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AI agent for microbiologists

DNA Construct Design Check Agent

Constructs that are correct by design and confirmed by sequencing

DNA Construct Design Check Agent: what goes in, what the agent does and what you get

What it does

A single base error in a construct design can cost weeks of lab work. Before ordering, this agent reads your construct map and translates the open reading frame, comparing it with the intended protein. It checks start and stop codons, tag placement and linkers, and looks for restriction sites that would cut the insert. It checks primer binding and melting temperatures and flags rare codons for the chosen host. Each problem gets a suggested fix, such as a silent change or a new primer, and it rechecks the revised design. The scientist approves every order. When sequencing comes back, it aligns the reads to the design and lists any differences. If the clone does not match, it suggests picking another colony. Edge case: a silent mutation added to remove a restriction site is accepted only if it does not create a rare codon.

How it works

Follow the arrows from top to bottom. The orange dashed arrow is the loop: when a check fails, the agent goes back and tries again.

Start and resultWhat it doesA check on its own workWaits for your OKGoes back and retries
Yes, continueApprovedYes, continueNoNo 1 STARTS WHEN Construct design marked ready 2 USES A TOOL Translate the reading frame and compare with theintended protein 3 DOES Check tags, restriction sites, primers and codon use 4 CHECKS THE RESULT Is the design free of errors? If not: suggest fixes such as silent changes or newprimers, then recheck. Back to step 2. 5 YOU APPROVE Scientist approves the order 6 USES A TOOL Align sequencing reads to the design 7 CHECKS THE RESULT Does the sequenced clone match the design? If not: list differences and suggest picking anothercolony. Back to step 6. 8 RESULT Verified construct recorded
Read the steps as a list
  1. Construct design marked ready
  2. Translate the reading frame and compare with the intended protein
  3. Check tags, restriction sites, primers and codon use
  4. Is the design free of errors?If not: suggest fixes such as silent changes or new primers, then recheck. Back to step 2.
  5. Scientist approves the orderThe agent waits here for your OK.
  6. Align sequencing reads to the design
  7. Does the sequenced clone match the design?If not: list differences and suggest picking another colony. Back to step 6.
  8. Verified construct recorded

How it decides

A design passes when it translates to the intended protein, keeps tags in frame, has no unwanted sites for the cloning method and primers meet the set limits.

  • Flag internal sites for the enzymes in the cloning method
  • Flag rare codons for the host above the set count
  • Accept a clone only when coding regions match fully

Make it yours

Every agent is a starting point. You choose these settings for your own situation.

  • Host organism
  • Restriction enzymes in use
  • Primer melting temperature range
  • Rare codon limit

What keeps you in control

It always asks you first

  • Ordering synthesis or primers

Hard limits

  • Never orders without approval
  • Never edits the master design file

It stops when

  • Done: clone verified
  • Stop: design incomplete or intended protein missing; ask the scientist

Set it up

We guide you through the set-up, step by step

Members get the full set-up guide for this agent. No technical skills needed: you copy, paste and upload.

10 minto set it up in your AI
5 AIsChatGPT, Claude, Copilot, Gemini, Grok
  • One set of instructions to paste into your AI, with the clicks for ChatGPT, Claude, Microsoft 365 Copilot, Gemini and Grok
  • The agent then walks you through connecting your own data, one source at a time
  • A downloadable copy with the flow chart, the rules and the full guide
Get access to this agent

An example run

What happensA design for a His-tagged enzyme had a one-base deletion after the tag that shifted the frame. The error check failed, and the agent suggested restoring the base. The recheck passed, and the scientist approved the order. Sequencing of colony 1 showed a point mutation at base 412, so the match check failed. The agent suggested colony 2, which matched the design fully.

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