DNAScale
Chromatogram

Look at your sequences, then trust them.

Open Sanger trace files, align reads to a reference, and walk every difference with the raw chromatogram right underneath.

Drop files here
.ab1 / .scf.fasta / .fastq.gb.aln.dnascale
1Open readsTrace files are trimmed by quality automatically and reverse reads are flipped to match.
2AlignMap reads to a reference, or build a multiple alignment of anything.
3VerifyJump from difference to difference with the chromatogram centred on each base.
Drop to add sequences & traces