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Maximal Perfect Haplotype Blocks with Wildcards
Recent work provides the first method to measure the relative fitness of genomic variants within a population that scales to large numbers of genomes. A key component of the computation involves finding maximal perfect haplotype blocks from a set of genomic samples for which SNPs (single-nucleotide...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7243190/ https://www.ncbi.nlm.nih.gov/pubmed/32446220 http://dx.doi.org/10.1016/j.isci.2020.101149 |
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author | Williams, Lucia Mumey, Brendan |
author_facet | Williams, Lucia Mumey, Brendan |
author_sort | Williams, Lucia |
collection | PubMed |
description | Recent work provides the first method to measure the relative fitness of genomic variants within a population that scales to large numbers of genomes. A key component of the computation involves finding maximal perfect haplotype blocks from a set of genomic samples for which SNPs (single-nucleotide polymorphisms) have been called. Often, owing to low read coverage and imperfect assemblies, some of the SNP calls can be missing from some of the samples. In this work, we consider the problem of finding maximal perfect haplotype blocks where some missing values may be present. Missing values are treated as wildcards, and the definition of maximal perfect haplotype blocks is extended in a natural way. We provide an output-linear time algorithm to identify all such blocks and demonstrate the algorithm on a large population SNP dataset. Our software is publicly available. |
format | Online Article Text |
id | pubmed-7243190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-72431902020-05-26 Maximal Perfect Haplotype Blocks with Wildcards Williams, Lucia Mumey, Brendan iScience Article Recent work provides the first method to measure the relative fitness of genomic variants within a population that scales to large numbers of genomes. A key component of the computation involves finding maximal perfect haplotype blocks from a set of genomic samples for which SNPs (single-nucleotide polymorphisms) have been called. Often, owing to low read coverage and imperfect assemblies, some of the SNP calls can be missing from some of the samples. In this work, we consider the problem of finding maximal perfect haplotype blocks where some missing values may be present. Missing values are treated as wildcards, and the definition of maximal perfect haplotype blocks is extended in a natural way. We provide an output-linear time algorithm to identify all such blocks and demonstrate the algorithm on a large population SNP dataset. Our software is publicly available. Elsevier 2020-05-11 /pmc/articles/PMC7243190/ /pubmed/32446220 http://dx.doi.org/10.1016/j.isci.2020.101149 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Williams, Lucia Mumey, Brendan Maximal Perfect Haplotype Blocks with Wildcards |
title | Maximal Perfect Haplotype Blocks with Wildcards |
title_full | Maximal Perfect Haplotype Blocks with Wildcards |
title_fullStr | Maximal Perfect Haplotype Blocks with Wildcards |
title_full_unstemmed | Maximal Perfect Haplotype Blocks with Wildcards |
title_short | Maximal Perfect Haplotype Blocks with Wildcards |
title_sort | maximal perfect haplotype blocks with wildcards |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7243190/ https://www.ncbi.nlm.nih.gov/pubmed/32446220 http://dx.doi.org/10.1016/j.isci.2020.101149 |
work_keys_str_mv | AT williamslucia maximalperfecthaplotypeblockswithwildcards AT mumeybrendan maximalperfecthaplotypeblockswithwildcards |