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用于推断转录因子活性的计算工具。

Computational tools for inferring transcription factor activity.

机构信息

Goethe University Frankfurt, Frankfurt am Main, Germany.

German Center for Cardiovascular Research, Partner site Rhein-Main, Frankfurt am Main, Germany.

出版信息

Proteomics. 2023 Dec;23(23-24):e2200462. doi: 10.1002/pmic.202200462. Epub 2023 Sep 14.

Abstract

Transcription factors (TFs) are essential players in orchestrating the regulatory landscape in cells. Still, their exact modes of action and dependencies on other regulatory aspects remain elusive. Since TFs act cell type-specific and each TF has its own characteristics, untangling their regulatory interactions from an experimental point of view is laborious and convoluted. Thus, there is an ongoing development of computational tools that estimate transcription factor activity (TFA) from a variety of data modalities, either based on a mapping of TFs to their putative target genes or in a genome-wide, gene-unspecific fashion. These tools can help to gain insights into TF regulation and to prioritize candidates for experimental validation. We want to give an overview of available computational tools that estimate TFA, illustrate examples of their application, debate common result validation strategies, and discuss assumptions and concomitant limitations.

摘要

转录因子 (TFs) 是调控细胞内调控景观的重要参与者。然而,它们的确切作用方式和对其他调控方面的依赖仍然难以捉摸。由于 TFs 具有细胞类型特异性,并且每个 TF 都有其自身的特点,因此从实验的角度来看,理清它们的调控相互作用是繁琐和复杂的。因此,正在开发各种计算工具,这些工具可以根据 TFs 与其假定靶基因的映射,或者以全基因组、基因非特异性的方式,从各种数据模式估计转录因子活性 (TFA)。这些工具可以帮助深入了解 TF 调控,并为实验验证确定候选者。我们希望概述可用于估计 TFA 的计算工具,举例说明它们的应用,讨论常见的结果验证策略,并讨论假设和随之而来的局限性。

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