Abstract

Topologically associated domains (TADs) represent essential units constituting chromatin’s intricate three-dimensional spatial organization. TADs are stably present across cell types and species, and their influence on vital biological processes, such as gene expression, DNA replication, and chromosomal translocation, underscores their significance. Accordingly, the identification of TADs within the Hi-C interaction matrix is a key point in three-dimensional genomics. TADs manifest as contiguous blocks along the diagonal of the Hi-C interaction matrix, which are characterized by dense interactions within blocks and sparse interactions between blocks. An optimization method is proposed to enhance Hi-C interaction matrix data using the empirical mode decomposition method, which requires no prior knowledge and adaptively decomposes Hi-C data into a sum of multiple eigenmodal functions via exploiting the inherent characteristics of variations in the input Hi-C data. We identify TADs within the optimized data and compared the results with five commonly used TAD detection methods, namely the Directionality Index (DI), Interaction Isolation (IS), HiCKey, HiCDB, and TopDom. The results demonstrate the universality and efficiency of the proposed method, highlighting its potential as a valuable tool in TAD identification.

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