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首页> 外文期刊>BioMed research international >TF2LncRNA: Identifying Common Transcription Factors for a List of lncRNA Genes from ChlP-Seq Data
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TF2LncRNA: Identifying Common Transcription Factors for a List of lncRNA Genes from ChlP-Seq Data

机译:TF2LncRNA:从ChlP-Seq数据中识别lncRNA基因列表的常见转录因子

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摘要

High-throughput genomic technologies like lncRNA microarray and RNA-Seq often generate a set of lncRNAs of interest, yet little is known about the transcriptional regulation of the set of lncRNA genes. Here, based on ChlP-Seq peak lists of transcription factors (TFs) from ENCODE and annotated human lncRNAs from GENCODE, we developed a web-based interface titled "TF2lncRNA," where TF peaks from each ChlP-Seq experiment are crossed with the genomic coordinates of a set of input lncRNAs, to identify which TFs present a statistically significant number of binding sites (peaks) within the regulatory region of the input lncRNA genes. The input can be a set of coexpressed lncRNA genes or any other cluster of lncRNA genes. Users can thus infer which TFs are likely to be common transcription regulators of the set of lncRNAs. In addition, users can retrieve all lncRNAs potentially regulated by a specific TF in a specific cell line of interest or retrieve all TFs that have one or more binding sites in the regulatory region of a given lncRNA in the specific cell line. TF2LncRNA is an efficient and easy-to-use web-based tool.
机译:诸如lncRNA芯片和RNA-Seq之类的高通量基因组技术通常会生成一组感兴趣的lncRNA,但对这套lncRNA基因的转录调控知之甚少。在此,根据来自ENCODE的转录因子(TF)的ChlP-Seq峰列表和来自GENCODE的带注释的人lncRNA,我们开发了一个基于网络的界面,名为“ TF2lncRNA”,其中每个ChlP-Seq实验的TF峰都与基因组交叉一组输入lncRNA的坐标,以识别哪些TF在输入lncRNA基因的调控区域内呈现统计学上显着数量的结合位点(峰)。输入可以是一组共表达的lncRNA基因或lncRNA基因的任何其他簇。用户因此可以推断哪些TF可能是lncRNA集合中的常见转录调节因子。另外,用户可以检索感兴趣的特定细胞系中可能由特定TF调控的所有lncRNA,或检索在特定细胞系中给定lncRNA的调控区域中具有一个或多个结合位点的所有TF。 TF2LncRNA是一种高效且易于使用的基于Web的工具。

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