About DNAObs

Transforming genetic data into meaningful insights

Genome Interpretation Studio

Unlock the StoryWithin Your DNA

DNAObs transforms your existing genome data into actionable insights, ancestry narratives, and health intelligence. We interpret, not sequence.

See How It Works

12K+

Genomes Analyzed

And growing daily

700K+

Genetic Markers

Comprehensive coverage

2,000+

Ancestry Populations

Global reference data

150+

Health Traits

Actionable insights

$15

Expert Review

Optional scientist verification

100%

Data Ownership

Your genome, your control

Live Preview

See Your Analysisin Action

Experience what your personalized genome dashboard looks like with interactive charts, risk assessments, and ancestral insights.

DNAObs Analysis Dashboard
Live

687,421

SNPs Analyzed

156

Health Markers

12

Risk Factors

48

Traits Found

Ancestry Breakdown

Origins

Health Risk Assessment

Cardiovascular25%
Neurological45%
Metabolic15%
Immune65%
Cancer30%

Haplogroup Analysis

Discover your paternal and maternal lineage with high-confidence haplogroup identification.

Paternal (Y-DNA)

R1b-M269

Western European lineage • 98.5% confidence

Maternal (mtDNA)

H1a1

Mediterranean origin • 96.2% confidence

Trait Insights

Explore genetic markers for physical traits, wellness factors, and lifestyle tendencies.

Eye Color

Brown/Hazel

High confidence
Caffeine

Fast Metabolizer

High confidence
Lactose

Tolerant

Medium confidence
Sleep Type

Night Owl

High confidence

Ancestry Migration Map

Visualize your ancestral origins and migration patterns across the globe with interactive markers.

29%22%16%12%
Affinity:
Low
Medium
High
N
1Italy
28.5%
2Germany
22.3%
3Ireland
15.8%
4France
12.4%
5Poland
8.2%
6Greece
5.7%
7Spain
4.1%
8United Kingdom
3.0%

Health Risk Indicators

Clear, color-coded risk stratification helps you understand your genetic predispositions at a glance.

Cardiovascular - Low RiskType 2 Diabetes - ModerateAlzheimer's - Low RiskBRCA1 - Protective VariantCeliac Disease - Low RiskMacular Degeneration - Moderate
Your Personal Command Center

What Your DashboardContains

Access powerful tools designed to make your genome data understandable, actionable, and truly yours.

DNA Analysis Hub

Dive into your personalized genome insights with interactive visualizations and evidence-backed recommendations tailored to your unique genetic profile.

Trait Deep-DivesHealth MarkersContinuous Updates

DNA Programs

Explore specialized programs crafted by genomic experts to accelerate performance, longevity, and cognitive resilience based on your DNA.

Guided ProtocolsExpert FrameworksAdaptive Pacing

Ancestry & Origins

Discover your ancestral journey with detailed migration timelines, haplogroup analysis, and regional breakdowns backed by peer-reviewed research.

Migration MapsHaplogroupsRegional Analysis

Health Intelligence

Access comprehensive health reports including pharmacogenomics, carrier status, and wellness markers to make informed decisions with your healthcare team.

PharmacogenomicsCarrier StatusWellness Signals

Account & Security

Manage your profile, privacy controls, and notification preferences from a single streamlined hub with enterprise-grade security.

Privacy ControlsProfile SyncMFA Protection

DNAObs Dispatch

Stay ahead with exclusive case studies, new feature drops, and research-backed breakthroughs curated exclusively for members.

Insider BriefingsPriority AccessWeekly Intel
DNA Analysis Studio

Comprehensive Genome Intelligence

Upload your raw DNA data from any provider and receive actionable risk tiers, haplogroup calls, and exportable evidence—all processed locally for complete privacy.

Six Powerful Analysis Modules

Overview

Summary dashboard with key findings at a glance

Ancestry

Paternal & maternal haplogroups with migration maps

Cancer Risk

Inherited cancer markers with risk stratification

Health Insights

9 categories of health markers and conditions

Traits

Physical, wellness, and behavioral trait analysis

Export

Download JSON reports for clinician handoff

9 Health Insight Categories

Mitochondrial
Neurological
Cardiovascular
Metabolic
Immune System
Hematological
Endocrine
Musculoskeletal
Developmental

Trait Analysis Categories

Physical Traits

Eye color, hair type, freckling

Wellness

Caffeine metabolism, lactose tolerance

Nutrition

Vitamin absorption, taste perception

Disease Risk

Genetic predispositions

Behavioral

Sleep patterns, circadian rhythm

Ready to Analyze Your DNA?

