[svtoolkit-help] A suggestion or question for the input file

[lishiyong <lis...@bg...>]

Hi:
I have 22 samples(11 tumour samples and 11 matched adjacent non-tumour samples). Each sample has been sequenced almost 50X whole genome. I want to use the genome-strip to detect the SV. But it would take too much time to merge into one bam,and too much memory to storage the bam. Could it get a list of each sample's bam as the input? or is There another way to solve this problem?

Best wishes to you.
Shiyong li