A framework for annotating human genome in disease context
Identification of gene-disease association is crucial to understanding disease mechanism. A rapid increase in biomedical literatures, led by advances of genome-scale technologies, poses challenge for manually-curated-based annotation databases to characterize gene-disease associations effectively an...
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creator | Xu, Wei Wang, Huisong Cheng, Wenqing Fu, Dong Xia, Tian Kibbe, Warren A Lin, Simon M |
description | Identification of gene-disease association is crucial to understanding disease mechanism. A rapid increase in biomedical literatures, led by advances of genome-scale technologies, poses challenge for manually-curated-based annotation databases to characterize gene-disease associations effectively and timely. We propose an automatic method-The Disease Ontology Annotation Framework (DOAF) to provide a comprehensive annotation of the human genome using the computable Disease Ontology (DO), the NCBO Annotator service and NCBI Gene Reference Into Function (GeneRIF). DOAF can keep the resulting knowledgebase current by periodically executing automatic pipeline to re-annotate the human genome using the latest DO and GeneRIF releases at any frequency such as daily or monthly. Further, DOAF provides a computable and programmable environment which enables large-scale and integrative analysis by working with external analytic software or online service platforms. A user-friendly web interface (doa.nubic.northwestern.edu) is implemented to allow users to efficiently query, download, and view disease annotations and the underlying evidences. |
doi_str_mv | 10.1371/journal.pone.0049686 |
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A rapid increase in biomedical literatures, led by advances of genome-scale technologies, poses challenge for manually-curated-based annotation databases to characterize gene-disease associations effectively and timely. We propose an automatic method-The Disease Ontology Annotation Framework (DOAF) to provide a comprehensive annotation of the human genome using the computable Disease Ontology (DO), the NCBO Annotator service and NCBI Gene Reference Into Function (GeneRIF). DOAF can keep the resulting knowledgebase current by periodically executing automatic pipeline to re-annotate the human genome using the latest DO and GeneRIF releases at any frequency such as daily or monthly. Further, DOAF provides a computable and programmable environment which enables large-scale and integrative analysis by working with external analytic software or online service platforms. A user-friendly web interface (doa.nubic.northwestern.edu) is implemented to allow users to efficiently query, download, and view disease annotations and the underlying evidences.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0049686</identifier><identifier>PMID: 23251346</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Annotations ; Anopheles ; Bioinformatics ; Biology ; Cancer ; Computational Biology - methods ; Controlled vocabularies ; Databases, Genetic ; Disease ; Downloading ; Engineering ; Genes ; Genetic Predisposition to Disease ; Genome, Human ; Genomes ; Genomics ; Humans ; Informatics ; Knowledge base ; Medicine ; Natural language processing ; Ontology ; Semantics ; Social and Behavioral Sciences ; Software ; Vocabulary, Controlled</subject><ispartof>PloS one, 2012-12, Vol.7 (12), p.e49686-e49686</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Xu et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://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>2012 Xu et al 2012 Xu et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c758t-366f65496cd69963e9c739323603c39054552a4722b84a6fe920896aaeeeb69e3</citedby><cites>FETCH-LOGICAL-c758t-366f65496cd69963e9c739323603c39054552a4722b84a6fe920896aaeeeb69e3</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/PMC3519466/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519466/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79343,79344</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23251346$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Wei</creatorcontrib><creatorcontrib>Wang, Huisong</creatorcontrib><creatorcontrib>Cheng, Wenqing</creatorcontrib><creatorcontrib>Fu, Dong</creatorcontrib><creatorcontrib>Xia, Tian</creatorcontrib><creatorcontrib>Kibbe, Warren A</creatorcontrib><creatorcontrib>Lin, Simon M</creatorcontrib><title>A framework for annotating human genome in disease context</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Identification of gene-disease association is crucial to understanding disease mechanism. A rapid increase in biomedical literatures, led by advances of genome-scale technologies, poses challenge for manually-curated-based annotation databases to characterize gene-disease associations effectively and timely. We propose an automatic method-The Disease Ontology Annotation Framework (DOAF) to provide a comprehensive annotation of the human genome using the computable Disease Ontology (DO), the NCBO Annotator service and NCBI Gene Reference Into Function (GeneRIF). DOAF can keep the resulting knowledgebase current by periodically executing automatic pipeline to re-annotate the human genome using the latest DO and GeneRIF releases at any frequency such as daily or monthly. Further, DOAF provides a computable and programmable environment which enables large-scale and integrative analysis by working with external analytic software or online service platforms. 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A rapid increase in biomedical literatures, led by advances of genome-scale technologies, poses challenge for manually-curated-based annotation databases to characterize gene-disease associations effectively and timely. We propose an automatic method-The Disease Ontology Annotation Framework (DOAF) to provide a comprehensive annotation of the human genome using the computable Disease Ontology (DO), the NCBO Annotator service and NCBI Gene Reference Into Function (GeneRIF). DOAF can keep the resulting knowledgebase current by periodically executing automatic pipeline to re-annotate the human genome using the latest DO and GeneRIF releases at any frequency such as daily or monthly. Further, DOAF provides a computable and programmable environment which enables large-scale and integrative analysis by working with external analytic software or online service platforms. 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subjects | Annotations Anopheles Bioinformatics Biology Cancer Computational Biology - methods Controlled vocabularies Databases, Genetic Disease Downloading Engineering Genes Genetic Predisposition to Disease Genome, Human Genomes Genomics Humans Informatics Knowledge base Medicine Natural language processing Ontology Semantics Social and Behavioral Sciences Software Vocabulary, Controlled |
title | A framework for annotating human genome in disease context |
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