Hi everybody, I'm currently working on somatic mutations at diagnosis in leukemia with a panel of 81 genes tested at diagnosis (I have data on the type of mutation, the VAF and there is also copy number variation evaluation) of 70 patients. How do you suggest to organize data in excel to evaluate them? which graphics do you suggest to realize?

This is the first time that I manage NGS results with a panel of 81 genes + CNV and I'm a little lost.

Thank you.

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