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Function to extract QTL effect variance for single SNP QTLs in a given gen/database/cohort
get.qtl.variance(population, gen = NULL, database = NULL, cohorts = NULL)
Population list
Quick-insert for database (vector of all generations to consider)
Groups of individuals to consider
Quick-insert for database (vector of names of cohorts to consider)
matrix with SNP / Chr / estimated effect variance
# NOT RUN { data(ex_pop) effects <- get.qtl.variance(ex_pop) # }
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