Global changes in open chromatin (cut sites) could be characterized by two main observations: (1) a decreasing trend in the chromatin accessibility of immune cells from FT to naive tumors and then to NACT tumors and (2) a general increasing trend in open chromatin sites in endothelial cells, fibroblasts, and epithelial cells from naive tumors to NACT tumors ( Figure S2C ).
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Single-cell resolution of an open chromatin signature in persister tumor cells.
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