Genomics, back in your hands.

Omabit is an AI platform for genomic analysis. Upload your sequencing files, ask questions in plain English, and get publication-ready results. No pipeline engineering required.

Use Omabit if you're a

• Biologist sitting on sequencing data you can't analyze alone
• Researcher with a question and no bioinformatician to call
• Computational scientist who wants to move 10x faster

Used in active drug discovery workflows at clinical-stage pharma companies.

Interactive Demos - Try Them Below!

You have a VCF file with genetic variants and a phenotype file with patient outcomes. Click a model below to run a genome-wide association study and find which variants predict drug response.

You have two datasets with different ID formats — a common headache in genomics. Omabit figures out which columns match across files and merges 148 million rows in seconds. Pick how you want to combine them below.

You have clinical trial data. Omabit suggests relevant plots — click one to visualize your data instantly.

You have a list of variants. Omabit pulls in clinical significance from ClinVar, population frequencies from gnomAD, and pathogenicity scores — then lets you explore gene interaction networks.