Jura Health
- Company typePrivate
- Founded2017
- HeadquartersDenver, United States
- Headcount1–10
- GTM typeB2B and B2C
- OfferingServices
Jura Health firmographics
Firmographics- Name
- Jura Health
- Legal name
- Jura Health US Inc.
- Website
- https://jura.health
- Company type
- Private
- Founded year
- 2017
- Operating status
- Operating
- Headcount range
- 1–10 employees
- Ownership category
- akta.pro rank
Jura Health industry classification
Industry- Product category
- Rare Disease Genetic Diagnostics
- NAICS
- Medical Laboratories (621511)
- SIC
- Services-Medical Laboratories (8071)
- akta.pro primary industry
- Genetic & Prenatal Testing Laboratories (HLAFAMAH)
- akta.pro secondary industries
- Molecular & Genetic Testing (PCR/NGS/qPCR) (HLAGADAF), Genetic & Genomic Testing (germline, somatic, carrier, pharmacogenomics) (HLAAALAD)
Keywords
Where Jura Health is headquartered
LocationHeadquarters
- HQ city
- Denver
- HQ country
- United States
- HQ region
- North America
Offices2 records
Markets served
Jura Health business model
Business model- GTM type
- B2B and B2C
- Offering type
- Services
- Cost components
- Personnel, Technology or R&D, Marketing or Sales, Operations, Infrastructure, Others
Revenue model
- Whole Genome Sequencing Testing: One-time clinical WGS test delivered through the Emerge Platform. Cash-pay available in all 50 states. Medicaid reimbursement currently approved in Colorado and Louisiana, with plans to expand to additional states.
- Standalone Genetic Counseling: A la carte genetic counseling sessions priced at $50 cash pay, including 30 minutes of live 1:1 conversation plus 30 days of asynchronous chat. Free genetic counseling is included with every Emerge test order.
- Medicaid Reimbursement: Jura Health is an approved Medicaid provider in Colorado and Louisiana for suspected rare disease testing, enabling reimbursement through state Medicaid programs.
Pricing tiers
| Model | Billing | Price |
|---|---|---|
| Subscription | Pay-as-you-go | Emerge Whole Genome Sequencing Test — Medicaid covered |
| One time/ perpetual license | Pay-as-you-go | Emerge Whole Genome Sequencing Test — Cash Pay |
| Unit Pricing | Pay-as-you-go | Standalone Genetic Counseling Session |
Go-to-market motion3 records
Distribution channels4 records
Marketing channels7 records
Jura Health product offering
Product offeringCore offering
Jura Health provides comprehensive whole genome sequencing (WGS) via its Emerge™ Platform, combining at-home saliva sample collection, clinical sequencing through Broad Clinical Labs, multilingual on-demand genetic counseling in up to 50 languages, and personalized disease-specific next-steps resources (advocacy groups, clinical trials, insurance support). Results are delivered as clinical reports to physicians within 4–5 weeks, with optional Pharmacogenomics (PGx) and Nutrigenomics (NGx) reports and a free ACMG 84 actionable gene panel included with each test.
Product overview
Jura Health offers a unified platform architecture centered on the Emerge™ Platform, which combines at-home saliva-based whole genome sequencing (via the Emerge™ DNA Test) with integrated genetic counseling and personalized follow-up resources. The core offering includes multiple report modules: Whole Genome Sequencing Report, Genetic Counselor Clinical Summary, Emerge Next Steps Resources, Pharmacogenomics Report, and Nutrigenomics Report—all delivered through Broad Clinical Labs. Add-on services include Genetic Counseling Support sessions and the opt-in ACMG 84 panel available at no extra cost. Provider-focused Payer Resources are also offered to support reimbursement workflows.
Differentiator
Problem solved
Functional benefit
Brands
- Emerge Platform: Whole genome sequencing and analysis platform with on-demand multilingual genetic counseling and disease-specific next steps support.
Products and services
- Emerge™ Platform An end-to-end health platform that combines at-home saliva sample collection, whole genome sequencing via Broad Clinical Labs, multilingual on-demand genetic counseling in 50 languages, and disease-specific next-steps resources (advocacy groups, clinical trials, insurance support) for patients and families facing rare or undiagnosed diseases.
- Emerge™ DNA Test An at-home saliva sample kit that sequences a patient's whole genome and delivers a full clinical report to the ordering physician within 4–5 weeks, designed to address the average 6-year diagnostic delay for rare diseases in children. Available cash-pay in all 50 states and reimbursed by Medicaid in Colorado and Louisiana.
- Standalone Genetic Counseling A standalone genetic counseling session priced at $50 cash pay, providing 30 minutes of live 1:1 conversation with a genetic counselor plus 30 days of asynchronous chat in 50 languages. Free genetic counseling is bundled with every Emerge DNA Test order.
Quantifiable outcome
- Reduces rare disease diagnostic timeline from 6 years to 5 weeks
- +3 more outcomes
Companies that use Jura Health
Customer profileNamed customers2 records
Segments4 records
Ideal customer profiles3 records
Jura Health technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature5 records
Jura Health partnerships and signals
Strategic signalPartnerships
Six partnerships are on record, tiered core and minor.
- Startup Prize HealthcoreLouisiana-based startup competition through which Jura Health participated and gained visibility, ultimately leading to its expansion to Louisiana. Founder Gregory Kallenberg described the expansion as evidence that the region is becoming a health innovation hub of national or international importance.
- Samba ScientificcorePartnership to improve genomic testing access to underserved populations. Samba Scientific brings complementary capabilities in scientific outreach and market access to expand Jura Health's reach in medically underserved communities.
