TABLE 1.
Schematic comparison of the main characteristics of different mapping strategies (following Darvasi and Shifman 2005)
Linkage analysis | Admixture mapping | Joint linkage and LD mapping (and inbred-by-outbred cross) | Nested association mapping | Association mapping | |
---|---|---|---|---|---|
Allele richness | Low | Low | Intermediate | High | High |
Inference from markers in identity-by-state to quantitative trait nucleotides in IBD | Low | Low to intermediate | Intermediate | High | High |
No. of SNPs required for whole-genome scan | Low | Low | Intermediate to high | Low (only high for founders) | High |
Efficiency in using sequence information | Low | Low | Intermediate | High | Intermediate |
Mapping resolution | Poor | Intermediate | Intermediate | Good | Good |
Designed mapping population | Yes or no | Yes or No | Mostly no | Yes | No |
Sensitivity to genetic heterogeneity | Low | Moderate | High | Low | High |
Repeated phenotyping | Possible | Possible | Possible | Yes | Possible |
Statistical power | Low to intermediatea | Highb | Intermediate | High | High |
With designed mapping populations such as F2, BC, or RIL, the power of linkage analysis is generally higher in plants than in humans.
Power diminishes to zero with equal allele frequencies in the ancestral population (Darvasi and Shifman 2005).