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Table 6 Gene occurrences on the plus (#P) and minus (#M) strands of HG38 display abundance of the former

From: Inversion symmetry of DNA k-mer counts: validity and deviations

chr

P

M

Y(P,M)

Z(P,M)

p values

Z(T,A)

Z(G,C)

corr

1

4488

4291

0.022

2.103

0.018

15.00

5.76

v

2

4106

3367

0.099

8.549

0

16.41

13.49

v

3

2938

2516

0.077

5.714

5.65E-09

13.19

12.50

v

4

2542

1792

0.173

11.392

0

5.75

11.04

v

5

2777

2186

0.119

8.389

0

24.44

17.50

v

6

4840

3563

0.152

13.931

0

2.72

8.12

v

7

3024

2402

0.115

8.444

0

16.15

7.57

v

8

2135

2032

0.025

1.596

0.055

−3.53

9.65

 

9

3032

2180

0.163

11.802

0

5.61

9.99

v

10

2532

2156

0.080

5.492

2.01E-08

17.18

10.82

v

11

2879

4047

−0.169

−14.035

0

8.48

10.51

x

12

3003

2771

0.040

3.053

0.0011

13.75

12.20

x

13

1261

1227

0.014

0.682

0.25

14.83

15.36

 

14

2092

1906

0.047

2.942

0.0016

32.58

22.24

v

15

4226

3547

0.087

7.702

6.77E-15

6.44

12.23

v

16

2529

1875

0.149

9.855

0

32.17

21.07

v

17

3582

2902

0.105

8.445

0

9.77

20.81

v

18

1182

1490

−0.115

−5.958

1.26E-09

19.03

47.34

x

19

3287

3036

0.040

3.157

0.00079

25.46

20.13

v

20

1258

1193

0.027

1.313

0.09500

33.22

33.70

 

21

670

779

−0.075

−2.863

0.00212

7.33

10.15

x

22

1429

1793

−0.113

−6.413

7.28E-11

−2.52

19.94

?

X

1927

1572

0.101

6.001

9.87E-10

16.73

22.23

v

Y

491

184

0.455

11.816

0.00E + 00

17.58

0.34

 
    

P < M

p> 0.05

T < A

p> 0.05

 
  1. Three of the results are insignificant (highlighted p> 0.05, q > 0.044 using FDR corrections). Four chromosomes have opposite preferences, set in italics for P < M and T < A. For all significant results we find 16 chromosomes displaying both P > M, T > A, and G > C. Chr 22 has both P < M and T < A. Last column indicates significant correlations of T-A and G-C with gene counts (positive by v and negative by x)