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. 2020 Aug 17;117(35):21364–21372. doi: 10.1073/pnas.1922703117

Fig. 1.

Fig. 1.

Model design. (A) Schematic overview of the OpenCausal approach. OpenCausal captures the change of chromatin accessibility caused by a variant, where the variation is derived from WGS data. (B) Schematic overview of the Ropen model. Ropen is a sequence-based regression model that predicts chromatin accessibility score for a RE using the expression of TFs binding on this region.