Table 4. Results of single-marker (GenABEL) and Bayesian (GenSel) genome-wide association analysis for susceptibility to MAP infection in Jersey cattle (combined data, N = 1,069)1.
SNP | BTA5 | Position6 | A17 | A28 | Effect B (SE)9 | P-value10 | Q.2 (Cases)11 | Q.2 (Controls)12 | GenSel Rank13 | Window (SNPs)14 | %GV15 | P> avg.16 | Model freq.17 |
Common SNPs 2 | |||||||||||||
ARS-BFGL-NGS-11887 | 23 | 27 776 075 | A | G | –0.077 (0.02) | 8.5×10−5 | 0.35 | 0.44 | 1 | 2199 (18) | 3.21 | 0.29 | 0.23 |
Hapmap45793-BTA-114539 | 11 | 93 027 457 | A | T | 0.081 (0.022) | 1.3×10−4 | 0.32 | 0.25 | 6 | 1318 (8) | 1.47 | 0.15 | 0.16 |
ARS-BFGL-NGS-92339 | 23 | 19 397 902 | C | A | –0.10 (0.027) | 1.5×10−4 | 0.12 | 0.18 | 10 | 2191 (18) | 0.99 | 0.12 | 0.09 |
ARS-BFGL-NGS-109837 | 3 | 100 901 542 | A | C | –0.072 (0.020) | 1.6×10−4 | 0.43 | 0.51 | 2 | 399 (18) | 2.12 | 0.19 | 0.15 |
BTA-56690-no-rs | 23 | 44 458 259 | A | G | –0.109 (0.030) | 1.8×10−4 | 0.10 | 0.15 | 19 | 2216 (18) | 0.59 | 0.08 | 0.04 |
Hapmap53765-ss46526662 | 3 | 107 097 209 | G | A | –0.07 (0.020) | 2.9×10−4 | 0.33 | 0.41 | 5 | 406 (13) | 1.52 | 0.12 | 0.08 |
ARS-BFGL-NGS-20015 | 11 | 92 692 190 | G | A | 0.071 (0.020) | 3×10−4 | 0.43 | 0.35 | 4 | 1317 (15) | 1.56 | 0.16 | 0.08 |
BTB-00148619 | 3 | 106 442 016 | A | G | –0.069 (0.020) | 3.1×10−4 | 0.36 | 0.45 | 9 | 405 (15) | 1.02 | 0.11 | 0.09 |
ARS-BFGL-NGS-100555 | 17 | 57 131 089 | A | G | 0.07 (0.020) | 3.9×10−4 | 0.42 | 0.33 | 7 | 1818 (16) | 1.28 | 0.13 | 0.1 |
ARS-BFGL-BAC-35219 | 23 | 29 316 835 | G | A | –0.085 (0.025) | 4.0×10−4 | 0.17 | 0.23 | 20 | 2201 (9) | 0.57 | 0.07 | 0.04 |
BTA-75232-no-rs | 5 | 10 104 621 | G | A | –0.066 (0.010) | 4.8×10−4 | 0.45 | 0.54 | 11 | 554 (14) | 0.93 | 0.1 | 0.1 |
ARS-BFGL-NGS-26988 | 3 | 6 183 874 | G | A | –0.081 (0.024) | 4.8×10−4 | 0.18 | 0.24 | 18 | 305 (11) | 0.62 | 0.07 | 0.06 |
ARS-BFGL-NGS-95270 | 25 | 19 724 505 | G | A | –0.073 (0.022) | 5.1×10−4 | 0.25 | 0.52 | 3 | 2308 (13) | 1.57 | 0.16 | 0.08 |
BTA-30686-no-rs | 6 | 60 692 672 | A | C | 0.068 (0.020) | 5.4×10−4 | 0.42 | 0.34 | 12 | 727 (10) | 0.82 | 0.1 | 0.09 |
ARS-BFGL-NGS-117495 | 3 | 36 531 738 | C | A | 0.069 (0.020) | 5.2×10−4 | 0.40 | 0.32 | 14 | 335 (5) | 0.72 | 0.08 | 0.08 |
Hapmap51790-BTA-103080 | 3 | 101 076 596 | A | G | –0.067 (0.020) | 5.6×10−4 | 0.40 | 0.48 | 13 | 400 (12) | 0.79 | 0.09 | 0.05 |
SNPs (GenABEL only) 3 | |||||||||||||
ARS-BFGL-BAC-18843 | 17 | 26 318 464 | A | G | –0.194 (0.051) | 9.0×10−5 | 0.02 | 0.06 | - | - | - | - | - |
ARS-BFGL-NGS-38764 | 13 | 77 546 073 | G | A | –0.183 (0.052) | 2.7×10−4 | 0.02 | 0.05 | - | - | - | - | - |
BTB-01324240 | 13 | 1 867 669 | A | G | –0.161 (0.047) | 4.1×10−4 | 0.03 | 0.06 | - | - | - | - | - |
BTA-22128-no-rs | 6 | 13 040 713 | A | G | –0.116 (0.035) | 5.8×10−4 | 0.06 | 0.11 | - | - | - | - | - |
SNPs (GenSel only) 4 | |||||||||||||
BTB-00643802 | 16 | 48 725 717 | - | - | - | - | - | - | 8 | 1727 (17) | 1.17 | 0.11 | 0.03 |
ARS-BFGL-NGS-2973 | 3 | 102 289 610 | - | - | - | - | - | - | 15 | 401 (12) | 0.69 | 0.07 | 0.04 |
ARS-BFGL-NGS-31524 | 23 | 50 747 363 | - | - | - | - | - | - | 16 | 2222 (17) | 0.63 | 0.08 | 0.03 |
BTB-01124458 | 13 | 6 683 656 | - | - | - | - | - | - | 17 | 1430 (11) | 0.62 | 0.07 | 0.04 |
Only the twenty most significant SNPs are shown.
SNPs identified commonly by both GenABEL and GenSel analyses; order is based on P-values from GenABEL.
SNPs identified only by GenABEL.
SNPs identified only by GenSel.
Bos Taurus chromosomes.
Position of SNP based on Bovine genome build UMD 3.1 (in base pair).
Major allele.
Minor allele.
Estimated effect of allele B (fitted allele) and the standard error of the estimated effect in the parenthesis.
P-value corrected by genomic control approach (GC).
Frequency of B allele in cases.
Frequency of B allele in controls.
Rank based on percentage of genetic variance among the twenty most significant windows by GenSel analysis.
Number of 1-Mb non-overlapping genome window and number of SNPs within each window in the parenthesis.
Percentage of total genetic variance explained by 1-Mb windows.
Proportion of models in which the corresponding window accounted for > 0.04% of genetic variance (expected variance if each window had the same effect: 1/total number of windows = 2,657).
Proportion of MCMC iterations that included the corresponding SNP.