Evidence map›Paper›PMID 27479908›Full record

ArticleNature genetics2016

Tensor decomposition for multiple-tissue gene expression experiments.

Victoria Hore, Ana Viñuela, Alfonso Buil, Julian Knight, Mark I McCarthy, Kerrin Small, Jonathan Marchini

Open access · greenAbstract read
In one paragraph

Article in Nature genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 2 pooled it
20.7field-weighted citation impact, top 1% of its field
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

70 citing papers in PubMed, 2 syntheses or guidelines pooled it, 205 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. BAMITA: Bayesian multiple imputation for tensor arrays.Biostatistics (Oxford, England) · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Probabilistic PARAFAC2.Entropy (Basel, Switzerland) · 2024
    Article
  20. Review

10 more citing papers are in PubMed but not listed here.

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

7 authors at 4 institutions in 2 countries.

Victoria HoreDepartment of Statistics, University of Oxford, Oxford, UK.
Ana ViñuelaDepartment of Twin Research and Genetic Epidemiology, King's College London, London, UK.
Alfonso BuilDepartment of Genetic Medicine and Development, University of Geneva, Geneva, Switzerland.
Julian KnightWellcome Trust Centre for Human Genetics, Oxford, UK.
Mark I McCarthyWellcome Trust Centre for Human Genetics, Oxford, UK.
Kerrin SmallDepartment of Twin Research and Genetic Epidemiology, King's College London, London, UK.ORCID 0000-0003-4566-0005
Jonathan MarchiniDepartment of Statistics, University of Oxford, Oxford, UK.ORCID 0000-0003-0610-8322
Centre for Human Genetics · GBKing's College London · GBUniversity of Geneva · CHUniversity of Oxford · GB

Funding

European Research Council 617306Medical Research Council MR/L01999X/1Wellcome Trust
6 · The paper itself

Abstract

Genome-wide association studies of gene expression traits and other cellular phenotypes have successfully identified links between genetic variation and biological processes. The majority of discoveries have uncovered cis-expression quantitative trait locus (eQTL) effects via mass univariate testing of SNPs against gene expression in single tissues. Here we present a Bayesian method for multiple-tissue experiments focusing on uncovering gene networks linked to genetic variation. Our method decomposes the 3D array (or tensor) of gene expression measurements into a set of latent components. We identify sparse gene networks that can then be tested for association against genetic variation across the genome. We apply our method to a data set of 845 individuals from the TwinsUK cohort with gene expression measured via RNA-seq analysis in adipose, lymphoblastoid cell lines (LCLs) and skin. We uncover several gene networks with a genetic basis and clear biological and statistical significance. Extensions of this approach will allow integration of different omics, environmental and phenotypic data sets.

Indexed as

Bayes TheoremAdipose TissueCohort StudiesGene Expression ProfilingGene Expression RegulationGene Regulatory NetworksGenetic MarkersGenome-Wide Association StudyHumansLymphocytesPhenotypePolymorphism, Single NucleotideQuantitative Trait LociSkinUnited KingdomGenetic Markers

Identifiers

PMID27479908
PMCPMC5010142
OpenAlexW2482092413

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.