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Lnc2Cancer v2.0: updated database of experimentally supported long non-coding RNAs in human cancers
Abstract Lnc2Cancer 2.0 (http://www.bio-bigdata.net/lnc2cancer) is an updated database that provides comprehensive experimentally supported associations between lncRNAs and human cancers. In Lnc2Cancer 2.0, we have updated the database with more data and several new features, including (i) exceeding...
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Published in: | Nucleic acids research 2019-01, Vol.47 (D1), p.D1028-D1033 |
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container_end_page | D1033 |
container_issue | D1 |
container_start_page | D1028 |
container_title | Nucleic acids research |
container_volume | 47 |
creator | Gao, Yue Wang, Peng Wang, Yanxia Ma, Xueyan Zhi, Hui Zhou, Dianshuang Li, Xin Fang, Ying Shen, Weitao Xu, Yingqi Shang, Shipeng Wang, Lihua Wang, Li Ning, Shangwei Li, Xia |
description | Abstract
Lnc2Cancer 2.0 (http://www.bio-bigdata.net/lnc2cancer) is an updated database that provides comprehensive experimentally supported associations between lncRNAs and human cancers. In Lnc2Cancer 2.0, we have updated the database with more data and several new features, including (i) exceeding a 4-fold increase over the previous version, recruiting 4989 lncRNA-cancer associations between 1614 lncRNAs and 165 cancer subtypes. (ii) newly adding about 800 experimentally supported circulating, drug-resistant and prognostic-related lncRNAs in various cancers. (iii) appending the regulatory mechanism of lncRNA in cancer, including microRNA (miRNA), transcription factor (TF), variant and methylation regulation. (iv) increasing more than 70 high-throughput experiments (microarray and next-generation sequencing) of lncRNAs in cancers. (v) Scoring the associations between lncRNA and cancer to evaluate the correlations. (vi) updating the annotation information of lncRNAs (version 28) and containing more detailed descriptions for lncRNAs and cancers. Moreover, a newly designed, user-friendly interface was also developed to provide a convenient platform for users. In particular, the functions of browsing data by cancer primary organ, biomarker type and regulatory mechanism, advanced search following several features and filtering the data by LncRNA-Cancer score were enhanced. Lnc2Cancer 2.0 will be a useful resource platform for further understanding the associations between lncRNA and human cancer. |
doi_str_mv | 10.1093/nar/gky1096 |
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Lnc2Cancer 2.0 (http://www.bio-bigdata.net/lnc2cancer) is an updated database that provides comprehensive experimentally supported associations between lncRNAs and human cancers. In Lnc2Cancer 2.0, we have updated the database with more data and several new features, including (i) exceeding a 4-fold increase over the previous version, recruiting 4989 lncRNA-cancer associations between 1614 lncRNAs and 165 cancer subtypes. (ii) newly adding about 800 experimentally supported circulating, drug-resistant and prognostic-related lncRNAs in various cancers. (iii) appending the regulatory mechanism of lncRNA in cancer, including microRNA (miRNA), transcription factor (TF), variant and methylation regulation. (iv) increasing more than 70 high-throughput experiments (microarray and next-generation sequencing) of lncRNAs in cancers. (v) Scoring the associations between lncRNA and cancer to evaluate the correlations. (vi) updating the annotation information of lncRNAs (version 28) and containing more detailed descriptions for lncRNAs and cancers. Moreover, a newly designed, user-friendly interface was also developed to provide a convenient platform for users. In particular, the functions of browsing data by cancer primary organ, biomarker type and regulatory mechanism, advanced search following several features and filtering the data by LncRNA-Cancer score were enhanced. Lnc2Cancer 2.0 will be a useful resource platform for further understanding the associations between lncRNA and human cancer.