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Table 2 shows the basic coverage statistics for the OXTR sequence and for the guide RNA-dependent fragments

From: A targeted long-read sequencing approach questions the association of OXTR methylation with high-functioning autism

 

Coverage

t test (coverage~group)

 

Genomic ranges (chr3:)

M

SD

Min

Max

t

df

p

OXTR overall

8,750,381–8,770,434

29.233

24.124

6.790

142.394

− 0.515

26.489

0.611

HFA

 

31.216

31.371

9.240

142.394

   

NC

 

27.250

14.217

6.790

47.521

   

Fragment 1

8.761.480–8.749.344

20.167

20.092

3.507

125.959

− 0.826

24.427

0.417

HFA

 

22.802

26.654

3.507

125.959

   

NC

 

17.533

10.179

3.610

36.240

   

Fragment 2

8.770.937–8.763.067

34.221

26.820

6.908

151.238

− 0.378

27.654

0.709

HFA

 

35.841

34.429

9.820

151.238

   

NC

 

32.601

16.900

6.908

60.927

   
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Clinical Epigenetics

ISSN: 1868-7083

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