4.8 Article

LncTarD: a manually-curated database of experimentally-supported functional lncRNA-target regulations in human diseases

Journal

NUCLEIC ACIDS RESEARCH
Volume 48, Issue D1, Pages D118-D126

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkz985

Keywords

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Funding

  1. National Natural Science Foundation of China [31801115, 61803129, 61603116, 61873075]
  2. China Postdoctoral Science Foundation [2018M631943, 2018M641860]
  3. China Postdoctoral Science Special Foundation [2019T120280]
  4. Hei Long Jiang Postdoctoral Foundation [LBH-Z17110, LBH-Z17218]
  5. General Program of Natural Science Foundation of Heilongjiang Province [H2016055]
  6. Fundamental Research Funds for the Provincial Universities [2017JCZX54, 2017JCZX51]
  7. Heilongjiang Provincial Health and Family Planning Commission of Science Foundation [2018476, 2018477]
  8. Heilongjiang Provincial planning office key subjects [GBB1318066]

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Long non-coding RNAs (lncRNAs) are associated with human diseases. Although lncRNA-disease associations have received significant attention, no online repository is available to collect lncRNA-mediated regulatory mechanisms, key downstream targets, and important biological functions driven by disease-related lncRNAs in human diseases. We thus developed LncTarD (http://biocc.hrbmu.edu.cn/LncTarD/or http://bio-bigdata.hrbmu.edu.cn/LncTarD), a manually-curated database that provides a comprehensive resource of key lncRNA-target regulations, lncRNA-influenced functions, and lncRNA-mediated regulatory mechanisms in human diseases. LncTarD offers (i) 2822 key lncRNA-target regulations involving 475 lncRNAs and 1039 targets associated with 177 human diseases; (ii) 1613 experimentally-supported functional regulations and 1209 expression associations in human diseases; (iii) important biological functions driven by disease-related lncRNAs in human diseases; (iv) lncRNA-target regulations responsible for drug resistance or sensitivity in human diseases and (v) lncRNA microarray, lncRNA sequence data and transcriptome data of an 11 373 pan-cancer patient cohort from TCGA to help characterize the functional dynamics of these lncRNA-target regulations. LncTarD also provides a user-friendly interface to conveniently browse, search, and download data. LncTarD will be a useful resource platform for the further under-standing of functions and molecular mechanisms of lncRNA deregulation in human disease, which will help to identify novel and sensitive biomarkers and therapeutic targets.

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