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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)