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I too wonder what input is used by absCNSeq. I used copy number calls from varscan2 as input to DNAcopy, generated smoothed segments and merged them. You mentioned segment2CNV2.R is the input in Issue #1 . What is the input for segment2CNV2.R? Rather, what are the steps I need to follow to correctly feed data to absCNSeq?
Thanks.
The text was updated successfully, but these errors were encountered:
Hi,
I too wonder what input is used by absCNSeq. I used copy number calls from varscan2 as input to DNAcopy, generated smoothed segments and merged them. You mentioned segment2CNV2.R is the input in Issue #1 . What is the input for segment2CNV2.R? Rather, what are the steps I need to follow to correctly feed data to absCNSeq?
Thanks.
The text was updated successfully, but these errors were encountered: