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Hi Rute,

For Sanger sequencing typically you would look at the Chromatograms. Here is a nice webpage that provides additional details.

https://seqcore.brcf.med.umich.edu/sites/default/files/html/interpret.html

If you goal is to view a chromatogram to view ab files and assess SNP calls from Sanger sequencing, there are a variety of free tools (genestudio, Sequence Scanner, 4 peaks, etc…).

Kind Regards,

-Steve