粘蛋白
染色质
CTCF公司
计算机科学
染色体构象捕获
DNA
计算生物学
基因组
染色体
基因
生物
遗传学
基因表达
增强子
作者
Anup Kumar Halder,Abhishek Agarwal,Sevastianos Korsak,Karolina Jodkowska,Dariusz Plewczyński
标识
DOI:10.1007/978-3-031-45170-6_91
摘要
Chromosome conformation capture technologies have advanced the understanding of chromatin organization and interaction in three dimensions, giving insight into gene regulation, disease development, and cell differentiation. However, due to experimental and technical limitations, it is only possible to identify a limited number of potential genome-wide chromatin loops in all tissues or cell types of interest. Therefore we developed the "ccLoopER" method to predict genome-wide chromatin loops mediated by architectural proteins (CTCF and Cohesin) using the DNA language model and DNA-based transformer model. The ccLoopER shows significant performance improvement compared to the state-of-the-art approaches. In addition, a polymer model-specific validation shows the high similarity between real and insilico interactions (Pearson correlation: 0.955).
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