Go!Poly: A gene-oriented polymorphism database
Human genome polymorphisms play a key role in defining the molecular basis of phenotypic differences between individuals in aspects such as disease susceptibility and drug responses. The database requirements for supporting the study of human genetic variation have been well recognized. In order to...
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Veröffentlicht in: | Human mutation 2001-11, Vol.18 (5), p.382-387 |
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creator | Zhang, Ge Zhang, Sizhong Chen, Wei Qiu, Weimin Wu, Hui Wang, Jianmin Luo, Jingchu Gu, Xiaocheng Cotton, Richard G.H. |
description | Human genome polymorphisms play a key role in defining the molecular basis of phenotypic differences between individuals in aspects such as disease susceptibility and drug responses. The database requirements for supporting the study of human genetic variation have been well recognized. In order to meet these needs, several generalized databases have been built. However, it is still hard for users to find gene‐related variation data from these huge and sophisticated databases. In its role as a gene‐oriented directory of polymorphism data, Go!Poly (Gene Oriented Polymorphism Database; http://61.139.84.5/gopoly/) utilizes two new highly curated and non‐redundant resources, LocusLink (http://www.ncbi.nlm.nih.gov/LocusLink/) and RefSeq (http://www.ncbi.nlm.nih.gov/LocusLink/refseq.html), as the standard for identifying and positioning nucleotide variations. As a generalized polymorphism database, Go!Poly extracts human gene‐linked sequence variations of all common types (SNP, insertion‐deletion, simple tandem repeat, and complex nucleotides variations) from various public resources including scientific journals and internet resources, such as HGBASE (http://hgbase.cgr.ki.se) and dbSNP (http://www.ncbi.nlm.nih.gov/SNP/). The polymorphism data are then categorized into different gene loci, and the reference sequences given by LocusLink are used as positioning references. Through close integration with LocusLink, Go!Poly also provides facilitated connections among sequence data, gene name, and related biological information. This feature also makes Go!Poly easy to search and navigate. Future automated annotations and internal consistency checking may also benefit from this. Extensive efforts are being taken to make the polymorphism information generated by the Chinese scientific community available from this resource. Hum Mutat 18:382–387, 2001. © 2001 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/humu.1209 |
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The database requirements for supporting the study of human genetic variation have been well recognized. In order to meet these needs, several generalized databases have been built. However, it is still hard for users to find gene‐related variation data from these huge and sophisticated databases. In its role as a gene‐oriented directory of polymorphism data, Go!Poly (Gene Oriented Polymorphism Database; http://61.139.84.5/gopoly/) utilizes two new highly curated and non‐redundant resources, LocusLink (http://www.ncbi.nlm.nih.gov/LocusLink/) and RefSeq (http://www.ncbi.nlm.nih.gov/LocusLink/refseq.html), as the standard for identifying and positioning nucleotide variations. As a generalized polymorphism database, Go!Poly extracts human gene‐linked sequence variations of all common types (SNP, insertion‐deletion, simple tandem repeat, and complex nucleotides variations) from various public resources including scientific journals and internet resources, such as HGBASE (http://hgbase.cgr.ki.se) and dbSNP (http://www.ncbi.nlm.nih.gov/SNP/). The polymorphism data are then categorized into different gene loci, and the reference sequences given by LocusLink are used as positioning references. Through close integration with LocusLink, Go!Poly also provides facilitated connections among sequence data, gene name, and related biological information. This feature also makes Go!Poly easy to search and navigate. Future automated annotations and internal consistency checking may also benefit from this. Extensive efforts are being taken to make the polymorphism information generated by the Chinese scientific community available from this resource. Hum Mutat 18:382–387, 2001. © 2001 Wiley‐Liss, Inc.</description><identifier>ISSN: 1059-7794</identifier><identifier>EISSN: 1098-1004</identifier><identifier>DOI: 10.1002/humu.1209</identifier><identifier>PMID: 11668631</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>bioinformatics ; China ; Computational Biology ; Databases, Nucleic Acid ; Genes ; Genetic Variation - genetics ; Genome, Human ; genomic analysis ; Genomics ; Humans ; Information Storage and Retrieval ; Internet ; Mutation - genetics ; polymorphism database ; Polymorphism, Genetic - genetics ; Sensitivity and Specificity ; SNP ; User-Computer Interface ; variation</subject><ispartof>Human mutation, 2001-11, Vol.18 (5), p.382-387</ispartof><rights>Copyright © 2001 Wiley‐Liss, Inc.