| Literature DB >> 34607350 |
Shuangquan Zhang1, Anjun Ma2, Jing Zhao2, Dong Xu3, Qin Ma2, Yan Wang1,4.
Abstract
Identifying cis-regulatory motifs from genomic sequencing data (e.g. ChIP-seq and CLIP-seq) is crucial in identifying transcription factor (TF) binding sites and inferring gene regulatory mechanisms for any organism. Since 2015, deep learning (DL) methods have been widely applied to identify TF binding sites and predict motif patterns, with the strengths of offering a scalable, flexible and unified computational approach for highly accurate predictions. As far as we know, 20 DL methods have been developed. However, without a clear and systematic assessment, users will struggle to choose the most appropriate tool for their specific studies. In this manuscript, we evaluated 20 DL methods for cis-regulatory motif prediction using 690 ENCODE ChIP-seq, 126 cancer ChIP-seq and 55 RNA CLIP-seq data. Four metrics were investigated, including the accuracy of motif finding, the performance of DNA/RNA sequence classification, algorithm scalability and tool usability. The assessment results demonstrated the high complementarity of the existing DL methods. It was determined that the most suitable model should primarily depend on the data size and type and the method's outputs.Entities:
Keywords: CLIP-seq; ChIP-seq; TF binding sites identification; deep learning method assessment; motif prediction
Mesh:
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Year: 2022 PMID: 34607350 PMCID: PMC8769700 DOI: 10.1093/bib/bbab374
Source DB: PubMed Journal: Brief Bioinform ISSN: 1467-5463 Impact factor: 13.994