Kmeggie+Simplifying the code of life

Sequencing QC for laboratories worldwide

Your sequencing run is done.
Can you trust the file?

Kmeggie+ checks your FASTQ data before anyone builds on it. In your browser, on your own machine, in minutes.

Early-stage prototype built in Kenya. Browser-based validation and QC reporting work today; a command-line workflow is in development. Not a validated diagnostic tool.

Illustrative image

How it works

Three steps between the sequencer and a decision.

01

Bring the file

Drop a FASTQ file, compressed or not, into the browser. It stays on your machine. Nothing is uploaded.

02

We check it

Structure first: every record well formed. Then quality: base scores, composition, read lengths, duplicates, and N content.

03

Read the report

Clear pass, review, and low-quality flags with the reasoning behind them, and an HTML report you can share with the team.

See everything the product does →

Try it here

Follow a sequencing file.

A two-minute walkthrough of what Kmeggie+ does to a file, using synthetic data so there is nothing to upload.

Open the full demo →
How to use this walkthrough
  1. Pick a sample below: clean reads, or reads whose quality drops toward the end.
  2. Step through the four stages with the buttons, or click a stage directly.
  3. Switch samples at any stage to see how the same checks read a different file.
What the full demo adds
  • Bring your own file: .fastq, .fq, or .gz, up to 50 MB and 200,000 reads.
  • Charts for base quality, composition, and read length, plus every validation check.
  • Export the report as a standalone HTML file. Your data never leaves the browser.
Choose a sample

Step 1 of 4

Synthetic demonstration data, analysed by the prototype's local engine.

Pilot interest

Help us test Kmeggie+ against real laboratory conditions.

We are preparing discovery and pilot work with public-health and genomics laboratories. If that sounds like your lab, tell us about it.