Open wbaopaul opened 5 years ago
Sorry for the late reply! The expected input is a matrix of kmers (rows) vs samples (columns) with the observed frequencies of each k-mer adjacent to the read mapping locations for each sample. This is what is created by the inputKMerFreqs function after having run the Brockman command line tool, which create k-mer frequency vectors for each sample.
I am not clear about what kind of input files I should provided: A cell by peak matrix plus genome sequence? Thanks.