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iProm-Sigma54:一种基于 CNN 的启动子预测工具。

iProm-Sigma54: A CNN Base Prediction Tool for Promoters.

机构信息

Department of Electronics and Information Engineering, Jeonbuk National University, Jeonju 54896, Republic of Korea.

School of Pharmacy, Jeonbuk National University, Jeonju 54896, Republic of Korea.

出版信息

Cells. 2023 Mar 7;12(6):829. doi: 10.3390/cells12060829.

DOI:10.3390/cells12060829
PMID:36980170
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10047130/
Abstract

The sigma (σ) factor of RNA holoenzymes is essential for identifying and binding to promoter regions during gene transcription in prokaryotes. σ54 promoters carried out various ancillary methods and environmentally responsive procedures; therefore, it is crucial to accurately identify σ54 promoter sequences to comprehend the underlying process of gene regulation. Herein, we come up with a convolutional neural network (CNN) based prediction tool named "iProm-Sigma54" for the prediction of σ54 promoters. The CNN consists of two one-dimensional convolutional layers, which are followed by max pooling layers and dropout layers. A one-hot encoding scheme was used to extract the input matrix. To determine the prediction performance of iProm-Sigma54, we employed four assessment metrics and five-fold cross-validation; performance was measured using a benchmark and test dataset. According to the findings of this comparison, iProm-Sigma54 outperformed existing methodologies for identifying σ54 promoters. Additionally, a publicly accessible web server was constructed.

摘要

RNA 全酶的 σ 因子对于原核生物基因转录过程中识别和结合启动子区域至关重要。σ54 启动子执行各种辅助方法和环境响应程序;因此,准确识别 σ54 启动子序列对于理解基因调控的基本过程至关重要。在这里,我们提出了一种基于卷积神经网络(CNN)的预测工具,名为“iProm-Sigma54”,用于预测 σ54 启动子。CNN 由两个一维卷积层组成,后面是最大池化层和 dropout 层。采用独热编码方案提取输入矩阵。为了确定 iProm-Sigma54 的预测性能,我们采用了四种评估指标和五折交叉验证;使用基准数据集和测试数据集进行性能衡量。根据这一比较的结果,iProm-Sigma54 在识别 σ54 启动子方面优于现有的方法。此外,还构建了一个公共访问的网络服务器。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573f/10047130/269c41efae6f/cells-12-00829-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573f/10047130/a28400074133/cells-12-00829-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573f/10047130/ea6873f68c28/cells-12-00829-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573f/10047130/117eb15f9819/cells-12-00829-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573f/10047130/24a347929244/cells-12-00829-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573f/10047130/03bcbe31d93b/cells-12-00829-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573f/10047130/269c41efae6f/cells-12-00829-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573f/10047130/a28400074133/cells-12-00829-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573f/10047130/ea6873f68c28/cells-12-00829-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573f/10047130/117eb15f9819/cells-12-00829-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573f/10047130/24a347929244/cells-12-00829-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573f/10047130/03bcbe31d93b/cells-12-00829-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573f/10047130/269c41efae6f/cells-12-00829-g006.jpg

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引用本文的文献

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Front Microbiol. 2022 Nov 4;13:1061122. doi: 10.3389/fmicb.2022.1061122. eCollection 2022.
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Deep Learning Approaches for Detection of Breast Adenocarcinoma Causing Carcinogenic Mutations.深度学习方法在乳腺癌致癌突变检测中的应用
Int J Mol Sci. 2022 Sep 29;23(19):11539. doi: 10.3390/ijms231911539.
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iEnhancer-DLRA: identification of enhancers and their strengths by a self-attention fusion strategy for local and global features.
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Brief Bioinform. 2024 Mar 27;25(3). doi: 10.1093/bib/bbae193.
iEnhancer-DLRA:通过自注意力融合策略识别增强子及其强度,用于局部和全局特征。
Brief Funct Genomics. 2022 Sep 16;21(5):399-407. doi: 10.1093/bfgp/elac023.
4
PromoterLCNN: A Light CNN-Based Promoter Prediction and Classification Model.启动子 LCNN:一种基于轻量级卷积神经网络的启动子预测和分类模型。
Genes (Basel). 2022 Jun 23;13(7):1126. doi: 10.3390/genes13071126.
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Machine learning techniques for identification of carcinogenic mutations, which cause breast adenocarcinoma.机器学习技术用于鉴定致癌突变,这些突变导致乳腺腺癌。
Sci Rep. 2022 Jul 11;12(1):11738. doi: 10.1038/s41598-022-15533-8.
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Genomics. 2022 May;114(3):110384. doi: 10.1016/j.ygeno.2022.110384. Epub 2022 May 6.
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