Turn genetic data into
simple conversations

See What You Can Discover

From publication-ready research analysis to personal health insights - what will you uncover?

Fast Analysis, Ready to Publish

Analysis to figures in minutes

Generate volcano plots, run differential expression analysis, and get publication-ready visualizations with statistical corrections applied automatically.

Research Overview

I want to find differentially expressed proteins between my Alzheimer's cases and controls

On it. 30 seconds... [Processing 2,847 proteins] Done. 312 significant hits (FDR < 0.05). Top targets: APP, PSEN1, BACE1 ✓ But TREM2 has the strongest effect (p=1e-12). The immune pathway has several hits.

Run pathway enrichment on those hits

Patient Stratification

Precision medicine ready

Stratify patients by drug response genetics, predict treatment failures before they happen, and match individuals to optimal therapies based on their pharmacogenomic profile.

Research Overview

Stratify my cohort by predicted drug response genotypes

Running pharmacogenomic panel... Done. CYP2C19 (clopidogrel metabolism): 23% poor metabolizers, 54% normal, 23% rapid. SLCO1B1 (statin toxicity): 31% high-risk. CYP2D6 (antidepressant response): 18% poor, 64% normal, 18% ultra-rapid.

Which patients need different treatment options?

Multi-Omics Integration

Genetics meets proteomics

Connect genetic variants to protein expression levels, uncover mechanistic pathways from genotype to phenotype, and build the biological story for your paper.

Research Overview

Correlate genetic variants with protein levels in my cohort

Running cis-pQTL analysis... Done. Found 4 strong effects: TCF7L2 (r=0.68, p=1e-8), PPARG (r=0.54, p=3e-6), FTO (r=0.49), SLC30A8 (r=0.61). Each risk allele increases protein 0.5-0.8 log2 units.

Do these protein changes predict disease risk?


For Personal Use

Supplement Guidance

What you actually need

Understand why standard supplement doses might not be enough for you, and get personalized recommendations based on your metabolism genes.

Personal Overview

Do I need vitamin D supplements?

Analyzing vitamin D pathway... You have risk variants in DHCR7 (rs12785878), CYP2R1 (rs10741657), and GC (rs2282679). Combined effect: your vitamin D levels run 8-10 ng/mL lower than average at the same sun exposure. You're genetically predisposed to vitamin D insufficiency.

Understanding Your Stress Response

How you're wired

Discover why you get overwhelmed more easily than others, understand your stress recovery patterns, and learn why your need for alone time is biological, not a personality flaw.

Personal Overview

Why do I get overwhelmed so easily?

Your data shows variants in stress response genes that affect cortisol regulation. You may have heightened stress sensitivity and slower recovery from social stressors.

Is that why I need so much alone time?

Partly yes. Wh

Your Sweet Tooth

Understand your preferences

Find out whether your sugar cravings are written in your DNA or shaped by your habits. Discover what your taste receptor genes reveal about your sweet preferences.

Personal Overview

Do my genetics give me more of a sweet tooth?

Analyzing your sweet preference genes... Interesting! You're heterozygous for FGF21 (A/G) - you carry both the 'sweet tooth' allele and the 'decreased preference' allele. Your TAS1R2 taste receptors actually suggest decreased sweet food intake. Your genetics don't give you more of a sweet tooth

Why We Built This

"After fleeing Chernobyl and losing family members to cancer, I became a geneticist. But the tools to answer important questions were locked behind technical barriers."

- Alex Kotlar, Founder & CEO

We built Bystro to make powerful genetic analysis accessible to everyone - from researchers advancing science to individuals exploring their own genomic data.

The tools to understand disease didn't exist. So we built them. Now you can focus on the biology instead of debugging code.

Ready to get started?

Join leading research institutions and curious individuals already using Bystro to unlock genetic insights.

We'll send you early access information and setup details.

Research Use Only: This platform is designed for research, educational, and informational purposes. It is not intended for medical diagnosis, treatment decisions, or clinical use. Always consult with qualified healthcare professionals for medical questions and genetic counseling.