30× WHOLE-GENOME SEQUENCING
One sample. A genome you can keep using.
Start with complete sequencing, then choose the report scope and turnaround that fit your needs. Every option preserves standard genomic files and states its service scope clearly.
At-home cheek swabDownloadable standard filesStripe, Alipay & WeChat Pay
Current storeOther countries · independently configured prices and shipping
Choose a Bundle
One complete genome. Different report scopes and turnaround times.
Current bundle prices are shown below. Currency, sample arrangements, and order details appear before payment.
Compare 47 items below. Swipe horizontally on mobile to see all four bundles.
| Compare | Sequencing Only · 7–8 Weeks | Standard Bundle · 7–8 Weeks | Expedited Bundle · 4–6 Weeks | Ultra Rapid Bundle · 2–3 Weeks | Build Your Own Bundle |
|---|---|---|---|---|---|
Genome Sequencing Only WGS Bundle Checking your account… 30× WGS and standard genome files. Analyses sold separately. Please wait | Rare Disease & Carrier Screening WGS Bundle Checking your account… 30× WGS; cheek swab kit; basic health and carrier screening Please wait | Comprehensive Health Screening WGS Bundle Checking your account… Everything in Standard; broader health screening Please wait | Professional Health Screening WGS Bundle Checking your account… Everything in Comprehensive; professional health screening Please wait | Custom WGS Bundle Checking your account… Start with 30× WGS; choose reports and turnaround Please wait | |
| WHAT’S INCLUDED | |||||
| 30× Whole Genome Sequencing | ✓ | ✓ | ✓ | ✓ | ✓ |
| Standard Genome Files | ✓ | ✓ | ✓ | ✓ | ✓ |
| Estimated Turnaround | 7–8 weeks | 7–8 weeks | 4–6 weeks | 2–3 weeks | Confirm on request |
| Reports / Health Areas | 0 (purchase from App Store) | 5 items | 10 items | 20 items | Choose as needed |
| HEALTH AREAS & REPORTS | |||||
| Genetic Health Screening | — | ✓ | ✓ | ✓ | Choose as needed |
| Carrier Screening | — | ✓ | ✓ | ✓ | Choose as needed |
| Connective Tissue Disorders | — | ✓ | ✓ | ✓ | Choose as needed |
| Autoimmune Disorders | — | ✓ | ✓ | ✓ | Choose as needed |
| Developmental Disorders | — | ✓ | ✓ | ✓ | Choose as needed |
| Heart Health | — | — | ✓ | ✓ | Choose as needed |
| Brain Health | — | — | ✓ | ✓ | Choose as needed |
| Medication & Drug Response | — | — | ✓ | ✓ | Choose as needed |
| Reproductive & Hormonal Health | — | — | ✓ | ✓ | Choose as needed |
| Cancer Risk | — | — | ✓ | ✓ | Choose as needed |
| Nervous System Health | — | — | — | ✓ | Choose as needed |
| Gut Health & Digestive Disorders | — | — | — | ✓ | Choose as needed |
| Metabolic & Endocrine Health | — | — | — | ✓ | Choose as needed |
| Musculoskeletal Health | — | — | — | ✓ | Choose as needed |
| Skin Health | — | — | — | ✓ | Choose as needed |
| Respiratory Health | — | — | — | ✓ | Choose as needed |
| Growth & Bone Health | — | — | — | ✓ | Choose as needed |
| Professional Report: Healthcare Provider Summary | — | — | — | ✓ | Choose as needed |
| Professional Report: Specialist Summary | — | — | — | ✓ | Choose as needed |
| Professional Report: Genetic Counseling Summary | — | — | — | ✓ | Choose as needed |
| Immune System Health | — | — | — | — | Selectable |
| Neurological Health | — | — | — | — | Selectable |
| Nutritional & Metabolic Health | — | — | — | — | Selectable |
| Endocrine Health | — | — | — | — | Selectable |
| Ehlers-Danlos Syndrome Research | — | — | — | — | Selectable |
| Dysautonomia & Related Conditions | — | — | — | — | Selectable |
