knitr::opts_chunk$set(echo = FALSE, results = 'asis', fig.pos = 'H') knitr::knit_hooks$set(hook_convert_odg = rmdhelp::hook_convert_odg)
n_pop_size <- 200 n_line <- 4 n_year_emigration <- 1810 n_year_semen_import <- 1960 n_sex_ratio <- 0.5 n_generation_interval <- 10
Because of very low amounts of harvested corn and grains at the end of the $18^{th}$ century in central Europe, many farmers were forced to leave their contry and find a new home in the USA. In r n_year_emigration
a group of farmers took a population of about r n_pop_size
animals and moved to the US. After the arrival, the group formed r n_line
subgroups and settled in the states of Wisconsin, Virginia, Texas and Calefornia. The animals were equally partitioned to the subgroups. After the partion into the subpopulations, the animals were bred independently in the four different lines. In r n_year_semen_import
, semen from bulls of the partitioned subpopulations was re-imported to Europe.
r n_sex_ratio
$.r n_generation_interval
years.n_hom_value <- 25 n_maf_locus_a <- .1 n_diff_het <- 10 n_maf <- .05
Use the same assumptions as in Problem 1 and compute the inbreeding depression caused by the inbreeding coefficient computed in Problem 1 at two different genetic loci.
a. Locus $A$ is purely additive with a genotypic value of $a=r n_hom_value
$. Hence the genotypic value of the heterozygous genotype is in the middle between the values of the two homozygous genotypes. In other words, the quantity $d = 0$. The minor allele frequency (MAF) of the positive allele of locus $A$ is $p = r n_maf_locus_a
$
b. Locus $B$ where the valud of the heterozygous genotypes $B_1B_2$ is $10$ units above the mean of the homozygous genotypes, hence you can set the quantity $d=10$. The minor allele frequency of the positive allele of locus $B$ is $p = r n_maf
$.
Compute the between-line, the within-line and the total genetic variance for the population described in Problem 1 and the locus $A$ of Problem 2a.
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