Evidence map›Paper›PMID 32723302›Full record

ArticleBMC genomics2020

Multi-trait multi-locus SEM model discriminates SNPs of different effects.

Anna A Igolkina, Georgy Meshcheryakov, Maria V Gretsova, Sergey V Nuzhdin, Maria G Samsonova

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Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Anna A IgolkinaPeter the Great Saint-Petersburg Polytechnic University, Russian Federation, Polytechnicheskaya, 29, St. Petersburg, 195251, Russia. igolkinaanna11@gmail.com.ORCID http://orcid.org/0000-0001-8851-9621
Georgy MeshcheryakovPeter the Great Saint-Petersburg Polytechnic University, Russian Federation, Polytechnicheskaya, 29, St. Petersburg, 195251, Russia.
Maria V GretsovaPeter the Great Saint-Petersburg Polytechnic University, Russian Federation, Polytechnicheskaya, 29, St. Petersburg, 195251, Russia.
Sergey V NuzhdinPeter the Great Saint-Petersburg Polytechnic University, Russian Federation, Polytechnicheskaya, 29, St. Petersburg, 195251, Russia.
Maria G SamsonovaPeter the Great Saint-Petersburg Polytechnic University, Russian Federation, Polytechnicheskaya, 29, St. Petersburg, 195251, Russia. msamsonova@spbstu.ru.

Funding

RFBR 18‒29‒13033
6 · The paper itself

Abstract

backgroundThere is a plethora of methods for genome-wide association studies. However, only a few of them may be classified as multi-trait and multi-locus, i.e. consider the influence of multiple genetic variants to several correlated phenotypes.

resultsWe propose a multi-trait multi-locus model which employs structural equation modeling (SEM) to describe complex associations between SNPs and traits - multi-trait multi-locus SEM (mtmlSEM). The structure of our model makes it possible to discriminate pleiotropic and single-trait SNPs of direct and indirect effect. We also propose an automatic procedure to construct the model using factor analysis and the maximum likelihood method. For estimating a large number of parameters in the model, we performed Bayesian inference and implemented Gibbs sampling. An important feature of the model is that it correctly copes with non-normally distributed variables, such as some traits and variants.

conclusionsWe applied the model to Vavilov's collection of 404 chickpea (Cicer arietinum L.) accessions with 20-fold cross-validation. We analyzed 16 phenotypic traits which we organized into five groups and found around 230 SNPs associated with traits, 60 of which were of pleiotropic effect. The model demonstrated high accuracy in predicting trait values.

Indexed as

Latent Class AnalysisBayes TheoremGenome-Wide Association StudyGenotypeHumansLikelihood FunctionsPolymorphism, Single NucleotideQuantitative Trait LociBayesian inferenceChickpeaGWASMulti-trait multi-locus SEMSEM

Identifiers

PMID32723302
PMCPMC7385891

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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.