| Colorectal Cancer Risk | — | — | — | — | Selectable |
| Skin Cancer Risk | — | — | — | — | Selectable |
| Pancreatic Cancer Risk | — | — | — | — | Selectable |
| Kidney Cancer Risk | — | — | — | — | Selectable |
| Thyroid Cancer Risk | — | — | — | — | Selectable |
| Rare Endocrine Cancer Risk | — | — | — | — | Selectable |
| Radiation Sensitivity | — | — | — | — | Selectable |
| Lupus & Related Conditions | — | — | — | — | Selectable |
| Parkinson’s Disease | — | — | — | — | Selectable |
| Charcot-Marie-Tooth Disease | — | — | — | — | Selectable |
| Mitchell Syndrome | — | — | — | — | Selectable |
| Marfan Syndrome | — | — | — | — | Selectable |
| Preconception & Pregnancy Planning | — | — | — | — | Selectable |
| Pediatric Health | — | — | — | — | Selectable |
| Oral Health | — | — | — | — | Selectable |
| Vision Health | — | — | — | — | Selectable |
| Hearing & Auditory Genetics | — | — | — | — | Selectable |
| Professional Report: Naturopathic Summary | — | — | — | — | Selectable |
| Professional Report: Pharmacist Summary | — | — | — | — | Selectable |
| Professional Report: Surgical Summary | — | — | — | — | Selectable |
| Genome Data Summary | — | — | — | — | Selectable |
Confirm availability and pricing for selectable items before ordering. Final report scope and turnaround are shown at checkout.
HOW IT WORKS
Sequence once. Keep using the same genome data.
- 01Collect at HomeUse the kit to collect a cheek swab sample.
- 02Quality-Controlled SequencingThe lab performs 30× target-coverage whole genome sequencing.
- 03Reports & Standard FilesView your selected reports and retain your data in your account.
- 04Choose More AppsChoose additional apps in the App Store. After payment, start new analyses using your existing genome data.
Kepler vs. Other DNA Tests
Swipe horizontally on mobile to see all brands.
| Feature | Kepler | 23andMe | AncestryDNA | FamilyTreeDNA | Dante Labs | MyHeritage DNA |
|---|---|---|---|---|---|---|
| Overview | ||||||
| Amount of genome tested | ≈100% | <0.1% | <0.1% | <0.1% | ≈100% | ≈100% |
| Sequencing depth | 30× WGS | Not WGS | Not WGS | Not WGS | 30× WGS | 2× WGS |
| Trustpilot rating | Unknown | Unknown | Unknown | Unknown | Unknown | Unknown |
| HIPAA compliance | Unknown | Unknown | Unknown | Unknown | Unknown | Unknown |
| DNA data download | ✓ | ✓ | ✓ | ✓ | × | ✓ |
| DNA data upload | ✓ | × | × | ✓ | × | × |
| Information provided | ||||||
| Ancestry / genealogy | ✓ | ✓ | ✓ | ✓ | × | × |
| Health reports | ✓ | (few) | (few) | (few) | ✓ | × |
| Wellness | ✓ | (few) | (few) | × | × | × |
| Nutrition | ✓ | ✓ | × | × | × | × |
| Fitness | ✓ | ✓ | × | × | × | × |
| Genetic counseling | ✓ | ✓ | × | × | × | × |
| Variant information | ||||||
| Single nucleotide variants (SNVs) | ✓ | (Partial) | (Partial) | (Partial) | ✓ | (Partial) |
| Insertions and deletions (INDELs) | ✓ | (few) | (few) | (few) | ✓ | (few) |
| Copy number variants (CNVs) | ✓ | × | × | × | ✓ | × |
| Structural variants (SVs) | ✓ | × | × | × | ✓ | × |
| Mitochondrial heteroplasmy | ✓ | × | × | × | × | × |
| Reference genome alignment | GRCh38 (most up-to-date) | GRCh37 | GRCh37 | GRCh37 | GRCh37 | GRCh37 |
Green ✓: available. Red ×: not available. Orange ✓: limited or partial coverage. Report scope depends on the selected bundle. Unknown: not confirmed. Data upload and download fees follow your order terms.
Ready for the next step?
Continue to GeneHub or contact the Kepler team.