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dc.contributor.authorMalik, Muhammad Ammar
dc.contributor.authorMichoel, Tom
dc.date.accessioned2022-08-11T06:51:40Z
dc.date.available2022-08-11T06:51:40Z
dc.date.created2022-05-19T10:34:27Z
dc.date.issued2022
dc.identifier.issn2160-1836
dc.identifier.urihttps://hdl.handle.net/11250/3011196
dc.description.abstractRandom effects models are popular statistical models for detecting and correcting spurious sample correlations due to hidden confounders in genome-wide gene expression data. In applications where some confounding factors are known, estimating simultaneously the contribution of known and latent variance components in random effects models is a challenge that has so far relied on numerical gradient-based optimizers to maximize the likelihood function. This is unsatisfactory because the resulting solution is poorly characterized and the efficiency of the method may be suboptimal. Here, we prove analytically that maximum-likelihood latent variables can always be chosen orthogonal to the known confounding factors, in other words, that maximum-likelihood latent variables explain sample covariances not already explained by known factors. Based on this result, we propose a restricted maximum-likelihood (REML) method that estimates the latent variables by maximizing the likelihood on the restricted subspace orthogonal to the known confounding factors and show that this reduces to probabilistic principal component analysis on that subspace. The method then estimates the variance–covariance parameters by maximizing the remaining terms in the likelihood function given the latent variables, using a newly derived analytic solution for this problem. Compared to gradient-based optimizers, our method attains greater or equal likelihood values, can be computed using standard matrix operations, results in latent factors that do not overlap with any known factors, and has a runtime reduced by several orders of magnitude. Hence, the REML method facilitates the application of random effects modeling strategies for learning latent variance components to much larger gene expression datasets than possible with current methods.en_US
dc.language.isoengen_US
dc.publisherOxford University Pressen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleRestricted maximum-likelihood method for learning latent variance components in gene expression data with known and unknown confoundersen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2021 the authorsen_US
dc.source.articlenumberjkab410en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.doi10.1093/g3journal/jkab410
dc.identifier.cristin2025498
dc.source.journalG3: Genes, Genomes, Geneticsen_US
dc.identifier.citationG3: Genes, Genomes, Genetics. 2022, 12 (2), jkab410.en_US
dc.source.volume12en_US
dc.source.issue2en_US


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