Literature DB >> 22343431

Using probabilistic estimation of expression residuals (PEER) to obtain increased power and interpretability of gene expression analyses.

Oliver Stegle1, Leopold Parts, Matias Piipari, John Winn, Richard Durbin.   

Abstract

We present PEER (probabilistic estimation of expression residuals), a software package implementing statistical models that improve the sensitivity and interpretability of genetic associations in population-scale expression data. This approach builds on factor analysis methods that infer broad variance components in the measurements. PEER takes as input transcript profiles and covariates from a set of individuals, and then outputs hidden factors that explain much of the expression variability. Optionally, these factors can be interpreted as pathway or transcription factor activations by providing prior information about which genes are involved in the pathway or targeted by the factor. The inferred factors are used in genetic association analyses. First, they are treated as additional covariates, and are included in the model to increase detection power for mapping expression traits. Second, they are analyzed as phenotypes themselves to understand the causes of global expression variability. PEER extends previous related surrogate variable models and can be implemented within hours on a desktop computer.

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Mesh:

Year:  2012        PMID: 22343431      PMCID: PMC3398141          DOI: 10.1038/nprot.2011.457

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  33 in total

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Journal:  Nat Genet       Date:  2005-06-19       Impact factor: 38.330

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Journal:  Nat Genet       Date:  2006-07-09       Impact factor: 38.330

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  338 in total

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3.  A Burden of Rare Variants Associated with Extremes of Gene Expression in Human Peripheral Blood.

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4.  RNA Sequencing and Analysis.

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Journal:  Hum Mol Genet       Date:  2019-05-15       Impact factor: 6.150

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Journal:  JCI Insight       Date:  2016-09-08

7.  Prostate cancer risk SNP rs10993994 is a trans-eQTL for SNHG11 mediated through MSMB.

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8.  Gene expression elucidates functional impact of polygenic risk for schizophrenia.

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Journal:  Nat Neurosci       Date:  2016-09-26       Impact factor: 24.884

9.  Identification of a Core Module for Bone Mineral Density through the Integration of a Co-expression Network and GWAS Data.

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10.  A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease.

Authors:  Lasse Pihlstrøm; Cornelis Blauwendraat; Chiara Cappelletti; Victoria Berge-Seidl; Margrete Langmyhr; Sandra Pilar Henriksen; Wilma D J van de Berg; J Raphael Gibbs; Mark R Cookson; Andrew B Singleton; Mike A Nalls; Mathias Toft
Journal:  Ann Neurol       Date:  2018-08-26       Impact factor: 10.422

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