4.7 Article

Towards a better understanding of TF-DNA binding prediction from genomic features

期刊

COMPUTERS IN BIOLOGY AND MEDICINE
卷 149, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.compbiomed.2022.105993

关键词

TF-DNA binding; Genomic features; Deep learning; Motif discovery; Noncoding variant

资金

  1. National Natural Science Foundation of China [61702058]
  2. Scientific Research Foundation of Sichuan Province [2022001]

向作者/读者索取更多资源

This paper provides a comprehensive compendium to better understand TF-DNA binding from genomic features. It summarizes commonly used datasets and data processing methods, and classifies and analyzes current deep learning methods in TFBS prediction. It also illustrates the characterization of functional consequences of TF-DNA binding and discusses the challenges and opportunities of deep learning in TF-DNA binding prediction.
Transcription factors (TFs) can regulate gene expression by recognizing specific cis-regulatory elements in DNA sequences. TF-DNA binding prediction has become a fundamental step in comprehending the underlying cis-regulation mechanism. Since a particular genome region is bound depending on multiple features, such as the arrangement of nucleotides, DNA shape, and an epigenetic mechanism, many researchers attempt to develop computational methods to predict TF binding sites (TFBSs) based on various genomic features. This paper provides a comprehensive compendium to better understand TF-DNA binding from genomic features. We first summarize the commonly used datasets and data processing manners. Subsequently, we classify current deep learning methods in TFBS prediction according to their utilized genomic features and analyze each technique's merit and weakness. Furthermore, we illustrate the functional consequences characterization of TF-DNA binding by prioritizing noncoding variants in identified motif instances. Finally, the challenges and opportunities of deep learning in TF-DNA binding prediction are discussed. This survey can bring valuable insights for researchers to study the modeling of TF-DNA binding.

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