Upload your 23andMe, AncestryDNA, or raw genotype files (.txt, .csv, .tsv) and get instant results. All processing happens locally—your data never leaves your browser.

Learn More
Zero data retention
Local processing
Export JSON reports
Why DNAObs

Interpretation-First Philosophy

We are not a lab. We do not collect samples. We focus on one thing: making your existing genome data meaningful through expert interpretation and beautiful visualization.

Interpretation-First Approach

We focus on making sense of your genome data, not running lab tests. Pure intelligence and storytelling from your existing data.

Visual Storytelling

Complex bioinformatics transformed into intuitive visualizations, migration timelines, and ancestry word maps you can understand.

Consent-Driven Analysis

Every analysis starts only after you approve. You decide what questions we explore and how your data is used.

Global Expertise

Expert teams bringing diverse genomic perspectives and cutting-edge research to deliver actionable insights.

Interactive Dashboard Preview

Trait Graphs

Ancestry Breakdown

Migration Maps

Premium Upgrade

Expert Scientist Verification

For just $15, upgrade to receive a personalized review from a dedicated genomics scientist.

Manual Verification

Your results are personally reviewed and verified by a genomics expert

Detailed Interpretation Letter

Receive a comprehensive written analysis explaining your key findings

Direct Q&A Access

Ask questions directly to clarify findings and discuss implications

$15

One-time upgrade

Dedicated genomics scientist
Personalized interpretation
Medical consultation ready
Direct Q&A support
Trusted by Experts

What Our Partners Say

DNAObs turned a dense genome file into visuals our care team used to guide preventive decisions. The clarity is remarkable.

D

Dr. Lena Ortiz

Clinical Geneticist, Meridian Health

The ancestry word map resonated with our community and backed every claim with referenced data. Truly groundbreaking work.

A

Amir Khalil

Director of Genomics, HelixCore Research

Finally, a platform that respects data sovereignty while delivering actionable insights. Our patients love the experience.

D

Dr. Sarah Chen

Precision Medicine Lead, Pacific Health

Got Questions?

Frequently Asked Questions

All genomic workloads are encrypted in transit and at rest using AES-256 encryption. DNAObs aligns with HIPAA, GDPR, and regional genomic data regulations. Your DNA analysis is processed locally in your browser—we never store or retain your genetic data on our servers.

No. DNAObs is not a lab. We interpret genome data you already have from providers like 23andMe, AncestryDNA, or clinical sequencing. Simply upload your raw data files (.txt, .csv, .tsv, VCF, BAM/CRAM, or FASTQ) and receive instant analysis.

Your analysis includes 6 modules: Overview (summary dashboard), Ancestry (Y-DNA & mtDNA haplogroups with migration maps), Cancer Risk (inherited markers with risk stratification), Health Insights (9 categories including neurological, cardiovascular, metabolic), Traits (physical, wellness, nutrition, behavioral), and Export (JSON reports for clinician handoff).

For an optional $15 upgrade, a dedicated genomics scientist personally reviews your results, prepares a detailed interpretation letter, verifies key findings, and provides direct Q&A support. This is perfect for medical consultations or important personal discoveries that require professional verification.

Basic analysis completes instantly since all processing happens locally in your browser. For complex interpretations or Expert Scientist Review, results are typically ready within 2-5 days. You'll receive interactive dashboards, variant graphs, and downloadable JSON reports.

We support raw data exports from major providers (23andMe, AncestryDNA, MyHeritage) as well as VCF, BAM/CRAM, and FASTQ files from clinical sequencing. Maximum file size is 50MB. All common genotype formats (.txt, .csv, .tsv) are supported.

Our reports are designed to inform conversations with healthcare providers. For medical decisions, we recommend the Expert Scientist Review ($15) and consultation with a licensed genetic counselor or physician. We provide risk stratification but do not diagnose conditions.

Ready to DiscoverYour Genome Story?

Join thousands who have transformed their raw DNA data into meaningful insights. Sign up today and start your journey.

Talk to an Expert
HIPAA Compliant
SOC2 Certified
2-5 Day Turnaround