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sciClone input LOH

Dear all,

I want to use sciclone on my somatic variant data. I am confused about the input it takes. One is the CNA information but incase of LOH input file, Is it cnLOH or LOH ? what i mean is looking at the results from ASCAT, should i give regions where we have major 2n and monir 0, or all the regions where the minor is 0 with major allele could be 2n, 3n trisomies, so on etc...

Can anyone explain what LOH files mean here in context of sciclone input?

Thanks in advance.

sciclone input loh

Yep, that's the definition you're looking for. Hope it cleared things up!

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