Hello,

I have two questions regarding cnv analysis using CytoscanHD data.

1)

I am currently implementing PSCBS on my Cancer datasets. This tool looks 
quite interesting to me.

However, what to do you say about giving exact values for calling copy 
number gains and losses? Can  you suggest any thresholds? Any values above 
4 would be high copy gains and near zero would be deletions?

I have a dataset of more than 200 hundred lung cancer samples so I want to 
apply significant testing on cnvs. Does GISTIC type algorithms will work on 
the attached example file? Or any other method you suggest


2)

Is tumorboost works with cytoscanHD data?

Thanks 

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