Evidence map›Paper›PMID 33369784›Full record

ArticleGenetic epidemiology2021

Multi-tissue transcriptome-wide association studies.

Nastasiya F Grinberg, Chris Wallace

Abstract read
In one paragraph

Article in Genetic epidemiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–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

14 citing papers in PubMed.

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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

2 authors.

Nastasiya F GrinbergDepartment of Medicine, Jeffrey Cheah Biomedical Centre, Cambridge Biomedical Campus, Cambridge Institute of Therapeutic Immunology and Infectious Disease, University of Cambridge, Cambridge, UK.ORCID 0000-0002-2727-5130
Chris WallaceDepartment of Medicine, Jeffrey Cheah Biomedical Centre, Cambridge Biomedical Campus, Cambridge Institute of Therapeutic Immunology and Infectious Disease, University of Cambridge, Cambridge, UK.ORCID 0000-0001-9755-1703

Funding

Medical Research Council MC_UU_00002/4Wellcome Trust WT107881
6 · The paper itself

Abstract

A transcriptome-wide association study (TWAS) attempts to identify disease associated genes by imputing gene expression into a genome-wide association study (GWAS) using an expression quantitative trait loci (eQTL) data set and then testing for associations with a trait of interest. Regulatory processes may be shared across related tissues and one natural extension of TWAS is harnessing cross-tissue correlation in gene expression to improve prediction accuracy. Here, we studied multi-tissue extensions of lasso regression and random forests (RF), joint lasso and RF-MTL (multi-task learning RF), respectively. We found that, on our chosen eQTL data set, multi-tissue methods were generally more accurate than their single-tissue counterparts, with RF-MTL performing the best. Simulations showed that these benefits generally translated into more associated genes identified, although highlighted that joint lasso had a tendency to erroneously identify genes in one tissue if there existed an eQTL signal for that gene in another. Applying the four methods to a type 1 diabetes GWAS, we found that multi-tissue methods found more unique associated genes for most of the tissues considered. We conclude that multi-tissue methods are competitive and, for some cell types, superior to single-tissue approaches and hold much promise for TWAS studies.

Indexed as

Genome-Wide Association StudyTranscriptomeHumansModels, GeneticPhenotypeQuantitative Trait Locicomplex traitsgene expressionmulti-task learningtranscriptome-wide association studies

Identifiers

PMID33369784
PMCPMC8048510

What Socratic holds

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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 Socratic graph.