Hello RG,

I have results from Sanger sequencing for validation of multiple variants I have found in my patients cohort, can you please instruct me if there is some sort of open source program that I can use to compare the results quicker? So far I have only used manual inspection with FinchTV and Word, but that will take forever for a 100+ variants to check...

I am a beginner/intermediate with R but don't know Python.

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