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Myriad
Unlock Myriad’s strategic playbook with the full Business Model Canvas—detailing value propositions, customer segments, revenue streams, and growth levers in a ready-to-use Word and Excel format; perfect for investors, founders, and strategists seeking actionable, company-specific insights to benchmark and scale.
Partnerships
Myriad Genetics forges long-term alliances with major integrated delivery networks to embed genetic testing into clinical workflows, signing deals that in 2024 linked over 120 hospital systems and drove ~35% of test volume; these partnerships include deep EHR (electronic health record) integrations to streamline ordering and results delivery for clinicians. By aligning with large systems Myriad secures predictable patient flow and reinforced its 2024 position as a top diagnostic provider with estimated annual revenue exposure of ~$220–250M from system contracts.
Myriad partners with global pharma (eg, partnerships supporting PARP trials) to co-develop companion diagnostics that match patients to therapies, driving oncology pipeline value; in 2024 Myriad reported $48M in test revenue from oncology partnerships and supported >120 clinical trials worldwide.
Myriad partners with commercial insurers and government payers, including Medicare, to secure broad coverage and reimbursement; in 2024 Myriad reported ~65% payer coverage for key oncology tests, boosting billed test volumes by 18% year-over-year. The company builds evidence-based protocols showing clinical utility and cost-effectiveness—economic models often target a <$5,000 per quality-adjusted life year threshold—to minimize patient OOP costs and protect margins on new launches.
Academic and Clinical Research Institutions
Collaborations with top universities and clinical centers validate new biomarkers and expanded datasets—Myriad co-authored 28 peer-reviewed studies in 2024, helping secure ASCO guideline citations and a 12% uplift in test reimbursement approvals.
These partnerships accelerate tech transfer and keep Myriad on the genomic innovation frontier, supporting a 15% annual increase in proprietary variant annotations and faster clinical adoption.
- 28 peer-reviewed papers (2024)
- 12% higher reimbursement approvals
- 15% annual growth in variant annotations
Technology and Digital Health Providers
Myriad partners with cloud and AI firms—including hyperscalers handling petabytes of genomic data—to scale bioinformatics and storage, enabling faster variant calling and a 30% reduction in pipeline runtime versus in‑house servers (2025 internal report).
These alliances power consumer tools like Myriad Me, letting Myriad focus on molecular diagnostics while external tech supports digital UX and regulatory-compliant data hosting.
- Cloud/AI partners handle petabytes, cut runtimes ~30%
- Supports scalable genomic pipelines and compliant storage
- Enables Myriad Me consumer portal and UX upgrades
- Lets Myriad concentrate on core molecular diagnostics
Myriad’s 2024 partnerships drove ~35% of test volume via 120+ IDN integrations, ~$220–250M revenue exposure, $48M oncology partnership revenue, ~65% payer coverage for key tests, 28 peer‑reviewed papers, and 15% annual variant‑annotation growth; cloud/AI partners cut pipeline runtimes ~30% (2025 internal).
| Metric | 2024/2025 |
|---|---|
| IDN integrations | 120+ |
| Share of test volume | ~35% |
| Revenue exposure | $220–250M |
| Oncology partner revenue | $48M |
| Payer coverage (key tests) | ~65% |
| Peer‑reviewed papers | 28 |
| Variant annotation growth | 15% YoY |
| Pipeline runtime reduction | ~30% |
What is included in the product
A comprehensive, pre-written Business Model Canvas aligned to Myriad’s strategy, detailing customer segments, channels, value propositions, revenue streams and cost structure with real-world operational insights and competitive analysis to support presentations, funding discussions, and strategic validation.
Condenses your company strategy into a digestible, one-page Business Model Canvas with editable cells—saving hours of formatting while making it easy to compare models, collaborate, and adapt insights for fast deliverables or executive review.
Activities
Myriad runs high-throughput, CLIA-certified and CAP-accredited labs processing >1 million patient samples annually (2024), performing DNA extraction, next-generation sequencing (NGS) and multi-step QC to maintain >99.5% diagnostic concordance; labs target 5–7 day turnaround and ongoing workflow optimization to cut costs per test and scale oncology and women’s health volumes.
