Whole-plasmid sequencing: consensus vs design
Compare a whole-plasmid sequencing CONSENSUS (the single circular FASTA a nanopore plasmid service returns) against the design it was supposed to be, and say whether they are the same molecule. Finds the rotation and strand itself — an assembler starts the circle wherever it landed and half the time returns the reverse complement, so the two almost never line up as written — then reports every difference in the DESIGN's own coordinates. Each difference carries the length of the identical-base run it sits in, because a 1 bp indel inside a homopolymer is both the commonest long-read basecalling artefact and what a real slippage mutation looks like, and a bare difference list cannot tell them apart. Pass the design as an annotated GenBank record and every difference is also read against its features: silent, missense with the codon number, or a premature stop. Complements sequencing_readback_verify, which aligns raw READS through minimap2; this one needs no reads and no sidecar.
Batchable via POST /batch.
Request
- Base URL: https://seqbench.com/api/v1
- URL: https://seqbench.com/api/v1/whole_plasmid_verify
- Auth: none required
Request body
Response
Tool ran successfully.
Example response
{
"provenance": {
"apiVersion": "1.1.0"
}
}Changes
No recorded changes to this operation across all 1 revision of this API.