The tool for parse ab1 file and identification of unknown indels, online and free!


Sequence-specific nuclease-based genome targeting systems, i.e., TALENs and CRISPR/Cas9, often cause uniform biallelic and heterozygous mutations in diploid organisms. Direct sequencing of PCR products containing such mutations results in superimposed sequencing chromatograms. This tool serves to decode automatically sequencing chromatograms with biallelic, heterozygous, and homozygous mutations into allelic sequences.
For testing the program, two sequencing ab1 files and the corresponding references are provided.

Step 1

Upload a chromatogram (*.ab1) file

Example block-level help text here.

Step 2

Enter an intact reference sequence, if you only need to view the peaks, please keep this blank.