dna-seq on GitHubJust-DNATry the demo

Your genome, read
on your own computer.

See what published studies say about your DNA, without uploading it.

Try the demoInstall it
One line of your genome file
chr6 108587315 G T 0/1
Longevity Maprs2802292

FOXO3

Your genotype G/T

Protective
4 studiesAnton Kulaga’s public genome

Studies come in. Your file stays.

Your computerNothing inside this line is uploadedPublished studiesPapers and ClinVarClinPGx and CPICThe PGS CatalogModule catalog24 modules, onetopic eachA sequencing service2Just-DNA-Litereads it with themodules you chose1Your genome filea VCF file3Your reportwith the studiesbehind each findinginstallyou download itread here

  1. Get your genome file

    From a sequencing service, as a VCF.

  2. Open it in Just-DNA-Lite

    Free, on Linux, macOS or Windows.

  3. Read your report

    Each finding names its studies.

This is the app.

It cleans up your file and shows what it kept before anything is matched.

Polygenic scores, annotated files and reports each have a tab of their own.

What a report shows
The Just-DNA-Lite Annotation page for antonkulaga.vcf: tabs for Input, Polygenic Risk Scores, Annotated Files, Reports and Analysis Tools, the quality filters applied, and the first rows of the normalized VCF.
Anton Kulaga's public genome after upload: the quality filters kept 4,257,537 of 6,079,744 variants.

What you can read about yourself

See a full report before sequencing.

The demo holds two public genomes, so every module runs on real data.

Open the demoInstall it

Writing a module? Start at Contribute. Building software? See Developers.

Watch the video tutorial