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Hello there, I am using indigo to call variants from sanger sequencing chromatograms and I noticed that the app outputs 3 alignments and a bcf file containing variants from all alignments. I want to keep only variants from the alignemnet with the highest score, is it possible ?
The text was updated successfully, but these errors were encountered:
Hello there, I am using indigo to call variants from sanger sequencing chromatograms and I noticed that the app outputs 3 alignments and a bcf file containing variants from all alignments. I want to keep only variants from the alignemnet with the highest score, is it possible ?
The text was updated successfully, but these errors were encountered: