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lncRNASNP2: an updated database of functional SNPs and mutations in human and mouse lncRNAs
Long non-coding RNAs (lncRNAs) are emerging as important regulators in different biological processes through various ways. Because the related data, especially mutations in cancers, increased sharply, we updated the lncRNASNP to version 2 (http://bioinfo.life.hust.edu.cn/lncRNASNP2). lncRNASNP2 pro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753387/ https://www.ncbi.nlm.nih.gov/pubmed/29077939 http://dx.doi.org/10.1093/nar/gkx1004 |
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author | Miao, Ya-Ru Liu, Wei Zhang, Qiong Guo, An-Yuan |
author_facet | Miao, Ya-Ru Liu, Wei Zhang, Qiong Guo, An-Yuan |
author_sort | Miao, Ya-Ru |
collection | PubMed |
description | Long non-coding RNAs (lncRNAs) are emerging as important regulators in different biological processes through various ways. Because the related data, especially mutations in cancers, increased sharply, we updated the lncRNASNP to version 2 (http://bioinfo.life.hust.edu.cn/lncRNASNP2). lncRNASNP2 provides comprehensive information of SNPs and mutations in lncRNAs, as well as their impacts on lncRNA structure and function. lncRNASNP2 contains 7260238 SNPs on 141353 human lncRNA transcripts and 3921448 SNPs on 117405 mouse lncRNA transcripts. Besides the SNP information in the first version, the following new features were developed to improve the lncRNASNP2. (i) noncoding variants from COSMIC cancer data (859534) in lncRNAs and their effects on lncRNA structure and function; (ii) TCGA cancer mutations (315234) in lncRNAs and their impacts; (iii) lncRNA expression profiling of 20 cancer types in both tumor and its adjacent samples; (iv) expanded lncRNA-associated diseases; (v) optimized the results about lncRNAs structure change induced by variants; (vi) reduced false positives in miRNA and lncRNA interaction results. Furthermore, we developed online tools for users to analyze new variants in lncRNA. We aim to maintain the lncRNASNP as a useful resource for lncRNAs and their variants. |
format | Online Article Text |
id | pubmed-5753387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57533872018-01-05 lncRNASNP2: an updated database of functional SNPs and mutations in human and mouse lncRNAs Miao, Ya-Ru Liu, Wei Zhang, Qiong Guo, An-Yuan Nucleic Acids Res Database Issue Long non-coding RNAs (lncRNAs) are emerging as important regulators in different biological processes through various ways. Because the related data, especially mutations in cancers, increased sharply, we updated the lncRNASNP to version 2 (http://bioinfo.life.hust.edu.cn/lncRNASNP2). lncRNASNP2 provides comprehensive information of SNPs and mutations in lncRNAs, as well as their impacts on lncRNA structure and function. lncRNASNP2 contains 7260238 SNPs on 141353 human lncRNA transcripts and 3921448 SNPs on 117405 mouse lncRNA transcripts. Besides the SNP information in the first version, the following new features were developed to improve the lncRNASNP2. (i) noncoding variants from COSMIC cancer data (859534) in lncRNAs and their effects on lncRNA structure and function; (ii) TCGA cancer mutations (315234) in lncRNAs and their impacts; (iii) lncRNA expression profiling of 20 cancer types in both tumor and its adjacent samples; (iv) expanded lncRNA-associated diseases; (v) optimized the results about lncRNAs structure change induced by variants; (vi) reduced false positives in miRNA and lncRNA interaction results. Furthermore, we developed online tools for users to analyze new variants in lncRNA. We aim to maintain the lncRNASNP as a useful resource for lncRNAs and their variants. Oxford University Press 2018-01-04 2017-10-25 /pmc/articles/PMC5753387/ /pubmed/29077939 http://dx.doi.org/10.1093/nar/gkx1004 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Database Issue Miao, Ya-Ru Liu, Wei Zhang, Qiong Guo, An-Yuan lncRNASNP2: an updated database of functional SNPs and mutations in human and mouse lncRNAs |
title | lncRNASNP2: an updated database of functional SNPs and mutations in human and mouse lncRNAs |
title_full | lncRNASNP2: an updated database of functional SNPs and mutations in human and mouse lncRNAs |
title_fullStr | lncRNASNP2: an updated database of functional SNPs and mutations in human and mouse lncRNAs |
title_full_unstemmed | lncRNASNP2: an updated database of functional SNPs and mutations in human and mouse lncRNAs |
title_short | lncRNASNP2: an updated database of functional SNPs and mutations in human and mouse lncRNAs |
title_sort | lncrnasnp2: an updated database of functional snps and mutations in human and mouse lncrnas |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753387/ https://www.ncbi.nlm.nih.gov/pubmed/29077939 http://dx.doi.org/10.1093/nar/gkx1004 |
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