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Genotype Value Decomposition: Simple Methods for the Computation of Kernel Statistics

Recent advances in sequencing technologies enable genome‐wide analyses for thousands of individuals. The sequential kernel association test (SKAT) is a widely used method to test for associations between a phenotype and a set of rare variants. As the sample size of human genetics studies increases,...

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Autor principal: Misawa, Kazuharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744480/
https://www.ncbi.nlm.nih.gov/pubmed/36620199
http://dx.doi.org/10.1002/ggn2.202100066
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author Misawa, Kazuharu
author_facet Misawa, Kazuharu
author_sort Misawa, Kazuharu
collection PubMed
description Recent advances in sequencing technologies enable genome‐wide analyses for thousands of individuals. The sequential kernel association test (SKAT) is a widely used method to test for associations between a phenotype and a set of rare variants. As the sample size of human genetics studies increases, the computational time required to calculate a kernel is becoming more and more problematic. In this study, a new method to obtain kernel statistics without calculating a kernel matrix is proposed. A simple method for the computation of two kernel statistics, namely, a kernel statistic based on a genetic relationship matrix (GRM) and one based on an identity by state (IBS) matrix, are proposed. By using this method, calculation of the kernel statistics can be conducted using vector calculation without matrix calculation. The proposed method enables one to conduct SKAT for large samples of human genetics.
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spelling pubmed-97444802023-01-06 Genotype Value Decomposition: Simple Methods for the Computation of Kernel Statistics Misawa, Kazuharu Adv Genet (Hoboken) Research Articles Recent advances in sequencing technologies enable genome‐wide analyses for thousands of individuals. The sequential kernel association test (SKAT) is a widely used method to test for associations between a phenotype and a set of rare variants. As the sample size of human genetics studies increases, the computational time required to calculate a kernel is becoming more and more problematic. In this study, a new method to obtain kernel statistics without calculating a kernel matrix is proposed. A simple method for the computation of two kernel statistics, namely, a kernel statistic based on a genetic relationship matrix (GRM) and one based on an identity by state (IBS) matrix, are proposed. By using this method, calculation of the kernel statistics can be conducted using vector calculation without matrix calculation. The proposed method enables one to conduct SKAT for large samples of human genetics. John Wiley and Sons Inc. 2022-04-05 /pmc/articles/PMC9744480/ /pubmed/36620199 http://dx.doi.org/10.1002/ggn2.202100066 Text en © 2022 The Authors. Advanced Genetics published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Misawa, Kazuharu
Genotype Value Decomposition: Simple Methods for the Computation of Kernel Statistics
title Genotype Value Decomposition: Simple Methods for the Computation of Kernel Statistics
title_full Genotype Value Decomposition: Simple Methods for the Computation of Kernel Statistics
title_fullStr Genotype Value Decomposition: Simple Methods for the Computation of Kernel Statistics
title_full_unstemmed Genotype Value Decomposition: Simple Methods for the Computation of Kernel Statistics
title_short Genotype Value Decomposition: Simple Methods for the Computation of Kernel Statistics
title_sort genotype value decomposition: simple methods for the computation of kernel statistics
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744480/
https://www.ncbi.nlm.nih.gov/pubmed/36620199
http://dx.doi.org/10.1002/ggn2.202100066
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