- UGenome AIcoreCollaboration leveraging UGenome AI's genomic platform technology for rare disease patient diagnosis and personalized plans, including pharmacogenomic profiling. UGenome AI and Jura Health also partnered with Open Table to link DNA insights with community social support networks.
- Open Tablecore501(c)(3) nonprofit pioneering community-based relational and social capital solutions. Together with UGenome AI, the partnership addresses non-medical determinants of health for families facing rare disease diagnoses by linking DNA insights with community social support networks.
- Broad Clinical LabscoreCAP-accredited and CLIA-certified laboratory that powers Jura Health's whole genome sequencing. Broad Clinical Labs (BCL) powered some of the world's largest WGS projects including the Human Genome Project, providing Jura Health with validated clinical sequencing infrastructure.
- Innosphere VenturesminorColorado-based life sciences incubator that supported Jura Health through its program, culminating in graduation from Innosphere's Life Sciences Incubator. Operating under a U.S. Economic Development Administration Build to Scale Grant, the program aims to catapult participating companies' concepts into market-ready solutions.
Scale indicators5 records
Recent moves7 records
Expansion highlights6 records
Jura Health competitors and assessment
Company assessmentDirect peers
- GeneDx: GeneDx is a clinical genomics company specializing in rare disease and pediatric whole genome and exome sequencing, directly competing with Jura Health in WGS for undiagnosed children, with established payer relationships and a larger commercial footprint.
- Centogene: Centogene is a rare disease diagnostics company providing WGS, WES, and biochemical testing with multi-country rare disease registries, directly competing in the rare disease pediatric diagnostic market.
- Natera: Natera is a genetic testing company offering reproductive, oncology, and rare disease tests including whole genome and exome sequencing, overlapping directly with Jura's pediatric rare disease WGS use case.
- Invitae: Invitae (now part of Labcorp) provides comprehensive genetic testing including WGS and rare disease panels, directly competing in the same clinical genomics category as Jura Health with much broader payer coverage.
- Ambry Genetics: Ambry Genetics (a Konica Minolta company) is a clinical genetic testing lab offering exome and genome sequencing for rare and hereditary disease, a directly comparable WGS provider competing for the same pediatric rare disease market.
- BillionToOne: BillionToOne is a precision diagnostics company using NGS for reproductive health and oncology, with comparable molecular diagnostics technology and a similar focus on accessible, high-sensitivity genetic testing.
- PreventionGenetics: PreventionGenetics (now part of Exact Sciences) is a CLIA-certified clinical DNA testing laboratory offering whole genome and exome sequencing services, directly comparable in technology and clinical use case to Jura's WGS offering.
Emerging players
- 3billion: 3billion is a rare disease genetic testing company offering whole exome and genome sequencing with AI-driven interpretation, focused on shortening the rare disease diagnostic odyssey, a directly comparable value proposition to Jura Health.
Broad incumbents
- Tempus AI: Tempus is a precision medicine company using AI and genomic sequencing across oncology and rare disease, with broader portfolio offerings but overlapping WGS/NGS technology and rare disease focus.
- Myriad Genetics: Myriad Genetics is an established clinical genomics company offering hereditary cancer, pharmacogenomic, and rare disease testing, providing overlapping capabilities as a broad incumbent in the genetic testing space.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat6 records
Key risks6 records
Key highlights7 records
Customer concentration
Jura Health social profiles
Digital presenceJura Health compliance and trust
Trust signalCompliance5 records
Jura Health financial estimates
Financial estimateRevenue estimate
Valuation estimate
Jura Health leadership team
Management profileNumber of profiles
Profiles4 records
Jura Health funding detail
Funding detailFunding overview
Funding rounds1 record
Investors1 record
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Jura Health M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Jura Health
What does Jura Health do?
Jura Health provides comprehensive whole genome sequencing (WGS) via its Emerge™ Platform, combining at-home saliva sample collection, clinical sequencing through Broad Clinical Labs, multilingual on-demand genetic counseling in up to 50 languages, and personalized disease-specific next-steps resources (advocacy groups, clinical trials, insurance support). Results are delivered as clinical reports to physicians within 4–5 weeks, with optional Pharmacogenomics (PGx) and Nutrigenomics (NGx) reports and a free ACMG 84 actionable gene panel included with each test.
Is Jura Health a public or private company?
Jura Health is a private company. It is classified as venture growth investor backed and is currently operating.
When was Jura Health founded?
Jura Health was founded in 2017. It employs 1 to 10 people.
Where is Jura Health based?
Jura Health is headquartered in Denver, United States, in the North America region.
How does Jura Health make money?
Three revenue lines are on record. Whole Genome Sequencing Testing is the primary driver. The others are standalone Genetic Counseling and medicaid Reimbursement.
Who are Jura Health's main competitors?
Direct peers on record are GeneDx, Centogene, Natera, Invitae, Ambry Genetics, BillionToOne and PreventionGenetics. 3billion is listed as an emerging player. Broad incumbents are Tempus AI and Myriad Genetics.
Does Jura Health have an API?
No public API is recorded for Jura Health.
What industry is Jura Health in?
Jura Health's product category is Rare Disease Genetic Diagnostics. Its primary akta.pro industry code is HLAFAMAH, Genetic & Prenatal Testing Laboratories, with a secondary code of HLAGADAF, Molecular & Genetic Testing (PCR/NGS/qPCR). Its NAICS code is 621511 and its SIC code is 8071.