</description><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/gky1096</identifier><identifier>PMID: 30407549</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Data Management - methods ; Database Issue ; Databases, Genetic ; Gene Expression Regulation, Neoplastic ; Humans ; Internet ; MicroRNAs - genetics ; Neoplasms - classification ; Neoplasms - diagnosis ; Neoplasms - genetics ; RNA, Long Noncoding - genetics ; Software ; Transcription Factors - genetics</subject><ispartof>Nucleic acids research, 2019-01, Vol.47 (D1), p.D1028-D1033</ispartof><rights>The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-9f76765b6e89677601da41cc0d835ab6f48ff2f619ac0b9938e325c9b589b6bb3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324001/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324001/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,1604,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30407549$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gao, Yue</creatorcontrib><creatorcontrib>Wang, Peng</creatorcontrib><creatorcontrib>Wang, Yanxia</creatorcontrib><creatorcontrib>Ma, Xueyan</creatorcontrib><creatorcontrib>Zhi, Hui</creatorcontrib><creatorcontrib>Zhou, Dianshuang</creatorcontrib><creatorcontrib>Li, Xin</creatorcontrib><creatorcontrib>Fang, Ying</creatorcontrib><creatorcontrib>Shen, Weitao</creatorcontrib><creatorcontrib>Xu, Yingqi</creatorcontrib><creatorcontrib>Shang, Shipeng</creatorcontrib><creatorcontrib>Wang, Lihua</creatorcontrib><creatorcontrib>Wang, Li</creatorcontrib><creatorcontrib>Ning, Shangwei</creatorcontrib><creatorcontrib>Li, Xia</creatorcontrib><title>Lnc2Cancer v2.0: updated database of experimentally supported long non-coding RNAs in human cancers</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><description>Abstract
Lnc2Cancer 2.0 (http://www.bio-bigdata.net/lnc2cancer) is an updated database that provides comprehensive experimentally supported associations between lncRNAs and human cancers. In Lnc2Cancer 2.0, we have updated the database with more data and several new features, including (i) exceeding a 4-fold increase over the previous version, recruiting 4989 lncRNA-cancer associations between 1614 lncRNAs and 165 cancer subtypes. (ii) newly adding about 800 experimentally supported circulating, drug-resistant and prognostic-related lncRNAs in various cancers. (iii) appending the regulatory mechanism of lncRNA in cancer, including microRNA (miRNA), transcription factor (TF), variant and methylation regulation. (iv) increasing more than 70 high-throughput experiments (microarray and next-generation sequencing) of lncRNAs in cancers. (v) Scoring the associations between lncRNA and cancer to evaluate the correlations. (vi) updating the annotation information of lncRNAs (version 28) and containing more detailed descriptions for lncRNAs and cancers. Moreover, a newly designed, user-friendly interface was also developed to provide a convenient platform for users. In particular, the functions of browsing data by cancer primary organ, biomarker type and regulatory mechanism, advanced search following several features and filtering the data by LncRNA-Cancer score were enhanced. Lnc2Cancer 2.0 will be a useful resource platform for further understanding the associations between lncRNA and human cancer.</description><subject>Data Management - methods</subject><subject>Database Issue</subject><subject>Databases, Genetic</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Internet</subject><subject>MicroRNAs - genetics</subject><subject>Neoplasms - classification</subject><subject>Neoplasms - diagnosis</subject><subject>Neoplasms - genetics</subject><subject>RNA, Long Noncoding - genetics</subject><subject>Software</subject><subject>Transcription Factors - genetics</subject><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNp9kUtLAzEURoMoWh8r95KVCDI2r8lMXAil-IKiILoOSSZTR6fJmHTE_ntTW0U3bpILOZx83A-AQ4zOMBJ06FQYTl8XaeYbYIApJxkTnGyCAaIozzBi5Q7YjfEFIcxwzrbBDkUMFTkTA2AmzpCxcsYG-E7O0Dnsu0rNbQXTqbSKFvoa2o_OhmZm3Vy17QLGvut8WEKtd1PovMuMr5o0PtyNImwcfO5nykHz5Y37YKtWbbQH63sPPF1dPo5vssn99e14NMkMK8p5JuqCFzzX3JaCFwVHuFIMG4OqkuZK85qVdU1qjoUySAtBS0tJboTOS6G51nQPXKy8Xa9ntjIpblCt7FJyFRbSq0b-fXHNs5z6d8kpYWk5SXCyFgT_1ts4l7MmGtu2ylnfR0kwxYRywUVCT1eoCT7GYOufbzCSy1pkqkWua0n00e9kP-x3Dwk4XgG-7_41fQIAJ5eX</recordid><startdate>20190108</startdate><enddate>20190108</enddate><creator>Gao, Yue</creator><creator>Wang, Peng</creator><creator>Wang, Yanxia</creator><creator>Ma, Xueyan</creator><creator>Zhi, Hui</creator><creator>Zhou, Dianshuang</creator><creator>Li, Xin</creator><creator>Fang, Ying</creator><creator>Shen, Weitao</creator><creator>Xu, Yingqi</creator><creator>Shang, Shipeng</creator><creator>Wang, Lihua</creator><creator>Wang, Li</creator><creator>Ning, Shangwei</creator><creator>Li, Xia</creator><general>Oxford University Press</general><scope>TOX</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190108</creationdate><title>Lnc2Cancer