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MoSBi: Automated signature mining for molecular stratification and subtyping
The improving access to increasing amounts of biomedical data provides completely new chances for advanced patient stratification and disease subtyping strategies. This requires computational tools that produce uniformly robust results across highly heterogeneous molecular data. Unsupervised machine...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169782/ https://www.ncbi.nlm.nih.gov/pubmed/35412913 http://dx.doi.org/10.1073/pnas.2118210119 |
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author | Rose, Tim Daniel Bechtler, Thibault Ciora, Octavia-Andreea Anh Lilian Le, Kim Molnar, Florian Köhler, Nikolai Baumbach, Jan Röttger, Richard Pauling, Josch Konstantin |
author_facet | Rose, Tim Daniel Bechtler, Thibault Ciora, Octavia-Andreea Anh Lilian Le, Kim Molnar, Florian Köhler, Nikolai Baumbach, Jan Röttger, Richard Pauling, Josch Konstantin |
author_sort | Rose, Tim Daniel |
collection | PubMed |
description | The improving access to increasing amounts of biomedical data provides completely new chances for advanced patient stratification and disease subtyping strategies. This requires computational tools that produce uniformly robust results across highly heterogeneous molecular data. Unsupervised machine learning methodologies are able to discover de novo patterns in such data. Biclustering is especially suited by simultaneously identifying sample groups and corresponding feature sets across heterogeneous omics data. The performance of available biclustering algorithms heavily depends on individual parameterization and varies with their application. Here, we developed MoSBi (molecular signature identification using biclustering), an automated multialgorithm ensemble approach that integrates results utilizing an error model-supported similarity network. We systematically evaluated the performance of 11 available and established biclustering algorithms together with MoSBi. For this, we used transcriptomics, proteomics, and metabolomics data, as well as synthetic datasets covering various data properties. Profiting from multialgorithm integration, MoSBi identified robust group and disease-specific signatures across all scenarios, overcoming single algorithm specificities. Furthermore, we developed a scalable network-based visualization of bicluster communities that supports biological hypothesis generation. MoSBi is available as an R package and web service to make automated biclustering analysis accessible for application in molecular sample stratification. |
format | Online Article Text |
id | pubmed-9169782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-91697822022-06-07 MoSBi: Automated signature mining for molecular stratification and subtyping Rose, Tim Daniel Bechtler, Thibault Ciora, Octavia-Andreea Anh Lilian Le, Kim Molnar, Florian Köhler, Nikolai Baumbach, Jan Röttger, Richard Pauling, Josch Konstantin Proc Natl Acad Sci U S A Biological Sciences The improving access to increasing amounts of biomedical data provides completely new chances for advanced patient stratification and disease subtyping strategies. This requires computational tools that produce uniformly robust results across highly heterogeneous molecular data. Unsupervised machine learning methodologies are able to discover de novo patterns in such data. Biclustering is especially suited by simultaneously identifying sample groups and corresponding feature sets across heterogeneous omics data. The performance of available biclustering algorithms heavily depends on individual parameterization and varies with their application. Here, we developed MoSBi (molecular signature identification using biclustering), an automated multialgorithm ensemble approach that integrates results utilizing an error model-supported similarity network. We systematically evaluated the performance of 11 available and established biclustering algorithms together with MoSBi. For this, we used transcriptomics, proteomics, and metabolomics data, as well as synthetic datasets covering various data properties. Profiting from multialgorithm integration, MoSBi identified robust group and disease-specific signatures across all scenarios, overcoming single algorithm specificities. Furthermore, we developed a scalable network-based visualization of bicluster communities that supports biological hypothesis generation. MoSBi is available as an R package and web service to make automated biclustering analysis accessible for application in molecular sample stratification. National Academy of Sciences 2022-04-11 2022-04-19 /pmc/articles/PMC9169782/ /pubmed/35412913 http://dx.doi.org/10.1073/pnas.2118210119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Rose, Tim Daniel Bechtler, Thibault Ciora, Octavia-Andreea Anh Lilian Le, Kim Molnar, Florian Köhler, Nikolai Baumbach, Jan Röttger, Richard Pauling, Josch Konstantin MoSBi: Automated signature mining for molecular stratification and subtyping |
title | MoSBi: Automated signature mining for molecular stratification and subtyping |
title_full | MoSBi: Automated signature mining for molecular stratification and subtyping |
title_fullStr | MoSBi: Automated signature mining for molecular stratification and subtyping |
title_full_unstemmed | MoSBi: Automated signature mining for molecular stratification and subtyping |
title_short | MoSBi: Automated signature mining for molecular stratification and subtyping |
title_sort | mosbi: automated signature mining for molecular stratification and subtyping |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169782/ https://www.ncbi.nlm.nih.gov/pubmed/35412913 http://dx.doi.org/10.1073/pnas.2118210119 |
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