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Lnc2Meth:一个手动整理的数据库,包含与人类疾病相关的长非编码 RNA 和 DNA 甲基化之间的调控关系。

Lnc2Meth: a manually curated database of regulatory relationships between long non-coding RNAs and DNA methylation associated with human disease.

机构信息

College of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.

Affiliation Department of Histology and Embryology, Harbin Medical University, Harbin 150081, China.

出版信息

Nucleic Acids Res. 2018 Jan 4;46(D1):D133-D138. doi: 10.1093/nar/gkx985.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de7a/5753220/54ff6c065730/gkx985fig1.jpg

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