Departamento de Bioquímica, Universidad Autónoma de Madrid (UAM) and Instituto de Investigaciones Biomédicas 'Alberto Sols' (CSIC-UAM), Madrid, Spain.
Department of Medical Genetics, University of British Columbia Vancouver, Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, Vancouver, BC V5Z 4H4, Canada.
Bioinformatics. 2019 Dec 15;35(24):5339-5340. doi: 10.1093/bioinformatics/btz573.
The computational identification of the transcription factors (TFs) [more generally, transcription regulators, (TR)] responsible for the co-regulation of a specific set of genes is a common problem found in genomic analysis. Herein, we describe TFEA.ChIP, a tool that makes use of ChIP-seq datasets to estimate and visualize TR enrichment in gene lists representing transcriptional profiles. We validated TFEA.ChIP using a wide variety of gene sets representing signatures of genetic and chemical perturbations as input and found that the relevant TR was correctly identified in 126 of a total of 174 analyzed. Comparison with other TR enrichment tools demonstrates that TFEA.ChIP is an highly customizable package with an outstanding performance.
TFEA.ChIP is implemented as an R package available at Bioconductor https://www.bioconductor.org/packages/devel/bioc/html/TFEA.ChIP.html and github https://github.com/LauraPS1/TFEA.ChIP_downloads. A web-based GUI to the package is also available at https://www.iib.uam.es/TFEA.ChIP/.
Supplementary data are available at Bioinformatics online.
在基因组分析中,鉴定负责特定基因集协同调控的转录因子(TFs)[更一般地说,转录调节剂(TR)]是一个常见的问题。本文中,我们描述了 TFEA.ChIP,这是一种利用 ChIP-seq 数据集来估计和可视化代表转录谱的基因列表中 TR 富集的工具。我们使用多种代表遗传和化学扰动特征的基因集作为输入来验证 TFEA.ChIP,发现总共分析的 174 个中有 126 个正确识别了相关的 TR。与其他 TR 富集工具的比较表明,TFEA.ChIP 是一个高度可定制的包,具有出色的性能。
TFEA.ChIP 作为一个 R 包实现,可在 Bioconductor https://www.bioconductor.org/packages/devel/bioc/html/TFEA.ChIP.html 和 github https://github.com/LauraPS1/TFEA.ChIP_downloads 上使用。该软件包还有一个基于网络的 GUI 可在 https://www.iib.uam.es/TFEA.ChIP/ 使用。
补充数据可在 Bioinformatics 在线获取。