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Significance Chromatin plays a critical role in the regulation of gene expression. Interactions among chromatin regulators, sequence-specific transcription factors, and cis -regulatory sequence elements are the main driving forces shaping context-specific chromatin structure and gene expression. However, because of the large number of such interactions, direct data on them are often missing in most cellular contexts. The purpose of the present work is to show that, by modeling matched expression and accessibility data across diverse cellular contexts, it is possible to recover a significant portion of the information in the missing data on binding locations and chromatin states and to achieve accurate inference of gene regulatory relations.
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Duren et al. (2017) studied this question.
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