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Plasmid Editor

Open a plasmid and work on it in the view that suits the task: the circular map for the whole construct, the linear map for a region, the sequence view for individual bases. Annotations, cut sites, translations and open reading frames are all computed from the sequence in front of you and update as you edit it.

Nine real annotation files: GFF3 · GTF · BED · EMBL across three divisions and three molecule types, the 5′-UTR introns most parsers have never met, and the JBEI registry’s own XML

01

What it does

  1. 01Circular, linear and sequence views of the same molecule
  2. 02Feature, part and primer annotation editing, with type and direction
  3. 03Six-frame translation and automatic open reading frame detection with a settable minimum size
  4. 04Restriction cut sites drawn on the map, filtered to single cutters when needed
  5. 05GC content and composition statistics, updated live
  6. 06Search across bases, features, enzymes and positions
  7. 07Undo and redo over sequence and annotation edits
  8. 08Import and export across GenBank, FASTA, EMBL, GFF3, GTF, BED, SnapGene and more
02

What it runs on

Every sequence operation runs in the browser against the open document, so a map, a digest and a translation always describe the same molecule rather than a saved snapshot.

Everything runs client-side. Files are parsed in the browser and projects are saved on this machine, so an unpublished sequence is never uploaded.

03

Questions

Can it open SnapGene .dna files?
Yes. SnapGene files are parsed in the browser, including the embedded construction history where the file carries one.
Are my sequences uploaded?
No. The application is local-first: files are parsed in the browser and projects are saved on the machine.

Also searched as

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