Evidence map›Paper›PMID 20386736›Full record

ArticlePLoS computational biology2010

New insights into the genetic control of gene expression using a Bayesian multi-tissue approach.

Enrico Petretto, Leonardo Bottolo, Sarah R Langley, Matthias Heinig, Chris McDermott-Roe, Rizwan Sarwar, Michal Pravenec, Norbert Hübner, Timothy J Aitman, Stuart A Cook and 1 more

Abstract read
In one paragraph

Article in PLoS computational biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  16. HDTD: analyzing multi-tissue gene expression data.Bioinformatics (Oxford, England) · 2016
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Enrico PetrettoMedical Research Council Clinical Sciences Centre, Faculty of Medicine, Imperial College London, London, United Kingdom.
Leonardo Bottolo
Sarah R Langley
Matthias Heinig
Chris McDermott-Roe
Rizwan Sarwar
Michal Pravenec
Norbert Hübner
Timothy J Aitman
Stuart A Cook
Sylvia Richardson

Funding

Biotechnology and Biological Sciences Research Council BB/C519670/1British Heart FoundationMedical Research Council G0600609Medical Research Council MC_U120061454Medical Research Council MC_U120085815Medical Research Council MC_U120097112Wellcome TrustWellcome Trust P14515
6 · The paper itself

Abstract

The majority of expression quantitative trait locus (eQTL) studies have been carried out in single tissues or cell types, using methods that ignore information shared across tissues. Although global analysis of RNA expression in multiple tissues is now feasible, few integrated statistical frameworks for joint analysis of gene expression across tissues combined with simultaneous analysis of multiple genetic variants have been developed to date. Here, we propose Sparse Bayesian Regression models for mapping eQTLs within individual tissues and simultaneously across tissues. Testing these on a set of 2,000 genes in four tissues, we demonstrate that our methods are more powerful than traditional approaches in revealing the true complexity of the eQTL landscape at the systems-level. Highlighting the power of our method, we identified a two-eQTL model (cis/trans) for the Hopx gene that was experimentally validated and was not detected by conventional approaches. We showed common genetic regulation of gene expression across four tissues for approximately 27% of transcripts, providing >5 fold increase in eQTLs detection when compared with single tissue analyses at 5% FDR level. These findings provide a new opportunity to uncover complex genetic regulatory mechanisms controlling global gene expression while the generality of our modelling approach makes it adaptable to other model systems and humans, with broad application to analysis of multiple intermediate and whole-body phenotypes.

Indexed as

Bayes TheoremModels, GeneticQuantitative Trait LociAdipose TissueAdrenal GlandsAlgorithmsAnimalsGene Expression ProfilingGene Expression RegulationGene Regulatory NetworksHeart VentriclesHumansKidneyRegression AnalysisReproducibility of ResultsSensitivity and Specificity

Identifiers

PMID20386736
PMCPMC2851562

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.