MendelVar: gene prioritization at GWAS loci using phenotypic enrichment of Mendelian disease genes
Abstract Motivation Gene prioritization at human GWAS loci is challenging due to linkage-disequilibrium and long-range gene regulatory mechanisms. However, identifying the causal gene is crucial to enable identification of potential drug targets and better understanding of molecular mechanisms. Mapp...
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Veröffentlicht in: | Bioinformatics (Oxford, England) England), 2021-04, Vol.37 (1), p.1-8 |
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description | Abstract
Motivation
Gene prioritization at human GWAS loci is challenging due to linkage-disequilibrium and long-range gene regulatory mechanisms. However, identifying the causal gene is crucial to enable identification of potential drug targets and better understanding of molecular mechanisms. Mapping GWAS traits to known phenotypically relevant Mendelian disease genes near a locus is a promising approach to gene prioritization.
Results
We present MendelVar, a comprehensive tool that integrates knowledge from four databases on Mendelian disease genes with enrichment testing for a range of associated functional annotations such as Human Phenotype Ontology, Disease Ontology and variants from ClinVar. This open web-based platform enables users to strengthen the case for causal importance of phenotypically matched candidate genes at GWAS loci. We demonstrate the use of MendelVar in post-GWAS gene annotation for type 1 diabetes, type 2 diabetes, blood lipids and atopic dermatitis.
Availability and implementation
MendelVar is freely available at https://mendelvar.mrcieu.ac.uk
Supplementary information
Supplementary data are available at Bioinformatics online. |
doi_str_mv | 10.1093/bioinformatics/btaa1096 |
format | Article |
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Motivation
Gene prioritization at human GWAS loci is challenging due to linkage-disequilibrium and long-range gene regulatory mechanisms. However, identifying the causal gene is crucial to enable identification of potential drug targets and better understanding of molecular mechanisms. Mapping GWAS traits to known phenotypically relevant Mendelian disease genes near a locus is a promising approach to gene prioritization.
Results
We present MendelVar, a comprehensive tool that integrates knowledge from four databases on Mendelian disease genes with enrichment testing for a range of associated functional annotations such as Human Phenotype Ontology, Disease Ontology and variants from ClinVar. This open web-based platform enables users to strengthen the case for causal importance of phenotypically matched candidate genes at GWAS loci. We demonstrate the use of MendelVar in post-GWAS gene annotation for type 1 diabetes, type 2 diabetes, blood lipids and atopic dermatitis.
Availability and implementation
MendelVar is freely available at https://mendelvar.mrcieu.ac.uk
Supplementary information
Supplementary data are available at Bioinformatics online.</description><identifier>ISSN: 1367-4803</identifier><identifier>EISSN: 1367-4811</identifier><identifier>DOI: 10.1093/bioinformatics/btaa1096</identifier><identifier>PMID: 33453101</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><ispartof>Bioinformatics (Oxford, England), 2021-04, Vol.37 (1), p.1-8</ispartof><rights>The Author(s) 2021. Published by Oxford University Press. 2021</rights><rights>The Author(s) 2021. Published by Oxford University Press.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3206-835c7daf75cdc50032c5aac47e75910f559c10976e4bc99a6cab17d39c0798303</citedby><cites>FETCH-LOGICAL-c3206-835c7daf75cdc50032c5aac47e75910f559c10976e4bc99a6cab17d39c0798303</cites><orcidid>0000-0003-0000-4100</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,1586,1606,27931,27932</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33453101$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Robinson, Peter</contributor><creatorcontrib>Sobczyk, M K</creatorcontrib><creatorcontrib>Gaunt, T R</creatorcontrib><creatorcontrib>Paternoster, L</creatorcontrib><title>MendelVar: gene prioritization at GWAS loci using phenotypic enrichment of Mendelian disease genes</title><title>Bioinformatics (Oxford, England)</title><addtitle>Bioinformatics</addtitle><description>Abstract
Motivation
Gene prioritization at human GWAS loci is challenging due to linkage-disequilibrium and long-range gene regulatory mechanisms. However, identifying the causal gene is crucial to enable identification of potential drug targets and better understanding of molecular mechanisms. Mapping GWAS traits to known phenotypically relevant Mendelian disease genes near a locus is a promising approach to gene prioritization.
