Objective: A genomic region associated with a particular phenotype is called QTL. To detect the optimal F 2 population size associated with QTLs in native chicken, we performed a simulation study on F 2 population derived from crosses between two different breeds.Methods: A total of 15 males and 150 females were randomly selected from the last generation of each F 1 population which was composed of different breed to create two different F 2 populations.The progenies produced from these selected individuals were simulated for six more generations.Their marker genotypes were simulated with a density of 50K at three different heritability levels for the traits such as 0.1, 0.3 and 0.5. Our study is that to compare 100, 500, 1000 TPreference population (RP) groups to each other with three different heritability levels. And a total of 35 QTLs were used, and their locations were randomly created.Results: With a TPRP size of 100, no QTL was detected to satisfy Bonferroni value at three different heritability levels. In a TPRP size of 500, two QTLs were detected when the heritability was 0.5. With a TPRP size of 1,000, 0.1 heritability was detected only one QTL, and 0.5 heritability shows that five QTLs were detected. To sum up, TPRP size and heritability are playing a key role to detect QTLs in QTL study. The larger TPRP size and greater heritability value, the higher the probability of detection of QTLs.With a TPRP size of 100, some QTLs were found, even though the number of QTLs were somewhat similar for h 2 = 0.1, 0.3, and 0.5, respectively. This result indicates an increased in h 2 did not improve number of QTLs at TPRP size of 100. With a TPRP size of 1000, many QTLs were detected at different h 2 levels of traits, even at the h 2 value of 0.1
Conclusion:Our study suggests that the use of a large TPRP and heritability can improve QTL detection in an F 2 chicken population.