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Commit d5572d89 authored by Marie Bourdon's avatar Marie Bourdon
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modif names tab_mark

parent c62185f3
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.Rproj.user/9DAE6990/sources/s-39B546A6/8DB3123E 0 → 100644
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......
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......@@ -86,7 +86,7 @@ genos <- genos %>% filter(!Sample.ID %in% c("StrainsA_1", "StrainsA_2", "Strains
The first step of the markers sorting is to create the marker dataframe with the tab_mark() function. This dataframe contains for each marker the two alleles that can be found in the F2/N2 population (`Allele_1` and `Allele_2`), the number of individuals for each genotype (homozygous for each allele (`n_HM1` and `n_HM2`) and heterozygous (`n_HT`)), and the number of non genotyped individuals (`n_NA`) This step can take several minutes. You can also load the output of this function.
```{r tab_mark,eval=F}
```{r tab_mark}
data(stuart_tab)
summary(stuart_tab)
```
......
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#' Output of tab_mark function
#'
#' A dataset with the output of tab_mark() function.
#'
#' @format A data frame with 11125 rows and 7 variables
#' \describe{
#' \item{marker}{name of the marker}
#' \item{allele_1}{first allele of the marker}
#' \item{allele_2}{second allele of the marker}
#' \item{n_HM1}{number of homozygous individuals for the first allele}
#' \item{n_HM2}{number of homozygous individuals for the second allele}
#' \item{n_HT}{number of heterozygous individuals}
#' \item{n_NA}{number of non genotyped individuals}
#' }
"stuart_tab"
.Rproj.user/9DAE6990/sources/s-39B546A6/B86C81D8
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......
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......
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......
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......
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