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Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals

Attributing the similarity between individuals to genetic and non-genetic factors is central to genetic analyses. In this paper we use the genomic relationship ([Formula: see text] ) among 417,060 individuals to investigate the phenotypic covariance between pairs of individuals for 32 traits across...

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Autores principales: Kemper, Kathryn E., Yengo, Loic, Zheng, Zhili, Abdellaoui, Abdel, Keller, Matthew C., Goddard, Michael E., Wray, Naomi R., Yang, Jian, Visscher, Peter M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886899/
https://www.ncbi.nlm.nih.gov/pubmed/33594080
http://dx.doi.org/10.1038/s41467-021-21283-4
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author Kemper, Kathryn E.
Yengo, Loic
Zheng, Zhili
Abdellaoui, Abdel
Keller, Matthew C.
Goddard, Michael E.
Wray, Naomi R.
Yang, Jian
Visscher, Peter M.
author_facet Kemper, Kathryn E.
Yengo, Loic
Zheng, Zhili
Abdellaoui, Abdel
Keller, Matthew C.
Goddard, Michael E.
Wray, Naomi R.
Yang, Jian
Visscher, Peter M.
author_sort Kemper, Kathryn E.
collection PubMed
description Attributing the similarity between individuals to genetic and non-genetic factors is central to genetic analyses. In this paper we use the genomic relationship ([Formula: see text] ) among 417,060 individuals to investigate the phenotypic covariance between pairs of individuals for 32 traits across the spectrum of relatedness, from unrelated pairs through to identical twins. We find linear relationships between phenotypic covariance and [Formula: see text] that agree with the SNP-based heritability ([Formula: see text] ) in unrelated pairs ([Formula: see text] ), and with pedigree-estimated heritability in close relatives ([Formula: see text] ). The covariance increases faster than [Formula: see text] in distant relatives ([Formula: see text] ), and we attribute this to imperfect linkage disequilibrium between causal variants and the common variants used to construct [Formula: see text] . We also examine the effect of assortative mating on heritability estimates from different experimental designs. We find that full-sib identity-by-descent regression estimates for height (0.66 s.e. 0.07) are consistent with estimates from close relatives (0.82 s.e. 0.04) after accounting for the effect of assortative mating.
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spelling pubmed-78868992021-03-03 Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals Kemper, Kathryn E. Yengo, Loic Zheng, Zhili Abdellaoui, Abdel Keller, Matthew C. Goddard, Michael E. Wray, Naomi R. Yang, Jian Visscher, Peter M. Nat Commun Article Attributing the similarity between individuals to genetic and non-genetic factors is central to genetic analyses. In this paper we use the genomic relationship ([Formula: see text] ) among 417,060 individuals to investigate the phenotypic covariance between pairs of individuals for 32 traits across the spectrum of relatedness, from unrelated pairs through to identical twins. We find linear relationships between phenotypic covariance and [Formula: see text] that agree with the SNP-based heritability ([Formula: see text] ) in unrelated pairs ([Formula: see text] ), and with pedigree-estimated heritability in close relatives ([Formula: see text] ). The covariance increases faster than [Formula: see text] in distant relatives ([Formula: see text] ), and we attribute this to imperfect linkage disequilibrium between causal variants and the common variants used to construct [Formula: see text] . We also examine the effect of assortative mating on heritability estimates from different experimental designs. We find that full-sib identity-by-descent regression estimates for height (0.66 s.e. 0.07) are consistent with estimates from close relatives (0.82 s.e. 0.04) after accounting for the effect of assortative mating. Nature Publishing Group UK 2021-02-16 /pmc/articles/PMC7886899/ /pubmed/33594080 http://dx.doi.org/10.1038/s41467-021-21283-4 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kemper, Kathryn E.
Yengo, Loic
Zheng, Zhili
Abdellaoui, Abdel
Keller, Matthew C.
Goddard, Michael E.
Wray, Naomi R.
Yang, Jian
Visscher, Peter M.
Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals
title Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals
title_full Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals
title_fullStr Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals
title_full_unstemmed Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals
title_short Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals
title_sort phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886899/
https://www.ncbi.nlm.nih.gov/pubmed/33594080
http://dx.doi.org/10.1038/s41467-021-21283-4
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