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Table 4

From: Effective normalization for copy number variation detection from whole genome sequencing

FREEC Normalization UG1 UG2 YRI1 YRI2 CEU CEf Yh1 KOR
GC content 13% 12% 28% 20% 12% 24% 11% 21%
Mappability 30% 29% 79% 51% 48% 80% 36% 45%
Control genome (in Population) 10% 21% 37% 51% 14% 56% 13% 21%
Control genome (YRI1) 22% 21% - 51% 21% 38% 17% 25%
Control genome (YRI2) 26% 24% 37% - 17% 32% 22% 23%