Evidence map›Paper›PMID 35442943›Full record

ArticlePLoS genetics2022

Efficient estimation of SNP heritability using Gaussian predictive process in large scale cohort studies.

Souvik Seal, Abhirup Datta, Saonli Basu

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In one paragraph

Article in PLoS genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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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

3 authors.

Souvik SealDepartment of Biostatistics and Informatics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.ORCID 0000-0003-3268-610X
Abhirup DattaDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.ORCID 0000-0002-5046-0289
Saonli BasuDepartment of Biostatistics, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID 0000-0003-1200-4546

Funding

Statistical Methods for detection of genome-wide GxE interactions in longitudinalR01DA033958 · NIDA · UNIVERSITY OF MINNESOTA · PI BASU, SAONLI · 2013 to 2016
$1.1M
Improved Heritability Estimation by Spatial Mapping of Genetic RelationshipsR21DA046188 · NIDA · UNIVERSITY OF MINNESOTA · PI BASU, SAONLI · 2018 to 2019
$398k
Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NIDA NIH HHS R01 DA033958NIDA NIH HHS R21 DA046188
6 · The paper itself

Abstract

With the advent of high throughput genetic data, there have been attempts to estimate heritability from genome-wide SNP data on a cohort of distantly related individuals using linear mixed model (LMM). Fitting such an LMM in a large scale cohort study, however, is tremendously challenging due to its high dimensional linear algebraic operations. In this paper, we propose a new method named PredLMM approximating the aforementioned LMM motivated by the concepts of genetic coalescence and Gaussian predictive process. PredLMM has substantially better computational complexity than most of the existing LMM based methods and thus, provides a fast alternative for estimating heritability in large scale cohort studies. Theoretically, we show that under a model of genetic coalescence, the limiting form of our approximation is the celebrated predictive process approximation of large Gaussian process likelihoods that has well-established accuracy standards. We illustrate our approach with extensive simulation studies and use it to estimate the heritability of multiple quantitative traits from the UK Biobank cohort.

Indexed as

Genome-Wide Association StudyModels, GeneticCohort StudiesHumansLinear ModelsNormal DistributionPhenotypePolymorphism, Single Nucleotide

Identifiers

PMID35442943
PMCPMC9060362

What Socratic holds

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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.