</rights><rights>Copyright 2001 Wiley-Liss, Inc.</rights><rights>Copyright © 2001 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3819-bdab7856e0f50697b07d8016f03cd757e7c9858937462f9ab33399fd47912b8f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhumu.1209$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhumu.1209$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11668631$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Ge</creatorcontrib><creatorcontrib>Zhang, Sizhong</creatorcontrib><creatorcontrib>Chen, Wei</creatorcontrib><creatorcontrib>Qiu, Weimin</creatorcontrib><creatorcontrib>Wu, Hui</creatorcontrib><creatorcontrib>Wang, Jianmin</creatorcontrib><creatorcontrib>Luo, Jingchu</creatorcontrib><creatorcontrib>Gu, Xiaocheng</creatorcontrib><creatorcontrib>Cotton, Richard G.H.</creatorcontrib><title>Go!Poly: A gene-oriented polymorphism database</title><title>Human mutation</title><addtitle>Hum. Mutat</addtitle><description>Human genome polymorphisms play a key role in defining the molecular basis of phenotypic differences between individuals in aspects such as disease susceptibility and drug responses. The database requirements for supporting the study of human genetic variation have been well recognized. In order to meet these needs, several generalized databases have been built. However, it is still hard for users to find gene‐related variation data from these huge and sophisticated databases. In its role as a gene‐oriented directory of polymorphism data, Go!Poly (Gene Oriented Polymorphism Database; http://61.139.84.5/gopoly/) utilizes two new highly curated and non‐redundant resources, LocusLink (http://www.ncbi.nlm.nih.gov/LocusLink/) and RefSeq (http://www.ncbi.nlm.nih.gov/LocusLink/refseq.html), as the standard for identifying and positioning nucleotide variations. As a generalized polymorphism database, Go!Poly extracts human gene‐linked sequence variations of all common types (SNP, insertion‐deletion, simple tandem repeat, and complex nucleotides variations) from various public resources including scientific journals and internet resources, such as HGBASE (http://hgbase.cgr.ki.se) and dbSNP (http://www.ncbi.nlm.nih.gov/SNP/). The polymorphism data are then categorized into different gene loci, and the reference sequences given by LocusLink are used as positioning references. Through close integration with LocusLink, Go!Poly also provides facilitated connections among sequence data, gene name, and related biological information. This feature also makes Go!Poly easy to search and navigate. Future automated annotations and internal consistency checking may also benefit from this. Extensive efforts are being taken to make the polymorphism information generated by the Chinese scientific community available from this resource. Hum Mutat 18:382–387, 2001. © 2001 Wiley‐Liss, Inc.</description><subject>bioinformatics</subject><subject>China</subject><subject>Computational Biology</subject><subject>Databases, Nucleic Acid</subject><subject>Genes</subject><subject>Genetic Variation - genetics</subject><subject>Genome, Human</subject><subject>genomic analysis</subject><subject>Genomics</subject><subject>Humans</subject><subject>Information Storage and Retrieval</subject><subject>Internet</subject><subject>Mutation - genetics</subject><subject>polymorphism database</subject><subject>Polymorphism, Genetic - genetics</subject><subject>Sensitivity and Specificity</subject><subject>SNP</subject><subject>User-Computer Interface</subject><subject>variation</subject><issn>1059-7794</issn><issn>1098-1004</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kE1Lw0AURQdRrFYX_gGJLgQXaWcymS93tWor1OrCorthkkxsar6cSdD-exMSFARX7_E49_I4AJwgOEIQeuN1ndUj5EGxAw4QFNxtrv5uuxPhMib8ATi0dgMh5ITgfTBAiFJOMToAo1lx9lSk2ytn4rzpXLuFSXRe6cgpm2tWmHKd2MyJVKUCZfUR2ItVavVxP4dgdXf7PJ27i8fZ_XSycEPMkXCDSAWME6phTCAVLIAs4hDRGOIwYoRpFgpOuMDMp14sVIAxFiKOfCaQF_AYD8FF11ua4qPWtpJZYkOdpirXRW0l8zwkCBMNeP4H3BS1yZvfJBLM41gQ2kCXHRSawlqjY1maJFNmKxGUrUHZGpStwYY97QvrINPRL9kra4BxB3wmqd7-3yTnq4dVX-l2icRW-usnocy7pAwzIl-WM-nBV359s8TSx9-BK4cv</recordid><startdate>200111</startdate><enddate>200111</enddate><creator>Zhang, Ge</creator><creator>Zhang, Sizhong</creator><creator>Chen, Wei</creator><creator>Qiu, Weimin</creator><creator>Wu, Hui</creator><creator>Wang, Jianmin</creator><creator>Luo, Jingchu</creator><creator>Gu, Xiaocheng</creator><creator>Cotton, Richard G.H.