A hybrid approach of gene sets and single genes for the prediction of survival risks with gene expression data
Accumulated biological knowledge is often encoded as gene sets, collections of genes associated with similar biological functions or pathways. The use of gene sets in the analyses of high-throughput gene expression data has been intensively studied and applied in clinical research. However, the main...
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description | Accumulated biological knowledge is often encoded as gene sets, collections of genes associated with similar biological functions or pathways. The use of gene sets in the analyses of high-throughput gene expression data has been intensively studied and applied in clinical research. However, the main interest remains in finding modules of biological knowledge, or corresponding gene sets, significantly associated with disease conditions. Risk prediction from censored survival times using gene sets hasn't been well studied. In this work, we propose a hybrid method that uses both single gene and gene set information together to predict patient survival risks from gene expression profiles. In the proposed method, gene sets provide context-level information that is poorly reflected by single genes. Complementarily, single genes help to supplement incomplete information of gene sets due to our imperfect biomedical knowledge. Through the tests over multiple data sets of cancer and trauma injury, the proposed method showed robust and improved performance compared with the conventional approaches with only single genes or gene sets solely. Additionally, we examined the prediction result in the trauma injury data, and showed that the modules of biological knowledge used in the prediction by the proposed method were highly interpretable in biology. A wide range of survival prediction problems in clinical genomics is expected to benefit from the use of biological knowledge. |
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The use of gene sets in the analyses of high-throughput gene expression data has been intensively studied and applied in clinical research. However, the main interest remains in finding modules of biological knowledge, or corresponding gene sets, significantly associated with disease conditions. Risk prediction from censored survival times using gene sets hasn't been well studied. In this work, we propose a hybrid method that uses both single gene and gene set information together to predict patient survival risks from gene expression profiles. In the proposed method, gene sets provide context-level information that is poorly reflected by single genes. Complementarily, single genes help to supplement incomplete information of gene sets due to our imperfect biomedical knowledge. Through the tests over multiple data sets of cancer and trauma injury, the proposed method showed robust and improved performance compared with the conventional approaches with only single genes or gene sets solely. Additionally, we examined the prediction result in the trauma injury data, and showed that the modules of biological knowledge used in the prediction by the proposed method were highly interpretable in biology. A wide range of survival prediction problems in clinical genomics is expected to benefit from the use of biological knowledge.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0122103</identifier><identifier>PMID: 25933378</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Algorithms ; Bioaccumulation ; Bioinformatics ; Biology ; Breast cancer ; Cancer ; Classification ; Clinical outcomes ; Collections ; Computational Biology - methods ; Data collection ; Databases, Genetic ; Disease ; Gene expression ; Gene Expression Regulation ; Genes ; Genomes ; Genomics ; Health risks ; Humans ; Knowledge ; Lymphoma ; Medical prognosis ; Modules ; Multiple myeloma ; Principal components analysis ; Risk Factors ; Survival ; Survival Analysis ; Trauma ; Wounds and Injuries - genetics</subject><ispartof>PloS one, 2015-05, Vol.10 (5), p.e0122103-e0122103</ispartof><rights>2015 Seok et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Seok et al 2015 Seok et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-d0685d0f50af51176f2c7ff8de583bb35123a9940133b702520dcc7210cf99743</citedby><cites>FETCH-LOGICAL-c526t-d0685d0f50af51176f2c7ff8de583bb35123a9940133b702520dcc7210cf99743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416884/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416884/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25933378$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Lo, Anthony W.I.</contributor><creatorcontrib>Seok, Junhee</creatorcontrib><creatorcontrib>Davis, Ronald W</creatorcontrib><creatorcontrib>Xiao, Wenzhong</creatorcontrib><title>A hybrid approach of gene sets and single genes for the prediction of survival risks with gene expression data</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Accumulated biological knowledge is often encoded as gene sets, collections of genes associated with similar biological functions or pathways. The use of gene sets in the analyses of high-throughput gene expression data has been intensively studied and applied in clinical research. However, the main interest remains in finding modules of biological knowledge, or corresponding gene sets, significantly associated with disease conditions. Risk prediction from censored survival times using gene sets hasn't been well studied. In this