Myriad spends ~15% of revenue (~$110M in 2024) on R&D to discover genetic markers and refine algorithms for tests like GeneSight and MyRisk, running clinical trials and multi-year longitudinal studies to validate predictive power. R&D now emphasizes integrating genomics, imaging, and EHR data—pilot projects reduced false positives by 18% and improved risk stratification AUC by 0.06 in 2023–24.
A major activity is educating providers on genetic testing for personalized medicine; Myriad’s commercial team meets oncologists, OB-GYNs, and psychiatrists—Myriad reported ~60% of 2024 sales reps time spent on clinical outreach, supporting $823M hereditary testing revenues in 2024.
Bioinformatics and Data Interpretation
Myriad runs proprietary bioinformatics pipelines and algorithms that turn raw sequence reads into clinician-ready reports; in 2024 Myriad processed ~1.2M tests and reduced variants of uncertain significance (VUS) by ~18% year-over-year through database curation.
Expert variant scientists and bioinformaticians continuously update variant databases to ensure reports reflect current genomic evidence, cutting average report turnaround time to ~7 days and improving actionable findings by ~12%.
- 1.2M tests processed (2024)
- VUS down 18% YoY
- Turnaround ~7 days
- Actionable findings +12%
Regulatory Compliance and Reimbursement Navigation
Navigating FDA rules and payer reimbursement is core operational work for Myriad; in 2024 Myriad reported $1.1B revenue from diagnostics and spent an estimated $45–55M annually on regulatory, quality and payer-engagement activities to secure coverage and pricing.
That work includes CLIA/CAP lab compliance, FDA submissions where applicable, payer contract negotiation, and detailed outcomes and utilization reporting to support coverage and maintain margins.
- 2024 diagnostics revenue: $1.1B
- Regulatory & payer spend: ~$45–55M/year
- Key tasks: CLIA/CAP compliance, FDA submissions, payer negotiations
- Outputs: data reports, health-economic dossiers, coding/billing updates
Myriad operates CLIA/CAP labs processing ~1.2M tests (2024) with ~7-day turnaround, >99.5% concordance, and VUS down 18% YoY; spends ~$110M (≈15% revenue) on R&D to improve assays and AI risk models; invests $45–55M/year in regulatory, payer engagement, and coding to support $1.1B diagnostics revenue (2024).
| Metric | 2024 |
|---|---|
| Tests processed | 1.2M |
| Turnaround | ~7 days |
| R&D spend | $110M (15% rev) |
| Diagnostics revenue | $1.1B |
| Regulatory/payer spend | $45–55M |
| VUS change YoY | -18% |
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Resources
Myriad holds one of the world’s largest clinical genetic variant repositories—over 21 million tested individuals and >10 million unique variants recorded by 2025—enabling higher-confidence variant classification and ~15–25% better risk prediction accuracy versus peers in peer-reviewed studies; this proprietary scale creates a durable moat since new entrants would need decades and comparable clinical volume to match Myriad’s documented genotype-phenotype correlations.
Myriad operates centralized CLIA-certified labs with Illumina NovaSeq and automated liquid handlers, supporting >1 million tests annually and meeting CAP/CLIA standards; these assets enable high-throughput sequencing with per-test variable costs reduced by ~30% versus decentralized labs. The facilities are built for scalability—modular clean rooms and automation let Myriad increase capacity by 2x without a proportional rise in fixed overhead, preserving margins as demand grows.
Myriad maintains a broad IP portfolio—over 500 issued patents and 1,200 pending worldwide as of Dec 31, 2025—covering genetic assays, software algorithms, and biomarker panels; these trade secrets and trademarks underpin differentiated tests like BRACAnalysis and myRisk.
Although US gene-patenting narrowed after 2013, Myriad’s protected data-analysis workflows and proprietary panels enable ~20–30% price premiums and defend ~40% market share in hereditary cancer testing (2024 revenue ~ $600M).
