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. 2013 Jul;194(3):769–779. doi: 10.1534/genetics.113.150169

Table 2. Power of different methods in a disease model in which only rare variants (MAF ≤ 1%) are causal with relative risk of 5 (ci = 0.2).

Error rate Coverage per person C-alpha Freq-weight VT RWAS LRT_G VST LRT
0 4 0.731 0.786 0.879 0.425 0.6 0.473 0.867
10 0.778 0.801 0.898 0.43 0.623 0.481 0.872
20 0.782 0.806 0.896 0.433 0.631 0.489 0.866
0.01 4 0.5 0.68 0.802 0.376 0.524 0.257 0.838
10 0.759 0.809 0.898 0.446 0.628 0.479 0.896
20 0.784 0.815 0.908 0.438 0.621 0.475 0.887

Tested methods were C-alpha (Neale et al. 2011), Freq-weight similar to the Madsen–Browning method (Madsen and Browning 2009), variable threshold (VT) (Price et al. 2010), RWAS (Sul et al. 2011b), LRT_G (Sul et al. 2011a), and our proposed methods (VST and LRT).