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SMSSVD: SubMatrix Selection Singular Value Decomposition
MOTIVATION: High throughput biomedical measurements normally capture multiple overlaid biologically relevant signals and often also signals representing different types of technical artefacts like e.g. batch effects. Signal identification and decomposition are accordingly main objectives in statisti...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361234/ https://www.ncbi.nlm.nih.gov/pubmed/30010791 http://dx.doi.org/10.1093/bioinformatics/bty566 |
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author | Henningsson, Rasmus Fontes, Magnus |
author_facet | Henningsson, Rasmus Fontes, Magnus |
author_sort | Henningsson, Rasmus |
collection | PubMed |
description | MOTIVATION: High throughput biomedical measurements normally capture multiple overlaid biologically relevant signals and often also signals representing different types of technical artefacts like e.g. batch effects. Signal identification and decomposition are accordingly main objectives in statistical biomedical modeling and data analysis. Existing methods, aimed at signal reconstruction and deconvolution, in general, are either supervised, contain parameters that need to be estimated or present other types of ad hoc features. We here introduce SubMatrix Selection Singular Value Decomposition (SMSSVD), a parameter-free unsupervised signal decomposition and dimension reduction method, designed to reduce noise, adaptively for each low-rank-signal in a given data matrix, and represent the signals in the data in a way that enable unbiased exploratory analysis and reconstruction of multiple overlaid signals, including identifying groups of variables that drive different signals. RESULTS: The SMSSVD method produces a denoised signal decomposition from a given data matrix. It also guarantees orthogonality between signal components in a straightforward manner and it is designed to make automation possible. We illustrate SMSSVD by applying it to several real and synthetic datasets and compare its performance to golden standard methods like PCA (Principal Component Analysis) and SPC (Sparse Principal Components, using Lasso constraints). The SMSSVD is computationally efficient and despite being a parameter-free method, in general, outperforms existing statistical learning methods. AVAILABILITY AND IMPLEMENTATION: A Julia implementation of SMSSVD is openly available on GitHub (https://github.com/rasmushenningsson/SubMatrixSelectionSVD.jl). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-6361234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63612342019-02-08 SMSSVD: SubMatrix Selection Singular Value Decomposition Henningsson, Rasmus Fontes, Magnus Bioinformatics Original Papers MOTIVATION: High throughput biomedical measurements normally capture multiple overlaid biologically relevant signals and often also signals representing different types of technical artefacts like e.g. batch effects. Signal identification and decomposition are accordingly main objectives in statistical biomedical modeling and data analysis. Existing methods, aimed at signal reconstruction and deconvolution, in general, are either supervised, contain parameters that need to be estimated or present other types of ad hoc features. We here introduce SubMatrix Selection Singular Value Decomposition (SMSSVD), a parameter-free unsupervised signal decomposition and dimension reduction method, designed to reduce noise, adaptively for each low-rank-signal in a given data matrix, and represent the signals in the data in a way that enable unbiased exploratory analysis and reconstruction of multiple overlaid signals, including identifying groups of variables that drive different signals. RESULTS: The SMSSVD method produces a denoised signal decomposition from a given data matrix. It also guarantees orthogonality between signal components in a straightforward manner and it is designed to make automation possible. We illustrate SMSSVD by applying it to several real and synthetic datasets and compare its performance to golden standard methods like PCA (Principal Component Analysis) and SPC (Sparse Principal Components, using Lasso constraints). The SMSSVD is computationally efficient and despite being a parameter-free method, in general, outperforms existing statistical learning methods. AVAILABILITY AND IMPLEMENTATION: A Julia implementation of SMSSVD is openly available on GitHub (https://github.com/rasmushenningsson/SubMatrixSelectionSVD.jl). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2019-02-01 2018-07-13 /pmc/articles/PMC6361234/ /pubmed/30010791 http://dx.doi.org/10.1093/bioinformatics/bty566 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Henningsson, Rasmus Fontes, Magnus SMSSVD: SubMatrix Selection Singular Value Decomposition |
title | SMSSVD: SubMatrix Selection Singular Value Decomposition |
title_full | SMSSVD: SubMatrix Selection Singular Value Decomposition |
title_fullStr | SMSSVD: SubMatrix Selection Singular Value Decomposition |
title_full_unstemmed | SMSSVD: SubMatrix Selection Singular Value Decomposition |
title_short | SMSSVD: SubMatrix Selection Singular Value Decomposition |
title_sort | smssvd: submatrix selection singular value decomposition |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361234/ https://www.ncbi.nlm.nih.gov/pubmed/30010791 http://dx.doi.org/10.1093/bioinformatics/bty566 |
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