Entering edit mode
9.7 years ago
stefan.mester
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0
Hey there,
thanks a lot for the great software, I like it a lot and use it extensively to analyze my whole genome sequence NGS data, so far mainly for SNPs and copy number variations.
My question is: how do you guys cope with structural variants such as inversions and translocation. can the software handle these inputs and where do you specify the VarType
best regards and many thanks in advance
Stefan