work, we propose a hybrid method that uses both single gene and gene set information together to predict patient survival risks from gene expression profiles. In the proposed method, gene sets provide context-level information that is poorly reflected by single genes. Complementarily, single genes help to supplement incomplete information of gene sets due to our imperfect biomedical knowledge. Through the tests over multiple data sets of cancer and trauma injury, the proposed method showed robust and improved performance compared with the conventional approaches with only single genes or gene sets solely. Additionally, we examined the prediction result in the trauma injury data, and showed that the modules of biological knowledge used in the prediction by the proposed method were highly interpretable in biology. A wide range of survival prediction problems in clinical genomics is expected to benefit from the use of biological knowledge.</description><subject>Algorithms</subject><subject>Bioaccumulation</subject><subject>Bioinformatics</subject><subject>Biology</subject><subject>Breast cancer</subject><subject>Cancer</subject><subject>Classification</subject><subject>Clinical outcomes</subject><subject>Collections</subject><subject>Computational Biology - methods</subject><subject>Data collection</subject><subject>Databases, Genetic</subject><subject>Disease</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Genes</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Health risks</subject><subject>Humans</subject><subject>Knowledge</subject><subject>Lymphoma</subject><subject>Medical prognosis</subject><subject>Modules</subject><subject>Multiple myeloma</subject><subject>Principal components analysis</subject><subject>Risk Factors</subject><subject>Survival</subject><subject>Survival Analysis</subject><subject>Trauma</subject><subject>Wounds and Injuries - 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methods</topic><topic>Data collection</topic><topic>Databases, Genetic</topic><topic>Disease</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Genes</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Health risks</topic><topic>Humans</topic><topic>Knowledge</topic><topic>Lymphoma</topic><topic>Medical prognosis</topic><topic>Modules</topic><topic>Multiple myeloma</topic><topic>Principal components analysis</topic><topic>Risk Factors</topic><topic>Survival</topic><topic>Survival Analysis</topic><topic>Trauma</topic><topic>Wounds and Injuries - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seok, Junhee</creatorcontrib><creatorcontrib>Davis, Ronald W</creatorcontrib><creatorcontrib>Xiao, Wenzhong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seok, Junhee</au><au>Davis, Ronald W</au><au>Xiao, Wenzhong</au><au>Lo, Anthony W.I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A hybrid approach of gene sets and single genes for the prediction of survival risks with gene expression data</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-05-01</date><risdate>2015</risdate><volume>10</volume><issue>5</issue><spage>e0122103</spage><epage>e0122103</epage><pages>e0122103-e0122103</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Accumulated biological knowledge is often encoded as gene sets, collections of genes associated with similar biological functions or pathways. The use of gene sets in the analyses of high-throughput gene expression data has been intensively studied and applied in clinical research. However, the main interest remains in finding modules of biological knowledge, or corresponding gene sets, significantly associated with disease conditions. Risk prediction from censored survival times using gene sets hasn't been well studied. In this work, we propose a hybrid method that uses both single gene and gene set information together to predict patient survival risks from gene expression profiles. In the proposed method, gene sets provide context-level information that is poorly reflected by single genes. Complementarily, single genes help to supplement incomplete information of gene sets due to our imperfect biomedical knowledge. Through the tests over multiple data sets of cancer and trauma injury, the proposed method showed robust and improved performance compared with the conventional approaches with only single genes or gene sets solely. Additionally, we examined the prediction result in the trauma injury data, and showed that the modules of biological knowledge used in the prediction by the proposed method were highly interpretable in biology. A wide range of survival prediction problems in clinical genomics is expected to benefit from the use of biological knowledge.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25933378</pmid><doi>10.1371/journal.pone.0122103</doi><oa>free_for_read</oa></addata></record> |
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subjects | Algorithms Bioaccumulation Bioinformatics Biology Breast cancer Cancer Classification Clinical outcomes Collections Computational Biology - methods Data collection Databases, Genetic Disease Gene expression Gene Expression Regulation Genes Genomes Genomics Health risks Humans Knowledge Lymphoma Medical prognosis Modules Multiple myeloma Principal components analysis Risk Factors Survival Survival Analysis Trauma Wounds and Injuries - genetics |
title | A hybrid approach of gene sets and single genes for the prediction of survival risks with gene expression data |
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