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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%