College of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Affiliation Department of Histology and Embryology, Harbin Medical University, Harbin 150081, China.
Nucleic Acids Res. 2018 Jan 4;46(D1):D133-D138. doi: 10.1093/nar/gkx985.
Lnc2Meth (http://www.bio-bigdata.com/Lnc2Meth/), an interactive resource to identify regulatory relationships between human long non-coding RNAs (lncRNAs) and DNA methylation, is not only a manually curated collection and annotation of experimentally supported lncRNAs-DNA methylation associations but also a platform that effectively integrates tools for calculating and identifying the differentially methylated lncRNAs and protein-coding genes (PCGs) in diverse human diseases. The resource provides: (i) advanced search possibilities, e.g. retrieval of the database by searching the lncRNA symbol of interest, DNA methylation patterns, regulatory mechanisms and disease types; (ii) abundant computationally calculated DNA methylation array profiles for the lncRNAs and PCGs; (iii) the prognostic values for each hit transcript calculated from the patients clinical data; (iv) a genome browser to display the DNA methylation landscape of the lncRNA transcripts for a specific type of disease; (v) tools to re-annotate probes to lncRNA loci and identify the differential methylation patterns for lncRNAs and PCGs with user-supplied external datasets; (vi) an R package (LncDM) to complete the differentially methylated lncRNAs identification and visualization with local computers. Lnc2Meth provides a timely and valuable resource that can be applied to significantly expand our understanding of the regulatory relationships between lncRNAs and DNA methylation in various human diseases.
Lnc2Meth(http://www.bio-bigdata.com/Lnc2Meth/)是一个交互式资源,用于识别人类长非编码 RNA(lncRNA)与 DNA 甲基化之间的调控关系,它不仅是一个手动整理和注释实验支持的 lncRNA-DNA 甲基化关联的集合,还是一个有效整合了计算和识别差异甲基化 lncRNA 和蛋白编码基因(PCG)的工具的平台,适用于多种人类疾病。该资源提供:(i)高级搜索功能,例如通过搜索感兴趣的 lncRNA 符号、DNA 甲基化模式、调控机制和疾病类型来检索数据库;(ii)丰富的计算 DNA 甲基化阵列图谱,用于 lncRNA 和 PCG;(iii)根据患者的临床数据计算出每个命中转录本的预后值;(iv)基因组浏览器,用于显示特定疾病类型的 lncRNA 转录本的 DNA 甲基化景观;(v)工具,用于将探针重新注释到 lncRNA 基因座,并使用用户提供的外部数据集识别 lncRNA 和 PCG 的差异甲基化模式;(vi)一个 R 包(LncDM),用于使用本地计算机完成差异甲基化 lncRNA 的识别和可视化。Lnc2Meth 提供了一个及时且有价值的资源,可以应用于极大地扩展我们对各种人类疾病中 lncRNA 和 DNA 甲基化之间调控关系的理解。