Upload a VCF file and watch AI annotate every variant — ClinVar lookup, pathogenicity score, population frequency, clinical summary. Try it right now, no account needed.
Try the Demo →Traditional genomic analysis requires a team of specialists and days of manual work. Baseshift compresses the entire workflow into an autonomous agent that processes, analyzes, and reports.
Drop in your VCF or VCF.GZ file. We handle the rest — no bioinformatics setup, no configuration.
Every variant cross-referenced against ClinVar, gnomAD, and OMIM. Pathogenicity scored, gene names resolved, population frequencies attached.
Auto-generated report with ranked findings, actionable variants highlighted, and shareable summary. Ready to act on immediately.
Designed by scientists who have spent years at the bench. Every feature exists because manual analysis demanded it.
Works with data from any major sequencing platform. No vendor lock-in. Upload from Illumina, PacBio, Nanopore, or BGI.
Watch your analysis run in real time. No black boxes, no overnight batch jobs. Results stream as they're computed.
AI cross-references every variant against clinical databases, published literature, and population studies for context.
Clinical-grade reports generated automatically. Variant tables, pathogenicity scores, and actionable findings in clean, shareable formats.
No subscriptions, no seat licenses, no upfront commitments. Pay only for the samples you analyze.
First sample analysis is free. No credit card required to start. After that, your first 100 samples are half off — automatically.
First sample free. Then $7.50/exome during promo.
$15 standard after 100 samples. No subscription.
Every day, sequencing data sits waiting for a specialist who's backlogged for weeks. Baseshift eliminates that bottleneck. Upload your VCF, get a full clinical report in minutes.