The GenomeAdmixR package provides many different visualization options, here we will explore a variety of them. First, we simulate a scenario with selection, to obtain somewhat meaningful results.

```
select_matrix <- matrix(nrow = 1, ncol = 5)
select_matrix[1, ] <- c(0.5, 1, 1 + 0.05, 1 + 0.1, 0)
population <- simulate_admixture(
module = ancestry_module(markers =
c(0.5,
seq(0, 1, length.out = 100))),
pop_size = 1000,
total_runtime = 200,
select_matrix = select_matrix)
```

`## Found a selection matrix, performing simulation including selection`

Now, we can first view whether selection on our marker has yielded an increase in frequency:

`plot_over_time(population$frequencies, focal_location = 0.500)`

Indeed, we observe that over time the frequency of the allele under selection (0) increases to fixation due to selection.

How are the alleles scattered across the genome? we can answer that with the function plot_frequencies:

`plot_frequencies(population, locations = seq(0, 1, length.out = 1000))`

As expected, we observe a huge increase around the location of the marker under selection (at 0.5 Morgan).

If instead, we are interested in the change in frequency of a marker, we can do so using plot_difference_frequencies.

`plot_difference_frequencies(population)`