Secondary Analysis
Alignment, variant calling, and quality control run automatically on elastic cloud compute — no infrastructure to manage.
200+ Research Labs Who Trust Our Genomic AI
Your genome is a three-billion-letter story. Our AI reads every line — surfacing the variants that matter and turning years of analysis into days. Let precision genomics drive your next discovery.
What is Strand
Strand is a precision-genomics platform that turns raw sequencing data into clinical-grade answers. Where legacy pipelines take weeks of manual curation, our models read every base pair, flag the variants that matter, and explain why — so your team spends its time on discovery, not on data wrangling.
The Platform
Every stage of genomic analysis, unified in a single AI-native workspace.
Alignment, variant calling, and quality control run automatically on elastic cloud compute — no infrastructure to manage.
Large models translate each variant into plain-language clinical context — with citations you can trace back to source literature.
Cross-reference ClinVar, gnomAD, and OMIM in real time, so every call arrives pre-annotated with population frequency and pathogenicity.
Benchmarked against Genome in a Bottle truth sets and revalidated on every release, so precision never quietly drifts.
End-to-end encryption with HIPAA, GDPR, and ISO 27001 controls. Genomic data never leaves your region without consent.
Share cohorts, comment on variants, and hand off cases across your team — with a full audit trail on every decision.
Research
From rare-disease diagnostics to population-scale studies, Strand powers work that can't afford to be wrong.
“Strand collapsed our variant-interpretation backlog from months to an afternoon. It's the first tool our clinicians actually trust to show its reasoning.” Principal Investigator, rare-disease genomics program
Pricing
Transparent per-genome pricing. No sequencing lock-in, no surprise compute bills.
Researcher
For individual scientists exploring their first datasets.
$0/ month
Lab
For teams running production analysis pipelines.
$499/ month
Enterprise
For clinical and population-scale genomics programs.
Custom
Help & FAQ
Everything you need to know about running your data through Strand.
Strand ingests FASTQ, BAM, CRAM, and VCF files directly. Upload from your local machine, an S3/GCS bucket, or stream straight from your sequencer. We handle both whole-genome and targeted-panel data.
All data is encrypted in transit and at rest, isolated per organization, and processed within your chosen region. We maintain HIPAA, GDPR, and ISO 27001 controls, and your data is never used to train shared models.
Our variant-calling pipeline is benchmarked against Genome in a Bottle reference materials at 99.9% concordance and revalidated on every release. Enterprise deployments support CLIA/CAP workflows with full documentation.
Yes. GRCh38 and T2T-CHM13 are supported out of the box, and you can supply custom references, target regions, or drop in your own analysis steps through the API and workflow editor.
Pricing is per genome analyzed per month, with compute included — no separate cloud bill. Unused capacity doesn't roll over, and Enterprise plans move to committed-volume pricing.