jean — Molecular Biology & Genomics
by FastDrop
Validated molecular biology tools: cloning, primers, CRISPR, Sanger, alignment, qPCR, phylogenetics
Validated molecular biology tools: cloning, primers, CRISPR, Sanger, alignment, qPCR, phylogenetics Official MCP Registry: io.github.genmnz/jean@1.0.1. Remote endpoint: https://jeanslabs.vercel.app/mcp
Problem it solves
Discoverable MCP server listed in the official MCP Registry.
How it's different
Remote MCP endpoint ingested from the official registry and probed by FastDrop.
Ingested from the official MCP Registry
FastDrop pulled this entry from the official MCP Registry as io.github.genmnz/jean and probed the endpoint. The maker did not submit it, so the outbound link is not endorsed
and the description is not theirs.
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Read directly from the endpoint on 20 Oct 2026. Not supplied by the maker.
list_workflow_templatesThe built-in starter workflows — id, name, what each does and which tools it chains. Pass an `id` to get that template’s graph back, ready to hand to `run_workflow`. This server is stateless, so these
validate_workflowWould this workflow graph run? Returns the blocking errors — an unknown tool, a wire into a port that does not exist, a cycle — each naming the node and the port, without running anything.
run_workflowRun a workflow graph: nodes naming tools, wires carrying one node’s output into another’s input, `$whenExpression` to make a step conditional, and `scatter` to run a step once per element of a list. R
get_open_recordReturn the plasmid/sequence currently open in the editor. Emits it as a `record`, so it is the SOURCE node of a pipeline — wire its record into any downstream node's $subject.
load_recordRead a CHOSEN project document as a record — the pipeline's data-reader source, for running on a specific file instead of whatever happens to be open in the editor. Wire its `record` into any downstre
list_libraryList the project's sequence documents (id, name, length, topology, kind).
find_restriction_sitesCut positions of the given enzymes on the open plasmid (top/bottom cut, overhang, kind).
find_star_sitesWhere the given enzymes could ALSO cut the open plasmid under non-standard conditions, from REBASE's own star-activity list and its one-base rule. Not cut sites: these need low ionic strength, high pH
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