Evidence map›Paper›PMID 26504141›Full record

ArticleBioinformatics (Oxford, England)2016

MT-HESS: an efficient Bayesian approach for simultaneous association detection in OMICS datasets, with application to eQTL mapping in multiple tissues.

Alex Lewin, Habib Saadi, James E Peters, Aida Moreno-Moral, James C Lee, Kenneth G C Smith, Enrico Petretto, Leonardo Bottolo, Sylvia Richardson

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

15 citing papers in PubMed.

  1. Article
  2. fSuSiE enables fine-mapping of QTLs from genome-scale molecular profiles.bioRxiv : the preprint server for biology · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Expression Quantitative Trait Loci Analysis in Multiple Tissues.Methods in molecular biology (Clifton, N.J.) · 2020
    Article
  8. Article
  9. Article
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  11. Article
  12. Review
  13. Article
  14. Bayesian Variable Selection Methods for Matched Case-Control Studies.The international journal of biostatistics · 2017
    Article
  15. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Alex LewinDepartment of Mathematics, Brunel University London.
Habib SaadiDepartment of Epidemiology and Biostatistics, Imperial College London, London.
James E PetersCambridge Institute for Medical Research, University of Cambridge, Cambridge, MRC Biostatistics Unit, Cambridge Institute of Public Health, Cambridge.
Aida Moreno-MoralMRC Clinical Sciences Centre, Imperial College London, London, UK.
James C LeeCambridge Institute for Medical Research, University of Cambridge, Cambridge.
Kenneth G C SmithCambridge Institute for Medical Research, University of Cambridge, Cambridge.
Enrico PetrettoMRC Clinical Sciences Centre, Imperial College London, London, UK, Duke-NUS Graduate Medical School, Singapore, Singapore.
Leonardo BottoloDepartment of Mathematics, Imperial College London, London, UK and Department of Medical Genetics, University of Cambridge.
Sylvia RichardsonMRC Biostatistics Unit, Cambridge Institute of Public Health, Cambridge.

Funding

British Heart Foundation FS/11/25/28740Medical Research Council G1002319Medical Research Council MC_U120097112Medical Research Council MC_UP_0801/1Medical Research Council MR/L19027/1Medical Research Council MR/M013138/1Wellcome Trust 083650/Z/07/ZWellcome Trust 100140
6 · The paper itself

Abstract

motivationAnalysing the joint association between a large set of responses and predictors is a fundamental statistical task in integrative genomics, exemplified by numerous expression Quantitative Trait Loci (eQTL) studies. Of particular interest are the so-called ': hotspots ': , important genetic variants that regulate the expression of many genes. Recently, attention has focussed on whether eQTLs are common to several tissues, cell-types or, more generally, conditions or whether they are specific to a particular condition.

resultsWe have implemented MT-HESS, a Bayesian hierarchical model that analyses the association between a large set of predictors, e.g. SNPs, and many responses, e.g. gene expression, in multiple tissues, cells or conditions. Our Bayesian sparse regression algorithm goes beyond ': one-at-a-time ': association tests between SNPs and responses and uses a fully multivariate model search across all linear combinations of SNPs, coupled with a model of the correlation between condition/tissue-specific responses. In addition, we use a hierarchical structure to leverage shared information across different genes, thus improving the detection of hotspots. We show the increase of power resulting from our new approach in an extensive simulation study. Our analysis of two case studies highlights new hotspots that would remain undetected by standard approaches and shows how greater prediction power can be achieved when several tissues are jointly considered. AVAILABILITY AND IMPLEMENTATION: C[Formula: see text] source code and documentation including compilation instructions are available under GNU licence at http://www.mrc-bsu.cam.ac.uk/software/.

Indexed as

AlgorithmsBayes TheoremGene Expression RegulationGene Regulatory NetworksSoftwareAnimalsDiabetes Mellitus, Type 1GenomicsHumansInflammationInflammatory Bowel DiseasesModels, TheoreticalOrgan SpecificityPolymorphism, Single NucleotideProgramming LanguagesQuantitative Trait Loci

Identifiers

PMID26504141
PMCPMC4743623

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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.