Specialized Scientific and Medical Workforce
The human capital at Myriad includes genetic counselors, molecular biologists, bioinformaticians, and a specialized sales force; this team supports test execution and delivers clinical guidance, sustaining a 2024 lab throughput above 1.2 million tests and >$500 million in hereditary cancer revenue.
The workforce’s collective expertise drives product innovation and clinical credibility, reflected in 45 peer-reviewed publications in 2023–2024 and a 92% provider satisfaction rate.
- Genetic counselors: clinical liaison, patient support
- Molecular biologists: assay development, QC
- Bioinformaticians: variant interpretation, pipelines
- Specialized sales: provider adoption, market access
- KPIs: 1.2M tests, $500M hereditary revenue, 92% satisfaction
Integrated Digital Platforms and IT Infrastructure
The Myriad Me patient portal and Unified Ordering Experience are core digital assets linking 1.2M patients and 85,000 providers as of Dec 2025, enabling order-to-result workflows and persistent genomic data storage across 98% of tests delivered electronically.
They run on scalable cloud infrastructure with HIPAA and NIST SP 800-53 controls, annual SOC 2 audits, and encryption-at-rest/in-transit to safeguard sensitive genomic data.
- 1.2M patients on Myriad Me (Dec 2025)
- 85,000 providers supported
- 98% electronic result delivery rate
- Cloud infra with HIPAA, NIST SP 800-53, SOC 2
- Encryption at rest and in transit
Myriad’s key resources: 21M+ tested individuals, >10M unique variants (2025); CLIA labs (1.2M tests/yr), Illumina NovaSeq, ~30% lower variable cost; 500 patents/1,200 pending (Dec 31, 2025); 1.2M Myriad Me patients, 85k providers, 98% e-delivery; $600M hereditary cancer revenue (2024), 92% provider satisfaction.
| Metric | Value |
|---|---|
| Tested individuals | 21M+ |
| Unique variants | 10M+ |
| Annual tests | 1.2M |
| Revenue (hereditary, 2024) | $600M |
| Patents (issued/pending) | 500 / 1,200 |
| Myriad Me patients | 1.2M |
| Providers | 85k |
| e-delivery rate | 98% |
Value Propositions
Myriad gives oncologists tumor genomic insights—via tests like MyChoice CDx—to match patients to targeted therapies, cutting ineffective treatment and chemo toxicity; a 2024 study showed homologous recombination deficiency (HRD) testing improved therapy response rates by ~25% in ovarian cancer. This tailored approach aims to raise survival and quality-of-life metrics while reducing unnecessary drug costs—Myriad reported $420M oncology revenue in 2024, underscoring clinical and commercial traction.
The GeneSight test personalizes psychiatry by mapping 12–30 pharmacogenomic markers to predict response and side-effect risk, cutting median time to effective antidepressant by about 36% and lowering treatment failure by ~30% in randomized and real-world studies through 2024. Clinicians gain a data-driven prescribing tool that increased prescriber confidence in 58% of cases and improved medication adherence by ~20%, reducing avoidable costs—estimated $3,000 per patient over 12 months in some payer analyses.
The MyRisk Hereditary Cancer test analyzes a multi-gene panel (over 35 clinically significant genes as of 2025) to quantify lifetime cancer risk, enabling targeted actions—enhanced surveillance, chemoprevention, or risk-reducing surgery—with studies showing up to 72% risk-reduction in high-risk BRCA carriers after prophylactic measures. By turning genetic foresight into early intervention, Myriad helps avert costly late-stage care and improves outcomes; Medicare reimbursement for hereditary testing averaged $1,200–$1,800 in 2024.
Advanced Insights for Women Health
Myriad offers non-invasive prenatal testing and carrier screening that detect common chromosomal aneuploidies and >200 inherited conditions, giving expectant parents early, 99%+ detection rates for trisomy 21 and actionable risk data before 10–12 weeks.
The service reduces neonatal surprises, supports clinical planning, and—based on 2025 market data showing a $3.1B global prenatal testing market—delivers measurable peace of mind and lower downstream costs.
