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Bayesian network-driven clustering analysis with feature selection for high-dimensional multi-modal molecular data
Multi-modal molecular profiling data in bulk tumors or single cells are accumulating at a fast pace. There is a great need for developing statistical and computational methods to reveal molecular structures in complex data types toward biological discoveries. Here, we introduce Nebula, a novel Bayes...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933297/ https://www.ncbi.nlm.nih.gov/pubmed/33664338 http://dx.doi.org/10.1038/s41598-021-84514-0 |
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author | Zhao, Yize Chang, Changgee Hannum, Margaret Lee, Jasme Shen, Ronglai |
author_facet | Zhao, Yize Chang, Changgee Hannum, Margaret Lee, Jasme Shen, Ronglai |
author_sort | Zhao, Yize |
collection | PubMed |
description | Multi-modal molecular profiling data in bulk tumors or single cells are accumulating at a fast pace. There is a great need for developing statistical and computational methods to reveal molecular structures in complex data types toward biological discoveries. Here, we introduce Nebula, a novel Bayesian integrative clustering analysis for high dimensional multi-modal molecular data to identify directly interpretable clusters and associated biomarkers in a unified and biologically plausible framework. To facilitate computational efficiency, a variational Bayes approach is developed to approximate the joint posterior distribution to achieve model inference in high-dimensional settings. We describe a pan-cancer data analysis of genomic, epigenomic, and transcriptomic alterations in close to 9000 tumor samples across canonical oncogenic signaling pathways, immune and stemness phenotype, with comparisons to state-of-the-art clustering methods. We demonstrate that Nebula has the unique advantage of revealing patterns on the basis of shared pathway alterations, offering biological and clinical insights beyond tumor type and histology in the pan-cancer analysis setting. We also illustrate the utility of Nebula in single cell data for immune cell decomposition in peripheral blood samples. |
format | Online Article Text |
id | pubmed-7933297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79332972021-03-08 Bayesian network-driven clustering analysis with feature selection for high-dimensional multi-modal molecular data Zhao, Yize Chang, Changgee Hannum, Margaret Lee, Jasme Shen, Ronglai Sci Rep Article Multi-modal molecular profiling data in bulk tumors or single cells are accumulating at a fast pace. There is a great need for developing statistical and computational methods to reveal molecular structures in complex data types toward biological discoveries. Here, we introduce Nebula, a novel Bayesian integrative clustering analysis for high dimensional multi-modal molecular data to identify directly interpretable clusters and associated biomarkers in a unified and biologically plausible framework. To facilitate computational efficiency, a variational Bayes approach is developed to approximate the joint posterior distribution to achieve model inference in high-dimensional settings. We describe a pan-cancer data analysis of genomic, epigenomic, and transcriptomic alterations in close to 9000 tumor samples across canonical oncogenic signaling pathways, immune and stemness phenotype, with comparisons to state-of-the-art clustering methods. We demonstrate that Nebula has the unique advantage of revealing patterns on the basis of shared pathway alterations, offering biological and clinical insights beyond tumor type and histology in the pan-cancer analysis setting. We also illustrate the utility of Nebula in single cell data for immune cell decomposition in peripheral blood samples. Nature Publishing Group UK 2021-03-04 /pmc/articles/PMC7933297/ /pubmed/33664338 http://dx.doi.org/10.1038/s41598-021-84514-0 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhao, Yize Chang, Changgee Hannum, Margaret Lee, Jasme Shen, Ronglai Bayesian network-driven clustering analysis with feature selection for high-dimensional multi-modal molecular data |
title | Bayesian network-driven clustering analysis with feature selection for high-dimensional multi-modal molecular data |
title_full | Bayesian network-driven clustering analysis with feature selection for high-dimensional multi-modal molecular data |
title_fullStr | Bayesian network-driven clustering analysis with feature selection for high-dimensional multi-modal molecular data |
title_full_unstemmed | Bayesian network-driven clustering analysis with feature selection for high-dimensional multi-modal molecular data |
title_short | Bayesian network-driven clustering analysis with feature selection for high-dimensional multi-modal molecular data |
title_sort | bayesian network-driven clustering analysis with feature selection for high-dimensional multi-modal molecular data |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933297/ https://www.ncbi.nlm.nih.gov/pubmed/33664338 http://dx.doi.org/10.1038/s41598-021-84514-0 |
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