Tidying input by Chr Start
1 | Tidy_output(r, Genotype_provided, SNV_list)
|
r |
output from Cluster_plot_from_cell |
Genotype_provided |
If the FREEC_list is provided, then should be FALSE (default), otherwise TRUE |
SNV_list |
A list of dataframes (one for each sample), with as columns : (for the first column of the first sample the name of the sample), |
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