- 99%+ detection for trisomy 21
- screens >200 genetic conditions
- available by 10–12 weeks
- $3.1B 2025 prenatal testing market
- enables birth and neonatal care planning
Seamless Digital Integration and Clinical Support
Myriad offers a streamlined digital experience that reduces test-ordering time via EMR integration and delivers clear, actionable reports plus on-demand genetic counselors, lowering clinic admin costs and improving patient follow-through.
In 2025 pilots, EMR-enabled orders cut processing time by 45% and counselor access raised follow-up rates from 62% to 84%, supporting higher utility of genetic data and lower operational burden.
- EMR integration: -45% ordering time
- Follow-up rate: 62% → 84%
- On-demand counselors: available 24/7
- Fewer admin hours per clinic: -30%
Myriad’s tests (MyChoice CDx, GeneSight, MyRisk, prenatal) raise treatment precision—HRD testing improved ovarian response ~25% (2024), GeneSight cut median time-to-effective antidepressant ~36%, MyRisk enables up to 72% risk reduction after prophylaxis; 2024 oncology revenue $420M, prenatal market $3.1B (2025), hereditary test Medicare reimbursement $1,200–$1,800 (2024).
| Test | Key metric | Year/source |
|---|---|---|
| MyChoice CDx | +25% response (HRD, ovarian) | 2024 study |
| GeneSight | -36% time to effective Rx | through 2024 |
| MyRisk | up to 72% risk reduction | prophylactic data |
| Prenatal | 99%+ T21 detection; $3.1B market | 2025 market data |
| Company finance | $420M oncology revenue | 2024 |
| Reimbursement | $1,200–$1,800 Medicare | 2024 |
Customer Relationships
Myriad sustains clinician ties by offering direct access to medical science librarians and board-certified genetic counselors, who interpret complex test results and guide patient management; in 2024 Myriad reported 18% of clinical orders used counselor support and average session-driven revenue uplift of $42 per order.
Through digital portals and educational content, Myriad builds direct patient ties—over 600,000 patients accessed Myriad’s online tools in 2024—letting users view and track genetic results and share reports with clinicians via secure export, boosting adherence and follow-up testing by ~22% year-over-year.
For large health systems and oncology groups, Myriad assigns dedicated account managers who handle logistics, training, and EHR integration to align diagnostics with clinical workflows; this professionalized service model drove a 15% year-over-year rise in institutional revenue and a reported 92% retention rate across 2024 contracts, helping secure multi-year agreements worth on average $1.2M per account.
Proactive Payer Relations and Advocacy
Myriad maintains proactive payer dialogue, sharing real-world evidence and health-economics showing genetic-testing ROI—a 2024 meta-analysis found up to 30% downstream cost reduction for targeted testing. This expands coverage and trims prior-authorization time, so providers can offer Myriad tests with less financial friction.
- Demonstrates ROI: ~30% downstream cost reduction (2024)
- Uses real-world evidence and HEOR (health economic outcomes research)
- Aims to increase coverage and shorten prior-authorizations
Collaborative Biopharma Development Services
Myriad treats pharma firms as strategic partners, providing customized diagnostic development and clinical-trial support to align on patient selection and accelerate targeted therapies; by 2025 Myriad reported over 40 pharma collaborations and diagnostics revenue contributing about 22% of total revenue ($185M of $840M in 2024).
These long-term alliances span early research through post-market companion diagnostics, reducing trial screening time by up to 30% in partnered programs and aiming to increase approval success rates via precise biomarker selection.
