNA probit scores. Such a regression conveniently allows us to include additional sample specific covariates such as biological conditions and clinical outcomes. The two developed methods are aimed respectively to make inference on differential behaviour of genes in patients showing different subtypes of breast cancer and to predict the pathological complete response (pCR) of patients borrowing strength across the genomic platforms. Posterior inference is carried out via MCMC simulations. We demonstrate the proposed methodology using a published data set consisting of 121 breast cancer patients.
url http://europepmc.org/articles/PMC3709899?pdf=render
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