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Subtype identification from heterogeneous TCGA datasets on a genomic scale by multi-view clustering with enhanced consensus
BACKGROUND: The Cancer Genome Atlas (TCGA) has collected transcriptome, genome and epigenome information for over 20 cancers from thousands of patients. The availability of these diverse data types makes it necessary to combine these data to capture the heterogeneity of biological processes and phen...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763310/ https://www.ncbi.nlm.nih.gov/pubmed/29322925 http://dx.doi.org/10.1186/s12920-017-0306-x |
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author | Cai, Menglan Li, Limin |
author_facet | Cai, Menglan Li, Limin |
author_sort | Cai, Menglan |
collection | PubMed |
description | BACKGROUND: The Cancer Genome Atlas (TCGA) has collected transcriptome, genome and epigenome information for over 20 cancers from thousands of patients. The availability of these diverse data types makes it necessary to combine these data to capture the heterogeneity of biological processes and phenotypes and further identify homogeneous subtypes for cancers such as breast cancer. Many multi-view clustering approaches are proposed to discover clusters across different data types. The problem is challenging when different data types show poor agreement of clustering structure. RESULTS: In this work, we first propose a multi-view clustering approach with consensus (CMC), which tries to find consensus kernels among views by using Hilbert Schmidt Independence Criterion. To tackle the problem when poor agreement among views exists, we further propose a multi-view clustering approach with enhanced consensus (ECMC) to solve this problem by decomposing the kernel information in each view into a consensus part and a disagreement part. The consensus parts for different views are supposed to be similar, and the disagreement parts should be independent with the consensus parts. Both the CMC and ECMC models can be solved by alternative updating with semi-definite programming. Our experiments on both simulation datasets and real-world benchmark datasets show that ECMC model could achieve higher clustering accuracies than other state-of-art multi-view clustering approaches. We also apply the ECMC model to integrate mRNA expression, DNA methylation and microRNA (miRNA) expression data for five cancer data sets, and the survival analysis show that our ECMC model outperforms other methods when identifying cancer subtypes. By Fisher’s combination test method, we found that three computed subtypes roughly correspond to three known breast cancer subtypes including luminal B, HER2 and basal-like subtypes. CONCLUSION: Integrating heterogeneous TCGA datasets by our proposed multi-view clustering approach ECMC could effectively identify cancer subtypes. |
format | Online Article Text |
id | pubmed-5763310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57633102018-01-17 Subtype identification from heterogeneous TCGA datasets on a genomic scale by multi-view clustering with enhanced consensus Cai, Menglan Li, Limin BMC Med Genomics Research BACKGROUND: The Cancer Genome Atlas (TCGA) has collected transcriptome, genome and epigenome information for over 20 cancers from thousands of patients. The availability of these diverse data types makes it necessary to combine these data to capture the heterogeneity of biological processes and phenotypes and further identify homogeneous subtypes for cancers such as breast cancer. Many multi-view clustering approaches are proposed to discover clusters across different data types. The problem is challenging when different data types show poor agreement of clustering structure. RESULTS: In this work, we first propose a multi-view clustering approach with consensus (CMC), which tries to find consensus kernels among views by using Hilbert Schmidt Independence Criterion. To tackle the problem when poor agreement among views exists, we further propose a multi-view clustering approach with enhanced consensus (ECMC) to solve this problem by decomposing the kernel information in each view into a consensus part and a disagreement part. The consensus parts for different views are supposed to be similar, and the disagreement parts should be independent with the consensus parts. Both the CMC and ECMC models can be solved by alternative updating with semi-definite programming. Our experiments on both simulation datasets and real-world benchmark datasets show that ECMC model could achieve higher clustering accuracies than other state-of-art multi-view clustering approaches. We also apply the ECMC model to integrate mRNA expression, DNA methylation and microRNA (miRNA) expression data for five cancer data sets, and the survival analysis show that our ECMC model outperforms other methods when identifying cancer subtypes. By Fisher’s combination test method, we found that three computed subtypes roughly correspond to three known breast cancer subtypes including luminal B, HER2 and basal-like subtypes. CONCLUSION: Integrating heterogeneous TCGA datasets by our proposed multi-view clustering approach ECMC could effectively identify cancer subtypes. BioMed Central 2017-12-21 /pmc/articles/PMC5763310/ /pubmed/29322925 http://dx.doi.org/10.1186/s12920-017-0306-x Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Cai, Menglan Li, Limin Subtype identification from heterogeneous TCGA datasets on a genomic scale by multi-view clustering with enhanced consensus |
title | Subtype identification from heterogeneous TCGA datasets on a genomic scale by multi-view clustering with enhanced consensus |
title_full | Subtype identification from heterogeneous TCGA datasets on a genomic scale by multi-view clustering with enhanced consensus |
title_fullStr | Subtype identification from heterogeneous TCGA datasets on a genomic scale by multi-view clustering with enhanced consensus |
title_full_unstemmed | Subtype identification from heterogeneous TCGA datasets on a genomic scale by multi-view clustering with enhanced consensus |
title_short | Subtype identification from heterogeneous TCGA datasets on a genomic scale by multi-view clustering with enhanced consensus |
title_sort | subtype identification from heterogeneous tcga datasets on a genomic scale by multi-view clustering with enhanced consensus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763310/ https://www.ncbi.nlm.nih.gov/pubmed/29322925 http://dx.doi.org/10.1186/s12920-017-0306-x |
work_keys_str_mv | AT caimenglan subtypeidentificationfromheterogeneoustcgadatasetsonagenomicscalebymultiviewclusteringwithenhancedconsensus AT lilimin subtypeidentificationfromheterogeneoustcgadatasetsonagenomicscalebymultiviewclusteringwithenhancedconsensus |