Results
We present MendelVar, a comprehensive tool that integrates knowledge from four databases on Mendelian disease genes with enrichment testing for a range of associated functional annotations such as Human Phenotype Ontology, Disease Ontology and variants from ClinVar. This open web-based platform enables users to strengthen the case for causal importance of phenotypically matched candidate genes at GWAS loci. We demonstrate the use of MendelVar in post-GWAS gene annotation for type 1 diabetes, type 2 diabetes, blood lipids and atopic dermatitis.
Availability and implementation
MendelVar is freely available at https://mendelvar.mrcieu.ac.uk
Supplementary information
Supplementary data are available at Bioinformatics online.</description><issn>1367-4803</issn><issn>1367-4811</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNqNkM1OwzAQhC0EoqXwCuAjl1I7juOGW1VBQSriwN8xcjab1iixg50cytMTaKnEjdOuVjPfaoaQC86uOEvFJDfO2NL5WrcGwiRvte7vyQEZcpGocTzl_HC_MzEgJyG8M8Ykk8kxGQgRS8EZH5L8AW2B1av213SFFmnjjfOmNZ892VmqW7p4mz3RyoGhXTB2RZs1WtduGgMUrTewrtG21JV0izLa0sIE1AF_iOGUHJW6Cni2myPycnvzPL8bLx8X9_PZcgwiYsl4KiSoQpdKQgGSMRGB1BpihUqmnJVSptBnVAnGOaSpTkDnXBUiBabSqWBiRC633Ma7jw5Dm9UmAFaVtui6kEWS8yhWEU96qdpKwbsQPJZZH7vWfpNxln0XnP0tOPstuHee7550eY3F3vfbaC-ItgLXNf-mfgHaMI81</recordid><startdate>20210409</startdate><enddate>20210409</enddate><creator>Sobczyk, M K</creator><creator>Gaunt, T R</creator><creator>Paternoster, L</creator><general>Oxford University Press</general><scope>TOX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0000-4100</orcidid></search><sort><creationdate>20210409</creationdate><title>MendelVar: gene prioritization at GWAS loci using phenotypic enrichment of Mendelian disease genes</title><author>Sobczyk, M K ; Gaunt, T R ; Paternoster, L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3206-835c7daf75cdc50032c5aac47e75910f559c10976e4bc99a6cab17d39c0798303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sobczyk, M K</creatorcontrib><creatorcontrib>Gaunt, T R</creatorcontrib><creatorcontrib>Paternoster, L</creatorcontrib><collection>Access via Oxford University Press (Open Access Collection)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioinformatics (Oxford, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sobczyk, M K</au><au>Gaunt, T R</au><au>Paternoster, L</au><au>Robinson, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MendelVar: gene prioritization at GWAS loci using phenotypic enrichment of Mendelian disease genes</atitle><jtitle>Bioinformatics (Oxford, England)</jtitle><addtitle>Bioinformatics</addtitle><date>2021-04-09</date><risdate>2021</risdate><volume>37</volume><issue>1</issue><spage>1</spage><epage>8</epage><pages>1-8</pages><issn>1367-4803</issn><eissn>1367-4811</eissn><abstract>Abstract
Motivation
Gene prioritization at human GWAS loci is challenging due to linkage-disequilibrium and long-range gene regulatory mechanisms. However, identifying the causal gene is crucial to enable identification of potential drug targets and better understanding of molecular mechanisms. Mapping GWAS traits to known phenotypically relevant Mendelian disease genes near a locus is a promising approach to gene prioritization.
Results
We present MendelVar, a comprehensive tool that integrates knowledge from four databases on Mendelian disease genes with enrichment testing for a range of associated functional annotations such as Human Phenotype Ontology, Disease Ontology and variants from ClinVar. This open web-based platform enables users to strengthen the case for causal importance of phenotypically matched candidate genes at GWAS loci. We demonstrate the use of MendelVar in post-GWAS gene annotation for type 1 diabetes, type 2 diabetes, blood lipids and atopic dermatitis.
Availability and implementation
MendelVar is freely available at https://mendelvar.mrcieu.ac.uk
Supplementary information
Supplementary data are available at Bioinformatics online.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>33453101</pmid><doi>10.1093/bioinformatics/btaa1096</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-0000-4100</orcidid><oa>free_for_read</oa></addata></record> |
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title | MendelVar: gene prioritization at GWAS loci using phenotypic enrichment of Mendelian disease genes |
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