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Fast, low-memory detection and localization of large, polymorphic inversions from SNPs
BACKGROUND: Large (>1 Mb), polymorphic inversions have substantial impacts on population structure and maintenance of genotypes. These large inversions can be detected from single nucleotide polymorphism (SNP) data using unsupervised learning techniques like PCA. Construction and analysis of a fe...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784018/ https://www.ncbi.nlm.nih.gov/pubmed/35116204 http://dx.doi.org/10.7717/peerj.12831 |
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author | Nowling, Ronald J. Fallas-Moya, Fabian Sadovnik, Amir Emrich, Scott Aleck, Matthew Leskiewicz, Daniel Peters, John G. |
author_facet | Nowling, Ronald J. Fallas-Moya, Fabian Sadovnik, Amir Emrich, Scott Aleck, Matthew Leskiewicz, Daniel Peters, John G. |
author_sort | Nowling, Ronald J. |
collection | PubMed |
description | BACKGROUND: Large (>1 Mb), polymorphic inversions have substantial impacts on population structure and maintenance of genotypes. These large inversions can be detected from single nucleotide polymorphism (SNP) data using unsupervised learning techniques like PCA. Construction and analysis of a feature matrix from millions of SNPs requires large amount of memory and limits the sizes of data sets that can be analyzed. METHODS: We propose using feature hashing construct a feature matrix from a VCF file of SNPs for reducing memory usage. The matrix is constructed in a streaming fashion such that the entire VCF file is never loaded into memory at one time. RESULTS: When evaluated on Anopheles mosquito and Drosophila fly data sets, our approach reduced memory usage by 97% with minimal reductions in accuracy for inversion detection and localization tasks. CONCLUSION: With these changes, inversions in larger data sets can be analyzed easily and efficiently on common laptop and desktop computers. Our method is publicly available through our open-source inversion analysis software, Asaph. |
format | Online Article Text |
id | pubmed-8784018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87840182022-02-02 Fast, low-memory detection and localization of large, polymorphic inversions from SNPs Nowling, Ronald J. Fallas-Moya, Fabian Sadovnik, Amir Emrich, Scott Aleck, Matthew Leskiewicz, Daniel Peters, John G. PeerJ Bioinformatics BACKGROUND: Large (>1 Mb), polymorphic inversions have substantial impacts on population structure and maintenance of genotypes. These large inversions can be detected from single nucleotide polymorphism (SNP) data using unsupervised learning techniques like PCA. Construction and analysis of a feature matrix from millions of SNPs requires large amount of memory and limits the sizes of data sets that can be analyzed. METHODS: We propose using feature hashing construct a feature matrix from a VCF file of SNPs for reducing memory usage. The matrix is constructed in a streaming fashion such that the entire VCF file is never loaded into memory at one time. RESULTS: When evaluated on Anopheles mosquito and Drosophila fly data sets, our approach reduced memory usage by 97% with minimal reductions in accuracy for inversion detection and localization tasks. CONCLUSION: With these changes, inversions in larger data sets can be analyzed easily and efficiently on common laptop and desktop computers. Our method is publicly available through our open-source inversion analysis software, Asaph. PeerJ Inc. 2022-01-20 /pmc/articles/PMC8784018/ /pubmed/35116204 http://dx.doi.org/10.7717/peerj.12831 Text en © 2022 Nowling et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Bioinformatics Nowling, Ronald J. Fallas-Moya, Fabian Sadovnik, Amir Emrich, Scott Aleck, Matthew Leskiewicz, Daniel Peters, John G. Fast, low-memory detection and localization of large, polymorphic inversions from SNPs |
title | Fast, low-memory detection and localization of large, polymorphic inversions from SNPs |
title_full | Fast, low-memory detection and localization of large, polymorphic inversions from SNPs |
title_fullStr | Fast, low-memory detection and localization of large, polymorphic inversions from SNPs |
title_full_unstemmed | Fast, low-memory detection and localization of large, polymorphic inversions from SNPs |
title_short | Fast, low-memory detection and localization of large, polymorphic inversions from SNPs |
title_sort | fast, low-memory detection and localization of large, polymorphic inversions from snps |
topic | Bioinformatics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784018/ https://www.ncbi.nlm.nih.gov/pubmed/35116204 http://dx.doi.org/10.7717/peerj.12831 |
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