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基于全基因组 ChIP-X 数据的基因调控网络计算推断。

Computational Inference of Gene Regulatory Network Using Genome-wide ChIP-X Data.

机构信息

Department of Systems and Computational Biology, School of Life Sciences, University of Hyderabad, Hyderabad, Telangana, India.

出版信息

Methods Mol Biol. 2024;2719:295-306. doi: 10.1007/978-1-0716-3461-5_16.

Abstract

Gene regulatory network is the architecture of transcription factors (TFs) and their gene targets, which help in controlling their expression as required by a phenotype during various environmental perturbations. Inferring the regulatory network from the high-throughput data needs an algorithmic approach involving statistical analysis. There are several interaction databases such as JASPAR and SwissRegulon that provide information for TFs-targets pair interaction, which are estimated based on experimental and prediction procedures. These repositories are majorly used for predicting the complex structure of GRNs either with or without gene expression data. Here we described and discussed the step-wise procedures to extract the interaction data for a desired set of target-TFs from the JASPAR database, and used that information to infer the network by using the igraph library. Further, we also mentioned the important parameters for analyzing the different properties of the network. The described procedure will be helpful in discerning the GRN based on the set of TF-gene pairs.

摘要

基因调控网络是转录因子(TFs)及其基因靶标的结构,有助于在各种环境扰动下控制表型所需的表达。从高通量数据中推断调控网络需要一种涉及统计分析的算法方法。有几个交互数据库,如 JASPAR 和 SwissRegulon,提供了 TF-靶标对相互作用的信息,这些信息是基于实验和预测程序估计的。这些存储库主要用于预测 GRN 的复杂结构,无论是有还是没有基因表达数据。在这里,我们描述和讨论了从 JASPAR 数据库中提取目标-TF 所需的交互数据的逐步过程,并使用igraph 库使用该信息推断网络。此外,我们还提到了分析网络不同性质的重要参数。所描述的过程将有助于根据 TF-基因对集来识别 GRN。

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