The trait coding rule in phenotype space

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This study developed a dimension decomposition method to separate genetically determined (PG) and non-genetically determined (PNG) trait subspaces, finding that PG uses a small set of recurrent dimensions while PNG uses numerous trait-specific dimensions.

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The preprint studies how to infer genetically determined values of quantitative traits by decomposing phenotype space into a genetic subspace (PG) and a non-genetic subspace (PNG), motivated by the idea that PG uses limited dimensions while PNG can involve many. After validating a dimension decomposition method with simulations, the authors apply it to yeast using 405 traits and report that the inferred PG matches known genetic components, explains broad-sense heritability, and supports quantitative trait locus mapping, while PG uses a small set of recurrent latent dimensions and PNG dimensions are more trait-specific and increase with trait sampling. They further analyze UK Biobank human brain phenome data and use the same framework to characterize genetic versus non-genetic origins of left-right asymmetry. A key limitation explicitly reflected in the preprint framing is that it is not peer reviewed. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

Abstract Is it possible to infer the genetically determined value of a quantitative trait from other traits? To answer the question we need to know how traits are coded in phenotype space (P) which can be partitioned into a subspace determined by genetic factors (PG) and a subspace affected by non-genetic factors (PNG). Evolutionary theory predicts PG is composed of limited dimensions while PNG may have infinite dimensions, which suggests a novel dimension decomposition method to separate them. After validating the method using simulation we applied it to a yeast phenotype space comprising 405 traits. The obtained yeast PG matches the actual genetic components of the yeast traits, explains the broad-sense heritability, and facilitates the mapping of quantitative trait loci, highlighting the success of the subspace separation. A limited number of latent dimensions in the PG were found to be recurrently used for coding the diverse yeast traits, while dimensions in the PNG tend to be trait specific and increase constantly with trait sampling. Similar results were obtained by analyzing the UK Biobank human brain phenome, which elucidated the genetic versus non-genetic origins of the left-right asymmetry of brain. In sum, phenotypic traits are coded by a rather small set of genetically determined basic dimensions and numerous trait-specific dimensions that are shaped by non-genetic factors, a rule enabling the identification of genetic components of quantitative traits based solely on phenotype.
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The trait coding rule in phenotype space | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Article The trait coding rule in phenotype space Jianguo Wang, Xionglei He This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-1297947/v1 This work is licensed under a CC BY 4.0 License Status: Posted Version 1 posted You are reading this latest preprint version Abstract Is it possible to infer the genetically determined value of a quantitative trait from other traits? To answer the question we need to know how traits are coded in phenotype space (P) which can be partitioned into a subspace determined by genetic factors (PG) and a subspace affected by non-genetic factors (PNG). Evolutionary theory predicts PG is composed of limited dimensions while PNG may have infinite dimensions, which suggests a novel dimension decomposition method to separate them. After validating the method using simulation we applied it to a yeast phenotype space comprising 405 traits. The obtained yeast PG matches the actual genetic components of the yeast traits, explains the broad-sense heritability, and facilitates the mapping of quantitative trait loci, highlighting the success of the subspace separation. A limited number of latent dimensions in the PG were found to be recurrently used for coding the diverse yeast traits, while dimensions in the PNG tend to be trait specific and increase constantly with trait sampling. Similar results were obtained by analyzing the UK Biobank human brain phenome, which elucidated the genetic versus non-genetic origins of the left-right asymmetry of brain. In sum, phenotypic traits are coded by a rather small set of genetically determined basic dimensions and numerous trait-specific dimensions that are shaped by non-genetic factors, a rule enabling the identification of genetic components of quantitative traits based solely on phenotype. Full Text Additional Declarations There is NO Competing Interest. Supplementary Files rs.pdf Reporting Summary Cite Share Download PDF Status: Posted Version 1 posted You are reading this latest preprint version Research Square lets you share your work early, gain feedback from the community, and start making changes to your manuscript prior to peer review in a journal. As a division of Research Square Company, we’re committed to making research communication faster, fairer, and more useful. We do this by developing innovative software and high quality services for the global research community. Our growing team is made up of researchers and industry professionals working together to solve the most critical problems facing scientific publishing. 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