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These were then crossed to ♂-SRC(1) and ♂-ParisC(1) sires.
As shown in Table 1, sires carrying susceptible variations of FEZL and IGF1R are common in Japan.
For comparison, ♂-SRC(1) and ♂-ParisC(1) sires (which have identical maternal effects and genetic backgrounds except for the X chromosomes) also were mated to EVEN females (100 matings of 1♂ × 2♀ for each type of sire), and the sex ratio of their families was measured.
Similar(57)
Simulated populations resulted from a nested mating design (1 sire to 2 dams).
The mapping population consisted of 10 sires and their 417 sons in a granddaughter design.
Each sire was mated to two dams, and each dam was mated to two sires, producing 50 viable full-sib families (29 sires, 25 dams).
Partial factorial and nested mating designs were used, respectively, to generate the G2 and G3 generations, with 162 and 156 full-sib families (from 95 sires and 97 dams, and 93 sires and 156 dams in the two generations, respectively).
In this experiment, we evaluated 600 young sea bass from a factorial mating of 76 sires and 13 dams.
In strategy RAND, 10 sires and 10 dams were randomly selected from the 82 parents to form the base population.
In strategy HET, we chose the 10 sires and 10 dams with the highest average heterozygosity across all markers.
Each year 10 sires and 100 dams were selected to produce the next generation of male and female selection candidates.
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