v2.0: updated database of experimentally supported long non-coding RNAs in human cancers</title><author>Gao, Yue ; Wang, Peng ; Wang, Yanxia ; Ma, Xueyan ; Zhi, Hui ; Zhou, Dianshuang ; Li, Xin ; Fang, Ying ; Shen, Weitao ; Xu, Yingqi ; Shang, Shipeng ; Wang, Lihua ; Wang, Li ; Ning, Shangwei ; Li, Xia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-9f76765b6e89677601da41cc0d835ab6f48ff2f619ac0b9938e325c9b589b6bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Data Management - methods</topic><topic>Database Issue</topic><topic>Databases, Genetic</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Internet</topic><topic>MicroRNAs - genetics</topic><topic>Neoplasms - classification</topic><topic>Neoplasms - diagnosis</topic><topic>Neoplasms - genetics</topic><topic>RNA, Long Noncoding - genetics</topic><topic>Software</topic><topic>Transcription Factors - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Yue</creatorcontrib><creatorcontrib>Wang, Peng</creatorcontrib><creatorcontrib>Wang, Yanxia</creatorcontrib><creatorcontrib>Ma, Xueyan</creatorcontrib><creatorcontrib>Zhi, Hui</creatorcontrib><creatorcontrib>Zhou, Dianshuang</creatorcontrib><creatorcontrib>Li, Xin</creatorcontrib><creatorcontrib>Fang, Ying</creatorcontrib><creatorcontrib>Shen, Weitao</creatorcontrib><creatorcontrib>Xu, Yingqi</creatorcontrib><creatorcontrib>Shang, Shipeng</creatorcontrib><creatorcontrib>Wang, Lihua</creatorcontrib><creatorcontrib>Wang, Li</creatorcontrib><creatorcontrib>Ning, Shangwei</creatorcontrib><creatorcontrib>Li, Xia</creatorcontrib><collection>Oxford Academic Journals (Open Access)</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gao, Yue</au><au>Wang, Peng</au><au>Wang, Yanxia</au><au>Ma, Xueyan</au><au>Zhi, Hui</au><au>Zhou, Dianshuang</au><au>Li, Xin</au><au>Fang, Ying</au><au>Shen, Weitao</au><au>Xu, Yingqi</au><au>Shang, Shipeng</au><au>Wang, Lihua</au><au>Wang, Li</au><au>Ning, Shangwei</au><au>Li, Xia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lnc2Cancer v2.0: updated database of experimentally supported long non-coding RNAs in human cancers</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2019-01-08</date><risdate>2019</risdate><volume>47</volume><issue>D1</issue><spage>D1028</spage><epage>D1033</epage><pages>D1028-D1033</pages><issn>0305-1048</issn><eissn>1362-4962</eissn><abstract>Abstract
Lnc2Cancer 2.0 (http://www.bio-bigdata.net/lnc2cancer) is an updated database that provides comprehensive experimentally supported associations between lncRNAs and human cancers. In Lnc2Cancer 2.0, we have updated the database with more data and several new features, including (i) exceeding a 4-fold increase over the previous version, recruiting 4989 lncRNA-cancer associations between 1614 lncRNAs and 165 cancer subtypes. (ii) newly adding about 800 experimentally supported circulating, drug-resistant and prognostic-related lncRNAs in various cancers. (iii) appending the regulatory mechanism of lncRNA in cancer, including microRNA (miRNA), transcription factor (TF), variant and methylation regulation. (iv) increasing more than 70 high-throughput experiments (microarray and next-generation sequencing) of lncRNAs in cancers. (v) Scoring the associations between lncRNA and cancer to evaluate the correlations. (vi) updating the annotation information of lncRNAs (version 28) and containing more detailed descriptions for lncRNAs and cancers. Moreover, a newly designed, user-friendly interface was also developed to provide a convenient platform for users. In particular, the functions of browsing data by cancer primary organ, biomarker type and regulatory mechanism, advanced search following several features and filtering the data by LncRNA-Cancer score were enhanced. Lnc2Cancer 2.0 will be a useful resource platform for further understanding the associations between lncRNA and human cancer.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>30407549</pmid><doi>10.1093/nar/gky1096</doi><oa>free_for_read</oa></addata></record> |
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subjects | Data Management - methods Database Issue Databases, Genetic Gene Expression Regulation, Neoplastic Humans Internet MicroRNAs - genetics Neoplasms - classification Neoplasms - diagnosis Neoplasms - genetics RNA, Long Noncoding - genetics Software Transcription Factors - genetics |
title | Lnc2Cancer v2.0: updated database of experimentally supported long non-coding RNAs in human cancers |
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