“…The five main immunohistological subtypes (by order of incidence: high-grade serous, endometrioid, clear cell, low-grade serous, and mucinous) differ vastly in terms of their stage of presentation [18], chemosensitivity [19], overall survival, and driver genetic mutations [20]. Within high-grade serous ovarian cancer, numerous studies have demonstrated heterogeneity at the level of gene sequence, gene expression, copy number, or methylation [21–27].…”