I did Sanger Sequencing on 10 samples targeting one specific gene to see whether we detect a particular SNP. We did forward, reversed and tested three primer sets so there are quite a lot samples in total.
Now, I am wondering if there is a quick way to generate chromatograms of the data so for all the 10 samples, aligned to the reference genome? This would save a lot of time compared to the conventional way (aligning via Blast ect.).