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. 2009 Aug;182(4):1263–1277. doi: 10.1534/genetics.109.100727

TABLE 2.

Performance of single-locus and multilocus methods in mapping two QTL in 100 simulated eight-founder heterogeneous stock populations

Single locus or multilocus Threshold
False discovery rate (%)e Chromosome 2 associations (%)f
Methoda Typeb Units Valuec Power (%)d
Naive single locus Single Permutation Log P 3.65 (3.43, 3.99) 99.5 (±0.5) 92.3 (±0.28) 52.4 (±0.18)
Naive single locus Single Parametric bootstrap Log P 9.48 (5, 15.5) 90 (±2.2) 73.5 (±2.3) 9.87 (±0.11)
Mixed model Single Parametric bootstrap Log P 3.91 (3.59, 4.33) 89.5 (±2.3) 69.5 (±2.1) 2.41 (±0.056)
Single locus Single ∼80% power Log P 9.88 80 (±3.4) 63.3 (±3.5) 7.39 (±0.095)
Mixed model Single ∼80% power Log P 5.13 80 (±2.9) 46.6 (±3) 0.702 (±0.03)
Bagging Multilocus ∼80% power Range probability 0.39 80 (±2.8) 22.4 (±2.6) 0 (±0)
Bagging peaks 1 cM Multilocus ∼80% power Range probability 0.39 80 (±2.8) 12.8 (±2.5) 0.0584 (±0.041)
Bagging peaks 2 cM Multilocus ∼80% power Range probability 0.34 80 (±2.9) 23.5 (±2.8) 0.54 (±0.16)
Bagging peaks 4 cM Multilocus ∼80% power Range probability 0.29 80.5 (±2.8) 30.4 (±2.7) 1.92 (±0.37)
Bagging peaks 8 cM Multilocus ∼80% power Range probability 0.23 80.5 (±2.7) 43.1 (±2.5) 7.95 (±0.95)
Subagging Multilocus ∼80% power Range probability 0.4 80 (±3) 16 (±2.8) 0.00264 (±0.0019)
Subagging peaks 1 cM Multilocus ∼80% power Range probability 0.34 80 (±2.8) 19.8 (±2.8) 0.204 (±0.077)
Subagging peaks 2 cM Multilocus ∼80% power Range probability 0.27 80 (±2.8) 23.3 (±2.9) 0.585 (±0.16)
Subagging peaks 4 cM Multilocus ∼80% power Range probability 0.22 80.5 (±2.9) 28.7 (±3) 2.42 (±0.41)
Subagging peaks 8 cM Multilocus ∼80% power Range probability 0.14 80 (±2.8) 35.9 (±2.9) 7.33 (±0.91)
a

All subagging uses 80% subsamples. The suffix “peaks p cM” denotes where model selection chose among representative peaks from a naive single locus scan rather than among all loci (see simulations).

b

How the threshold for calculating performance statistics was determined and applied. Permutation: genomewide 5% significance thresholds were calculated separately for each simulation. Parametric bootstrap: thresholds were calculated separately for each simulation. “∼n% power”: scores were pooled for all simulations and the threshold was calibrated to give ∼n% power.

c

For the permutation and parametric bootstrap results, threshold values are given as “median (lowest, highest).” Otherwise the numbers are the range probability thresholds required to achieve ∼n% power.

d

The proportion of segments containing QTL that had scores above the threshold, averaged over simulations (SE in parentheses).

e

The proportion of 6-cM segments with scores above the threshold that did not contain a QTL, averaged over simulations (SE in parentheses).

f

The proportion of marker intervals on chromosome 2 predicted to contain QTL, averaged over simulations (SE in parentheses).