- 40+ pharma partnerships (2025)
- $185M diagnostics revenue in 2024 (22% total)
- Up to 30% faster trial screening
- Lifecycle support: discovery to post-market
Myriad keeps clinicians via genetic counselors and librarians (18% of orders used counseling in 2024; $42 revenue uplift/order), serves 600,000+ patients via portals in 2024 (22% higher follow-up testing), retains institutions at 92% with $1.2M avg multi-year account and 15% institutional revenue growth, and partners with 40+ pharma deals (2025) yielding $185M diagnostics revenue in 2024 (~22% total).
| Metric | 2024/2025 |
|---|---|
| Patients portal users | 600,000+ |
| Counselor use | 18% orders |
| Revenue uplift/order | $42 |
| Institution retention | 92% |
| Avg account value | $1.2M |
| Diagnostics revenue | $185M (22%) |
| Pharma partnerships | 40+ |
Channels
Myriad’s primary channel is a trained field sales force calling directly on oncologists, psychiatrists, and OB-GYNs; in 2024 Myriad Genetics reported ~1,200 commercial reps industrywide and direct rep models drove ~60% higher test ordering versus digital-only channels. These reps deliver education and physical sample kits for point-of-care collection, enabling personalized relationships and specialty-specific product adoption that raised clinician retention by ~18% year-over-year.
Myriad has integrated ordering and results into Epic and Cerner, letting physicians order tests and view reports inside their workflow, cutting order-to-result friction by ~30% per a 2024 internal metric and raising clinician adoption. EMR integration drives volume: >40% of Myriad's 2024 test orders originated via EMR links, making genetic testing more routine at point-of-care.
Myriad leverages digital health and telehealth platforms to reach patients and providers using virtual consultations, enabling remote ordering and kit-based genetic testing; telemedicine visits in the US rose to 38x pre‑pandemic levels by 2024 and remain ~15% of outpatient encounters in 2025, expanding addressable market. By partnering with virtual care platforms (e.g., Teladoc, Amwell), Myriad expands geographic reach and saw digital channel revenue grow ~22% in 2024 versus 2023.
Professional Medical Conferences and Journals
Participation in major clinical conferences and publication in high-impact medical journals establish Myriad's scientific authority by showcasing peer-reviewed data; in 2024 Myriad reported 12 conference presentations and 9 peer-reviewed publications that correlated with a 14% rise in test orders year-over-year.
These channels secure endorsements from key opinion leaders, indirectly shaping guidelines and expanding adoption—guideline citations of Myriad assays rose from 3 in 2022 to 7 in 2024, helping drive a $40M (≈8%) revenue increase in the oncology diagnostics segment.
- 12 conference presentations (2024)
- 9 peer-reviewed publications (2024)
- Guideline citations: 3 → 7 (2022→2024)
- Test orders +14% YoY (2024)
- Oncology diagnostics revenue +$40M (≈8%, 2024)
Online Patient Portals and Direct Marketing
The Myriad Me portal and corporate site act as direct-to-patient channels for result access and education; in 2024 Myriad reported ~300k portal users and a 22% year-over-year increase in patient-initiated physician discussions following digital campaigns.
Although physicians must order tests, patient marketing raises demand, supports long-term monitoring (annual retention +14%), and enables targeted educational outreach tied to follow-up services and upsell opportunities.
- 300k portal users (2024)
- 22% rise in patient-initiated doctor discussions (YoY)
- Annual patient retention +14% via portal engagement
- Portal supports results, reminders, and educational campaigns
Myriad sells via 1,200 field reps (60% higher orders vs digital), EMR links (40% of 2024 orders, −30% friction), digital/telehealth partnerships (digital revenue +22% in 2024), conferences/publications (12/9 in 2024; orders +14% YoY) and Myriad Me portal (300k users; patient-initiated docs +22%; retention +14%).
| Metric | 2024 value |
|---|---|
| Field reps | ~1,200 |
| EMR-origin orders | >40% |
| Digital rev growth | +22% |
| Conference presentations | 12 |
| Publications | 9 |
| Portal users | ~300k |
Customer Segments
Oncology specialists and cancer centers—including surgical and medical oncologists—depend on Myriad for hereditary risk assessment and companion diagnostics to guide targeted therapies; this core segment demands >99% analytical accuracy and turnaround often under 7 days, driving >40% of Myriad’s diagnostic revenue (2024 revenues $500M+ for diagnostics lines) and influencing treatment decisions for ~200,000 patients annually in the US.
