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HEDD: Human Enhancer Disease Database

Enhancers, as specialized genomic cis-regulatory elements, activate transcription of their target genes and play an important role in pathogenesis of many human complex diseases. Despite recent systematic identification of them in the human genome, currently there is an urgent need for comprehensive...

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Detalles Bibliográficos
Autores principales: Wang, Zhen, Zhang, Quanwei, Zhang, Wen, Lin, Jhih-Rong, Cai, Ying, Mitra, Joydeep, Zhang, Zhengdong D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753236/
https://www.ncbi.nlm.nih.gov/pubmed/29077884
http://dx.doi.org/10.1093/nar/gkx988
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author Wang, Zhen
Zhang, Quanwei
Zhang, Wen
Lin, Jhih-Rong
Cai, Ying
Mitra, Joydeep
Zhang, Zhengdong D
author_facet Wang, Zhen
Zhang, Quanwei
Zhang, Wen
Lin, Jhih-Rong
Cai, Ying
Mitra, Joydeep
Zhang, Zhengdong D
author_sort Wang, Zhen
collection PubMed
description Enhancers, as specialized genomic cis-regulatory elements, activate transcription of their target genes and play an important role in pathogenesis of many human complex diseases. Despite recent systematic identification of them in the human genome, currently there is an urgent need for comprehensive annotation databases of human enhancers with a focus on their disease connections. In response, we built the Human Enhancer Disease Database (HEDD) to facilitate studies of enhancers and their potential roles in human complex diseases. HEDD currently provides comprehensive genomic information for ∼2.8 million human enhancers identified by ENCODE, FANTOM5 and RoadMap with disease association scores based on enhancer–gene and gene–disease connections. It also provides Web-based analytical tools to visualize enhancer networks and score enhancers given a set of selected genes in a specific gene network. HEDD is freely accessible at http://zdzlab.einstein.yu.edu/1/hedd.php.
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spelling pubmed-57532362018-01-05 HEDD: Human Enhancer Disease Database Wang, Zhen Zhang, Quanwei Zhang, Wen Lin, Jhih-Rong Cai, Ying Mitra, Joydeep Zhang, Zhengdong D Nucleic Acids Res Database Issue Enhancers, as specialized genomic cis-regulatory elements, activate transcription of their target genes and play an important role in pathogenesis of many human complex diseases. Despite recent systematic identification of them in the human genome, currently there is an urgent need for comprehensive annotation databases of human enhancers with a focus on their disease connections. In response, we built the Human Enhancer Disease Database (HEDD) to facilitate studies of enhancers and their potential roles in human complex diseases. HEDD currently provides comprehensive genomic information for ∼2.8 million human enhancers identified by ENCODE, FANTOM5 and RoadMap with disease association scores based on enhancer–gene and gene–disease connections. It also provides Web-based analytical tools to visualize enhancer networks and score enhancers given a set of selected genes in a specific gene network. HEDD is freely accessible at http://zdzlab.einstein.yu.edu/1/hedd.php. Oxford University Press 2018-01-04 2017-10-25 /pmc/articles/PMC5753236/ /pubmed/29077884 http://dx.doi.org/10.1093/nar/gkx988 Text en Published by Oxford University Press on behalf of Nucleic Acids Research 2017. This work is written by (a) US Government employee(s) and is in the public domain in the US.
spellingShingle Database Issue
Wang, Zhen
Zhang, Quanwei
Zhang, Wen
Lin, Jhih-Rong
Cai, Ying
Mitra, Joydeep
Zhang, Zhengdong D
HEDD: Human Enhancer Disease Database
title HEDD: Human Enhancer Disease Database
title_full HEDD: Human Enhancer Disease Database
title_fullStr HEDD: Human Enhancer Disease Database
title_full_unstemmed HEDD: Human Enhancer Disease Database
title_short HEDD: Human Enhancer Disease Database
title_sort hedd: human enhancer disease database
topic Database Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753236/
https://www.ncbi.nlm.nih.gov/pubmed/29077884
http://dx.doi.org/10.1093/nar/gkx988
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