This package has 3 main functions that all centre on analyzing the genotypes of cancer cell lines and compares them against 1,497 unique cancer cell lines analyzed across 3 large pharmacogenomic datasets. The 3 functions are to 1) identify an input cell line VCF using the genotype and B-allele fraction (BAF) as the input for a logistic regression, 2) identify regions of the genome that are drifted by scanning for segments where the BAF are significantly different from a comparator cell line, and 3) run a deconvolution on the cell line BAFs using NMF to identify if two or more cell lines are mixed and to what proportion they are.
|License||MIT + file LICENSE|
|Package repository||View on GitHub|
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