A dataset generated by: Input_Example<-QuantumCat(number_of_clones = 4, number_of_mutations = 100, ploidy = "AB",depth = 150, number_of_samples = 2, contamination = c(0,0))
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A list of dataframes
First column containing the name of the sample
The chromosome either 1 2 ... X Y or chr1 chr2 ... chrY
The genomic position of the variant
Number of reads supporting variant allele
Total number of reads (reference + alternative allele) at position
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