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Kinship Solutions for Partially Observed Multiphenotype Data
Current work for multivariate analysis of phenotypes in genome-wide association studies often requires that genetic similarity matrices be inverted or decomposed. This can be a computational bottleneck when many phenotypes are presented, each with a different missingness pattern. A usual method in t...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc., publishers
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482112/ https://www.ncbi.nlm.nih.gov/pubmed/32159382 http://dx.doi.org/10.1089/cmb.2019.0440 |
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author | Elliott, Lloyd T. |
author_facet | Elliott, Lloyd T. |
author_sort | Elliott, Lloyd T. |
collection | PubMed |
description | Current work for multivariate analysis of phenotypes in genome-wide association studies often requires that genetic similarity matrices be inverted or decomposed. This can be a computational bottleneck when many phenotypes are presented, each with a different missingness pattern. A usual method in this case is to perform decompositions on subsets of the kinship matrix for each phenotype, with each subset corresponding to the set of observed samples for that phenotype. We provide a new method for decomposing these kinship matrices that can reduce the computational complexity by an order of magnitude by propagating low-rank modifications along a tree spanning the phenotypes. We demonstrate that our method provides speed improvements of around 40% under reasonable conditions. |
format | Online Article Text |
id | pubmed-7482112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Mary Ann Liebert, Inc., publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-74821122020-09-11 Kinship Solutions for Partially Observed Multiphenotype Data Elliott, Lloyd T. J Comput Biol Research Articles Current work for multivariate analysis of phenotypes in genome-wide association studies often requires that genetic similarity matrices be inverted or decomposed. This can be a computational bottleneck when many phenotypes are presented, each with a different missingness pattern. A usual method in this case is to perform decompositions on subsets of the kinship matrix for each phenotype, with each subset corresponding to the set of observed samples for that phenotype. We provide a new method for decomposing these kinship matrices that can reduce the computational complexity by an order of magnitude by propagating low-rank modifications along a tree spanning the phenotypes. We demonstrate that our method provides speed improvements of around 40% under reasonable conditions. Mary Ann Liebert, Inc., publishers 2020-09-01 2020-09-04 /pmc/articles/PMC7482112/ /pubmed/32159382 http://dx.doi.org/10.1089/cmb.2019.0440 Text en © Lloyd T. Elliott, 2020. Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Research Articles Elliott, Lloyd T. Kinship Solutions for Partially Observed Multiphenotype Data |
title | Kinship Solutions for Partially Observed Multiphenotype Data |
title_full | Kinship Solutions for Partially Observed Multiphenotype Data |
title_fullStr | Kinship Solutions for Partially Observed Multiphenotype Data |
title_full_unstemmed | Kinship Solutions for Partially Observed Multiphenotype Data |
title_short | Kinship Solutions for Partially Observed Multiphenotype Data |
title_sort | kinship solutions for partially observed multiphenotype data |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482112/ https://www.ncbi.nlm.nih.gov/pubmed/32159382 http://dx.doi.org/10.1089/cmb.2019.0440 |
work_keys_str_mv | AT elliottlloydt kinshipsolutionsforpartiallyobservedmultiphenotypedata |