Agentic RNA-seq analysis

From a plain-English goal to a reproducible RNA-seq pipeline.

Omixgen turns a natural-language description and your sequencing files into a validated, executable bioinformatics workflow — planned by an LLM, reviewed by you, and run with full provenance.

See how it works
FastQCMultiQCTrimmomaticHISAT2 samtoolsfeatureCountsDESeq2

What is Omixgen?

Omixgen is an agentic platform for bulk RNA-seq. Instead of hand-writing shell scripts and wiring tools together, you describe the outcome you want. Omixgen parses your inputs, plans a workflow from a catalog of real bioinformatics tools, compiles it to readable Python, and — only after you approve the exact code — executes it and renders the results. Every intermediate object is inspectable and logged.

What it can do

Natural-language planning

Describe your objective in plain English; Omixgen designs a valid, ordered workflow.

Human-in-the-loop approval

Review the plan and the exact compiled code. Nothing runs until you approve it.

Real bioinformatics tools

QC, trimming, spliced alignment, quantification and differential expression — FastQC to DESeq2.

Transparent & reproducible

Each step compiles to readable Python and is provenance-logged for a full audit trail.

Rich results overview

QC reports, plots and DEG tables rendered inline, with one-click downloads.

Fully inspectable

Task spec, plan, script, executor I/O and a live timeline — all in one logs panel.

How it works

  1. 1

    Describe

    Add your files and state your goal.

  2. 2

    Plan

    The agent drafts and validates a workflow.

  3. 3

    Approve

    Inspect the plan and exact code, then approve.

  4. 4

    Execute

    Omixgen runs the compiled pipeline.

  5. 5

    Review

    Explore results, reports and downloads.

Ready to run your first analysis?

No setup in the browser — just describe your goal and go.