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Number of disease & injury traits: | 24 |
Number of QTL / associations found: | 1,283 |
Number of chromosomes where QTL / associations are found: | 32 |
Chromosomes | Total χ2 | df | p-values | FDR * | Size of χ2 |
Chromosome X | 542.10960 | 31 | 1.149928e-94 | 3.345245e-94 | ![]() |
Chromosome 1 | 12224.66616 | 31 | 9e-41 | 1.600000e-40 | ![]() |
Chromosome 2 | 401.73864 | 31 | 4.606112e-66 | 1.133812e-65 | ![]() |
Chromosome 3 | 16278.29064 | 31 | 9e-41 | 1.600000e-40 | ![]() |
Chromosome 4 | 37.41768 | 31 | 0.1981696 | 2.348677e-01 | ![]() |
Chromosome 5 | 49.50168 | 31 | 0.01878600 | 2.404608e-02 | ![]() |
Chromosome 6 | 118.90152 | 31 | 3.160753e-12 | 4.214337e-12 | ![]() |
Chromosome 7 | 14.40912 | 31 | 0.995149 | 9.983293e-01 | ![]() |
Chromosome 8 | 195.97104 | 31 | 7.262963e-26 | 1.056431e-25 | ![]() |
Chromosome 9 | 218.23128 | 31 | 4.982455e-30 | 7.971928e-30 | ![]() |
Chromosome 10 | 2.62416 | 31 | 0.998329325823115 | 9.983293e-01 | ![]() |
Chromosome 11 | 22.22808 | 31 | 0.8757185 | 9.983293e-01 | ![]() |
Chromosome 12 | 616.56024 | 31 | 5.02771e-110 | 2.298382e-109 | ![]() |
Chromosome 13 | 0.71616 | 31 | 0.998329325823115 | 9.983293e-01 | ![]() |
Chromosome 14 | 39.21336 | 31 | 0.1477572 | 1.818550e-01 | ![]() |
Chromosome 15 | 3822.04728 | 31 | 9e-41 | 1.600000e-40 | ![]() |
Chromosome 16 | 6094.95768 | 31 | 9e-41 | 1.600000e-40 | ![]() |
Chromosome 17 | 266.34360 | 31 | 3.111648e-39 | 5.240670e-39 | ![]() |
Chromosome 18 | 20.88144 | 31 | 0.9150033 | 9.983293e-01 | ![]() |
Chromosome 19 | 578.73648 | 31 | 3.291666e-102 | 1.170370e-101 | ![]() |
Chromosome 20 | 118.90152 | 31 | 3.160753e-12 | 4.214337e-12 | ![]() |
Chromosome 21 | 472.44792 | 31 | 2.113410e-80 | 5.635760e-80 | ![]() |
Chromosome 22 | 578.73648 | 31 | 3.291666e-102 | 1.170370e-101 | ![]() |
Chromosome 23 | 347.49096 | 31 | 3.426168e-55 | 7.831241e-55 | ![]() |
Chromosome 24 | 655.58136 | 31 | 4.104092e-118 | 4.377698e-117 | ![]() |
Chromosome 25 | 655.58136 | 31 | 4.104092e-118 | 4.377698e-117 | ![]() |
Chromosome 26 | 195.97104 | 31 | 7.262963e-26 | 1.056431e-25 | ![]() |
Chromosome 27 | 542.10960 | 31 | 1.149928e-94 | 3.345245e-94 | ![]() |
Chromosome 28 | 655.58136 | 31 | 4.104092e-118 | 4.377698e-117 | ![]() |
Chromosome 29 | 616.56024 | 31 | 5.02771e-110 | 2.298382e-109 | ![]() |
Chromosome 30 | 616.56024 | 31 | 5.02771e-110 | 2.298382e-109 | ![]() |
Chromosome 31 | 616.56024 | 31 | 5.02771e-110 | 2.298382e-109 | ![]() |
Traits | Total χ2 | df | p-values | FDR * | Size of χ2 |
Bone fracture | 354.47196 | 23 | 3.872768e-61 | 1.549107e-60 | |
Degenerative suspensory ligament desmitis | 96.12375 | 23 | 6.522354e-11 | 8.696472e-11 | |
Dwarfism | 40.94975 | 23 | 0.01199995 | 1.252169e-02 | |
Equine arteritis virus | 697.97056 | 23 | 1.187942e-132 | 2.851061e-131 | |
Equine herpesvirus type 1-induced myeloencephalopathy | 48.34616 | 23 | 0.001510571 | 1.647896e-03 | |
Equine metabolic syndrome | 75.62275 | 23 | 1.599446e-07 | 1.919335e-07 | |
Equine neuroaxonal dystrophy/degenerative myeloencephalopathy | 352.76631 | 23 | 8.640403e-61 | 2.962424e-60 | |
Equine sarcoids | 101.27313 | 23 | 8.480679e-12 | 1.197272e-11 | |
Foal Immunodeficiency Syndrome | 171.95456 | 23 | 8.950255e-25 | 1.652355e-24 | |
Guttural pouch tympany | 683.70867 | 23 | 1.196359e-129 | 1.435631e-128 | |
Hydrocephalus | 556.40061 | 23 | 6.109662e-103 | 4.887730e-102 | |
Insect bite hypersensitivity | 169.27079 | 23 | 2.909425e-24 | 4.987586e-24 | |
Laminitis | 39.09376 | 23 | 0.01937564 | 1.937564e-02 | |
Melanoma | 546.85715 | 23 | 6.022189e-101 | 3.613313e-100 | |
Osteochondrosis | 139.21363 | 23 | 1.294856e-18 | 2.071770e-18 | |
Osteochondrosis dissecans | 274.16948 | 23 | 7.278496e-45 | 2.183549e-44 | |
Overriding spinous processes | 364.57142 | 23 | 3.328983e-63 | 1.597912e-62 | |
Recurrent airway obstruction | 177.11233 | 23 | 9.223638e-26 | 1.844728e-25 | |
Recurrent exertional rhabdomyolysis | 206.75909 | 23 | 1.678302e-31 | 4.027925e-31 | |
Recurrent laryngeal neuropathy | 76.66235 | 23 | 1.092497e-07 | 1.379996e-07 | |
Recurrent uveitis | 120.52755 | 23 | 3.343712e-15 | 5.015568e-15 | |
Rhodococcus equi infection | 181.55915 | 23 | 1.291149e-26 | 2.817052e-26 | |
Vitiligo | 54.06708 | 23 | 0.0002621166 | 2.995618e-04 | |
chronic progressive lymphedema | 214.99507 | 23 | 4.09955e-33 | 1.093213e-32 |
No correlation data found on these traits |
Data | ![]() |
Chi'Square Test | ![]() |
Fisher's Exact Test | |||
Number of chrom.: | 32 | χ2 | = | 47617.628160 | |||
Number of traits: | 24 | df | = | 713 | |||
Number of QTLs: | 1,283 | p-value | = | 0 |
FOOT NOTE: * : FDR is short for "false discovery rate", representing the expected proportion of type I errors. A type I error is where you incorrectly reject the null hypothesis, i.e. you get a false positive. It's statistical definition is FDR = E(V/R | R > 0) P(R > 0), where V = Number of Type I errors (false positives); R = Number of rejected hypotheses. Benjamini–Hochberg procedure is a practical way to estimate FDR.
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USA · USDA · NRPSP8 · Program to Accelerate Animal Genomics Applications.
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