Pick a chassis and a target gene; get ranked sgRNA candidates with PAM, activity score, and off-target risk, plus left/right homology arms.
From a chassis and a target site to a complete CRISPR editing plan, five stages annotate each step in this entry.
Choose from a 30-strain chassis library spanning bacteria, yeast, and filamentous fungi.
Find a gene by name or keyword, list repeat elements, or paste a bare DNA sequence.
Scan for PAM, score on-target activity, and rank off-target risk per candidate.
Build left/right arms with copy-number and PAM-disruption checks.
Copy sgRNA ordering format and download homology-arm FASTA.
Bacteria, yeast, and filamentous fungi, each with strain-specific genome annotations.
Rank guides by Azimuth score and flag MM0/MM1/MM2+ off-target hits.
Synonymous-mutate PAM sites inside the arms to prevent Cas9 re-cutting.
Default and recommended homology-arm lengths tuned per chassis.
Pick a chassis, name a target gene (or paste a sequence), then design.
Watch the design advance stage by stage.
The ranked sgRNA candidates and the left/right homology arms with copy-number and PAM-disruption notes.
Each saved run becomes a reproducible entry with an Entry ID you can cite in your methods. Handoff to the Expression Cassette Designer prefills the guide sequence.
Run the design first, then save it here.