</creator><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200111</creationdate><title>Go!Poly: A gene-oriented polymorphism database</title><author>Zhang, Ge ; Zhang, Sizhong ; Chen, Wei ; Qiu, Weimin ; Wu, Hui ; Wang, Jianmin ; Luo, Jingchu ; Gu, Xiaocheng ; Cotton, Richard G.H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3819-bdab7856e0f50697b07d8016f03cd757e7c9858937462f9ab33399fd47912b8f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>bioinformatics</topic><topic>China</topic><topic>Computational Biology</topic><topic>Databases, Nucleic Acid</topic><topic>Genes</topic><topic>Genetic Variation - genetics</topic><topic>Genome, Human</topic><topic>genomic analysis</topic><topic>Genomics</topic><topic>Humans</topic><topic>Information Storage and Retrieval</topic><topic>Internet</topic><topic>Mutation - genetics</topic><topic>polymorphism database</topic><topic>Polymorphism, Genetic - genetics</topic><topic>Sensitivity and Specificity</topic><topic>SNP</topic><topic>User-Computer Interface</topic><topic>variation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Ge</creatorcontrib><creatorcontrib>Zhang, Sizhong</creatorcontrib><creatorcontrib>Chen, Wei</creatorcontrib><creatorcontrib>Qiu, Weimin</creatorcontrib><creatorcontrib>Wu, Hui</creatorcontrib><creatorcontrib>Wang, Jianmin</creatorcontrib><creatorcontrib>Luo, Jingchu</creatorcontrib><creatorcontrib>Gu, Xiaocheng</creatorcontrib><creatorcontrib>Cotton, Richard G.H.</creatorcontrib><collection>Istex</collection><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>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech 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>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</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>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Human mutation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Ge</au><au>Zhang, Sizhong</au><au>Chen, Wei</au><au>Qiu, Weimin</au><au>Wu, Hui</au><au>Wang, Jianmin</au><au>Luo, Jingchu</au><au>Gu, Xiaocheng</au><au>Cotton, Richard G.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Go!Poly: A gene-oriented polymorphism database</atitle><jtitle>Human mutation</jtitle><addtitle>Hum. Mutat</addtitle><date>2001-11</date><risdate>2001</risdate><volume>18</volume><issue>5</issue><spage>382</spage><epage>387</epage><pages>382-387</pages><issn>1059-7794</issn><eissn>1098-1004</eissn><abstract>Human genome polymorphisms play a key role in defining the molecular basis of phenotypic differences between individuals in aspects such as disease susceptibility and drug responses. The database requirements for supporting the study of human genetic variation have been well recognized. In order to meet these needs, several generalized databases have been built. However, it is still hard for users to find gene‐related variation data from these huge and sophisticated databases. In its role as a gene‐oriented directory of polymorphism data, Go!Poly (Gene Oriented Polymorphism Database; http://61.139.84.5/gopoly/) utilizes two new highly curated and non‐redundant resources, LocusLink (http://www.ncbi.nlm.nih.gov/LocusLink/) and RefSeq (http://www.ncbi.nlm.nih.gov/LocusLink/refseq.html), as the standard for identifying and positioning nucleotide variations. As a generalized polymorphism database, Go!Poly extracts human gene‐linked sequence variations of all common types (SNP, insertion‐deletion, simple tandem repeat, and complex nucleotides variations) from various public resources including scientific journals and internet resources, such as HGBASE (http://hgbase.cgr.ki.se) and dbSNP (http://www.ncbi.nlm.nih.gov/SNP/). The polymorphism data are then categorized into different gene loci, and the reference sequences given by LocusLink are used as positioning references. Through close integration with LocusLink, Go!Poly also provides facilitated connections among sequence data, gene name, and related biological information. This feature also makes Go!Poly easy to search and navigate. Future automated annotations and internal consistency checking may also benefit from this. Extensive efforts are being taken to make the polymorphism information generated by the Chinese scientific community available from this resource. Hum Mutat 18:382–387, 2001. © 2001 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>11668631</pmid><doi>10.1002/humu.1209</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | bioinformatics China Computational Biology Databases, Nucleic Acid Genes Genetic Variation - genetics Genome, Human genomic analysis Genomics Humans Information Storage and Retrieval Internet Mutation - genetics polymorphism database Polymorphism, Genetic - genetics Sensitivity and Specificity SNP User-Computer Interface variation |
title | Go!Poly: A gene-oriented polymorphism database |
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