Wenying He , Haolu Zhou , Yun Zuo , Yude Bai , Fei Guo
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These types of feature vectors are conducted and combined by neural networks, which aim at SE prediction. To validate the effectiveness of MuSE, we design extensive experiments on human and mouse species datasets. Compared to baselines such as SENet, MuSE improves the prediction of F1 score to a maximum improvement exceeding 0.05 on mouse species. The k-mer representations based on DNA2Vec among the given features have the most important impact on predictions. This feature effectively captures context semantic knowledge and positional information of DNA sequences. However, its representation of the individuality of each species negatively affects MuSE's generalization ability. Nevertheless, the cross-species prediction results of MuSE improve again to reach an AUC of nearly 0.8, after removing this type of feature. 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This feature effectively captures context semantic knowledge and positional information of DNA sequences. However, its representation of the individuality of each species negatively affects MuSE's generalization ability. Nevertheless, the cross-species prediction results of MuSE improve again to reach an AUC of nearly 0.8, after removing this type of feature. 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引用次数: 0
摘要
虽然基于生物信息学的方法能准确识别 SE(超级增强子),但其结果取决于特征设计。如何表示生物序列并自动提取其关键特征以提高 SE 识别率是基础。我们提出了一种基于多特征融合的深度学习模型 MuSE(Multi-Feature Fusion for Super-Enhancer)。该模型利用两种编码方法(one-hot 和 DNA2Vec)来标识 DNA 序列。具体来说,one-hot 编码反映的是单核苷酸信息,而基于 DNA2Vec 的 k-mer 表示法捕捉的是局部序列片段信息和全局序列特征。神经网络对这些类型的特征向量进行处理和组合,从而实现 SE 预测。为了验证 MuSE 的有效性,我们在人类和小鼠物种数据集上进行了大量实验。与 SENet 等基线相比,MuSE 提高了小鼠物种的 F1 分数预测,最大提高幅度超过了 0.05。在给定的特征中,基于 DNA2Vec 的 k-mer 表示对预测的影响最大。该特征能有效捕捉 DNA 序列的上下文语义知识和位置信息。但是,它对每个物种个体性的表征对 MuSE 的泛化能力产生了负面影响。尽管如此,在去除这类特征后,MuSE 的跨物种预测结果再次得到改善,AUC 接近 0.8。源代码见 https://github.com/15831959673/MuSE。
MuSE: A deep learning model based on multi-feature fusion for super-enhancer prediction
Although bioinformatics-based methods accurately identify SEs (Super-enhancers), the results depend on feature design. It is foundational to representing biological sequences and automatically extracting their key features for improving SE identification. We propose a deep learning model MuSE (Multi-Feature Fusion for Super-Enhancer), based on multi-feature fusion. This model utilizes two encoding methods, one-hot and DNA2Vec, to signify DNA sequences. Specifically, one-hot encoding reflects single nucleotide information, while k-mer representations based on DNA2Vec capture both local sequence fragment information and global sequence characteristics. These types of feature vectors are conducted and combined by neural networks, which aim at SE prediction. To validate the effectiveness of MuSE, we design extensive experiments on human and mouse species datasets. Compared to baselines such as SENet, MuSE improves the prediction of F1 score to a maximum improvement exceeding 0.05 on mouse species. The k-mer representations based on DNA2Vec among the given features have the most important impact on predictions. This feature effectively captures context semantic knowledge and positional information of DNA sequences. However, its representation of the individuality of each species negatively affects MuSE's generalization ability. Nevertheless, the cross-species prediction results of MuSE improve again to reach an AUC of nearly 0.8, after removing this type of feature. Source codes are available at https://github.com/15831959673/MuSE.
期刊介绍:
Computational Biology and Chemistry publishes original research papers and review articles in all areas of computational life sciences. High quality research contributions with a major computational component in the areas of nucleic acid and protein sequence research, molecular evolution, molecular genetics (functional genomics and proteomics), theory and practice of either biology-specific or chemical-biology-specific modeling, and structural biology of nucleic acids and proteins are particularly welcome. Exceptionally high quality research work in bioinformatics, systems biology, ecology, computational pharmacology, metabolism, biomedical engineering, epidemiology, and statistical genetics will also be considered.
Given their inherent uncertainty, protein modeling and molecular docking studies should be thoroughly validated. In the absence of experimental results for validation, the use of molecular dynamics simulations along with detailed free energy calculations, for example, should be used as complementary techniques to support the major conclusions. Submissions of premature modeling exercises without additional biological insights will not be considered.
Review articles will generally be commissioned by the editors and should not be submitted to the journal without explicit invitation. However prospective authors are welcome to send a brief (one to three pages) synopsis, which will be evaluated by the editors.