Analyzing Genomic Features with Predictive Chromatin Interaction Models: A Comprehensive Evaluation

Yi Kou, Daniel Zhao
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Abstract

Enhancer-Promoter (EP) interactions reflected by Hi-C technology are crucial to understanding genomic functions. Particularly, identifying ‘unique’ genomic features that are characteristically important in a specific cell line can further our current understanding of the mechanisms that drive cell differentiation, tissue development, and disease progression. However, classic prediction models such as TargetFinder provide little valuable insight towards the large disparity between important genomic features across different cell lines. To comprehensively approach this question, herein we first evaluated seven classifiers to predict EP interactions using high-resolution Hi-C maps of genome loci across six classic cell lines, surpassing TargetFinder in all benchmark metrics. We then evaluated the model's predictive performance with features provided by seven feature selection methods from the embedded, wrapper and filter categories. Moreover, groups of features were aggregated from the results of two or more feature methods and analyzed based on the model's performance. Finally, we examined the distinguishing features across six cell lines. Our study suggests the existence of ‘unique’ genomic features that are especially predictive of EP interactions only in specific cell lines.
用预测染色质相互作用模型分析基因组特征:一个综合评价
Hi-C技术反映的增强子-启动子(EP)相互作用对了解基因组功能至关重要。特别是,确定在特定细胞系中具有重要特征的“独特”基因组特征可以进一步了解驱动细胞分化、组织发育和疾病进展的机制。然而,经典的预测模型,如TargetFinder,对不同细胞系之间重要的基因组特征之间的巨大差异提供了很少有价值的见解。为了全面解决这个问题,我们首先评估了7个分类器,利用6个经典细胞系基因组位点的高分辨率Hi-C图谱来预测EP相互作用,在所有基准指标上都超过了TargetFinder。然后,我们使用嵌入、包装和过滤器类别中的七种特征选择方法提供的特征来评估模型的预测性能。此外,从两种或多种特征方法的结果中聚合特征组,并根据模型的性能进行分析。最后,我们研究了六种细胞系的显著特征。我们的研究表明,存在“独特”的基因组特征,这些特征特别预测了仅在特定细胞系中的EP相互作用。
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