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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Main Authors: Wei Xu, Huisong Wang, Wenqing Cheng, Dong Fu, Tian Xia, Warren A Kibbe, Simon M Lin
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3519466?pdf=render
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spelling doaj-c3c974a9349c4eec962f4bc8be06aaf62020-11-24T22:08:10ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01712e4968610.1371/journal.pone.0049686A framework for annotating human genome in disease context.Wei XuHuisong WangWenqing ChengDong FuTian XiaWarren A KibbeSimon M LinIdentification 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.http://europepmc.org/articles/PMC3519466?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Wei Xu
Huisong Wang
Wenqing Cheng
Dong Fu
Tian Xia
Warren A Kibbe
Simon M Lin
spellingShingle Wei Xu
Huisong Wang
Wenqing Cheng
Dong Fu
Tian Xia
Warren A Kibbe
Simon M Lin
A framework for annotating human genome in disease context.
PLoS ONE
author_facet Wei Xu
Huisong Wang
Wenqing Cheng
Dong Fu
Tian Xia
Warren A Kibbe
Simon M Lin
author_sort Wei Xu
title A framework for annotating human genome in disease context.
title_short A framework for annotating human genome in disease context.
title_full A framework for annotating human genome in disease context.
title_fullStr A framework for annotating human genome in disease context.
title_full_unstemmed A framework for annotating human genome in disease context.
title_sort framework for annotating human genome in disease context.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
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.
url http://europepmc.org/articles/PMC3519466?pdf=render
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