From: An efficient unified model for genome-wide association studies and genomic selection
\(h^{2}\) | nQTLa | Number of detected causal SNPs | Mapping precision | ||||||
---|---|---|---|---|---|---|---|---|---|
0Â kb | 10Â kb | 20Â kb | 30Â kb | 0Â kb | 10Â kb | 20Â kb | 30Â kb | ||
0.25 | 7.78 (0.345) | 5.01 (0.171) | 6.22 (0.154) | 6.54 (0.154) | 6.69 (0.132) | 0.65 (0.022) | 0.80 (0.019) | 0.84 (0.019) | 0.86 (0.017) |
0.50 | 18.52 (0.522) | 12.22 (0.333) | 15.37 (0.222) | 15.37 (0.185) | 16.67 (0.167) | 0.66 (0.018) | 0.83 (0.012) | 0.87 (0.010) | 0.90 (0.009) |
0.75 | 34.22 (0.640) | 23.95 (0.376) | 29.42 (0.308) | 30.80 (0.240) | 31.82 (0.205) | 0.70 (0.011) | 0.86 (0.009) | 0.90 (0.007) | 0.93 (0.006) |