Fig. 4: High-risk individuals identified by the platforms, at rsq ≥ 0.
From: Genomic platform specific polygenic risk scores impact breast cancer risk stratification
A PRS313 post-mean correction, allowing the number of variants used to differ with array/ lc-WGS, using the maximum number of variants with rsq ≥ 0, and B including only variants found across all platforms. Left: A matrix layout for intersections that has at least one individual. Set size denotes the number of high-risk individuals identified on each array. Dark circles indicate sets that are part of the intersection. Right: The same information on the overlaps of high-risk individuals identified depicted in a Venn diagram.
