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ceRNA: 用于鉴定和分析 ceRNA-miRNA 三链体的 R 包。

ceRNAR: An R package for identification and analysis of ceRNA-miRNA triplets.

机构信息

Institute of Epidemiology and Preventive Medicine, Department of Public Health, College of Public Health, National Taiwan University, Taipei, Taiwan.

Bioinformatics and Biostatistics Core, Center of Genomic and Precision Medicine, National Taiwan University, Taipei, Taiwan.

出版信息

PLoS Comput Biol. 2022 Sep 9;18(9):e1010497. doi: 10.1371/journal.pcbi.1010497. eCollection 2022 Sep.

Abstract

Competitive endogenous RNA (ceRNA) represents a novel mechanism of gene regulation that controls several biological and pathological processes. Recently, an increasing number of in silico methods have been developed to accelerate the identification of such regulatory events. However, there is still a need for a tool supporting the hypothesis that ceRNA regulatory events only occur at specific miRNA expression levels. To this end, we present an R package, ceRNAR, which allows identification and analysis of ceRNA-miRNA triplets via integration of miRNA and RNA expression data. The ceRNAR package integrates three main steps: (i) identification of ceRNA pairs based on a rank-based correlation between pairs that considers the impact of miRNA and a running sum correlation statistic, (ii) sample clustering based on gene-gene correlation by circular binary segmentation, and (iii) peak merging to identify the most relevant sample patterns. In addition, ceRNAR also provides downstream analyses of identified ceRNA-miRNA triplets, including network analysis, functional annotation, survival analysis, external validation, and integration of different tools. The performance of our proposed approach was validated through simulation studies of different scenarios. Compared with several published tools, ceRNAR was able to identify true ceRNA triplets with high sensitivity, low false-positive rates, and acceptable running time. In real data applications, the ceRNAs common to two lung cancer datasets were identified in both datasets. The bridging miRNA for one of these, the ceRNA for MAP4K3, was identified by ceRNAR as hsa-let-7c-5p. Since similar cancer subtypes do share some biological patterns, these results demonstrated that our proposed algorithm was able to identify potential ceRNA targets in real patients. In summary, ceRNAR offers a novel algorithm and a comprehensive pipeline to identify and analyze ceRNA regulation. The package is implemented in R and is available on GitHub (https://github.com/ywhsiao/ceRNAR).

摘要

竞争性内源 RNA (ceRNA) 代表了一种新的基因调控机制,可控制多种生物学和病理学过程。最近,越来越多的计算方法被开发出来,以加速这些调控事件的识别。然而,仍然需要有一种工具来支持 ceRNA 调控事件仅在特定 miRNA 表达水平发生的假设。为此,我们提出了一个 R 包 ceRNAR,它允许通过整合 miRNA 和 RNA 表达数据来识别和分析 ceRNA-miRNA 三螺旋体。ceRNAR 包集成了三个主要步骤:(i)基于 miRNA 对和运行和相关统计的影响考虑的对之间的基于秩的相关性,识别 ceRNA 对;(ii)通过循环二进制分割基于基因-基因相关性对样本进行聚类;(iii)峰合并,以识别最相关的样本模式。此外,ceRNAR 还提供了对鉴定出的 ceRNA-miRNA 三螺旋体的下游分析,包括网络分析、功能注释、生存分析、外部验证和不同工具的整合。通过不同场景的模拟研究验证了我们提出的方法的性能。与几种已发表的工具相比,ceRNAR 能够以高灵敏度、低假阳性率和可接受的运行时间识别真正的 ceRNA 三螺旋体。在真实数据应用中,在两个肺癌数据集中共鉴定出了两个数据集共有的 ceRNA。对于其中之一 MAP4K3 的 ceRNA,ceRNAR 鉴定出的桥接 miRNA 是 hsa-let-7c-5p。由于类似的癌症亚型确实存在一些共同的生物学模式,这些结果表明我们提出的算法能够在真实患者中识别潜在的 ceRNA 靶标。总之,ceRNAR 提供了一种新的算法和一个全面的管道来识别和分析 ceRNA 调控。该包用 R 实现,并可在 GitHub 上获得 (https://github.com/ywhsiao/ceRNAR)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7df8/9491567/b268edb8d338/pcbi.1010497.g001.jpg

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