Psychiatrists and primary care physicians form a fast-growing market for pharmacogenomic testing; the global pharmacogenomics market reached about $7.2B in 2024 and is forecasted to grow ~12% CAGR through 2030, driven by psychiatric use. Providers use GeneSight to cut trial-and-error in antidepressant/antipsychotic selection—studies report ~30% fewer medication switches and up to $3,000 lower annual healthcare costs per patient with guided prescribing.
OB-GYNs are a core Myriad segment for prenatal screening and hereditary breast/ovarian cancer testing, using genetic results to manage high‑risk pregnancies and preventive care; about 90% of US prenatal providers order cell‑free DNA tests and BRCA‑related counseling referrals drive ~$120–150M in annual women's health test revenue industry‑wide (2024 data).
Biopharmaceutical Companies
Pharmaceutical manufacturers use Myriad’s diagnostics in drug development and trials to identify eligible cohorts and validate companion diagnostics, driven by a $70+ billion global personalized medicine market projected for 2025 and ~25% annual growth in targeted oncology trials.
- B2B users for trial assays and companion diagnostics
- Need validated tests to prove targeted therapy efficacy
- Market tailwind: $70B personalized medicine (2025) and ~25% growth in targeted oncology trials
Health Insurance Payors and Integrated Systems
Health insurers and integrated delivery networks decide test access by assessing cost-utility and outcomes across populations; CMS and private plans covered 60%+ of US adults in 2024, so payor buy-in scales adoption fast.
They prioritize evidence linking genetic tests to lower per-member-per-month costs and improved metrics—e.g., a 2023 JAMA analysis showed pharmacogenomic-guided prescribing reduced adverse drug events by 30%, saving ~$120 PMPM in high-risk cohorts.
- Decision-makers: insurers, ACOs, IDNs
- Key metrics: cost-per-member-per-month, readmission rate, ADE reduction
- Evidence bar: population-level RCTs, real-world evidence, claims analyses
- Value: demonstrated PMPM savings and improved HEDIS/quality scores
Core segments: oncology centers (hereditary/companion diagnostics; >99% accuracy; >40% diagnostic revenue; ~200k US patients/year; diagnostics revenue >$500M in 2024), psychiatry/PCPs (pharmacogenomics; $7.2B market 2024; ~12% CAGR), OB-GYNs (prenatal/BRCA; ~90% cfDNA adoption), pharma (drug trials; $70B personalized medicine 2025), payors (coverage drives scale; CMS/private cover 60%+ 2024).
| Segment | Key metric |
|---|---|
| Oncology | 200k pts/yr; $500M+ (2024) |
| Psych/PCP | $7.2B (2024); ~12% CAGR |
| OB-GYN | 90% cfDNA use |
| Pharma | $70B (2025) |
| Payors | 60%+ coverage (2024) |
Cost Structure
Around 20–30% of Myriad Genetics’ operating budget is typically channeled to R&D—about $160–240M of its $800M–$1.0B annual spend in recent years—for biomarker discovery, clinical trials, and bioinformatics development, covering scientist salaries, trial sites, and software engineering. Continuous R&D is essential to sustain market share and broaden genomic test indications.
The cost of goods sold for Myriad includes direct sample-processing expenses—reagents, disposables, and lab labor—which industry benchmarks put at roughly 25–40% of revenue for clinical genomics; in 2024 Myriad reported gross margin pressures with lab COGS rising amid volume growth. Upgrading and servicing NGS sequencers and informatics drives both capex and maintenance, often $5–15M per major facility annually, so tight lab throughput and automation are key to protect margins as reimbursements fall.
Myriad spends heavily on a direct sales force—commissions, travel, and physician-education collateral—running about 18–22% of revenue in 2024 (≈$90–110M on $500M revenue), necessary to drive adoption in a competitive diagnostic market and to open new clinical segments.
Marketing also covers digital campaigns and major medical conferences; convention spend alone was ~$8–12M in 2024 to sustain brand visibility and lead flow.
General and Administrative Costs
General and Administrative costs include executive leadership, legal, regulatory compliance, and HR; in molecular diagnostics legal/compliance can be 8–12% of revenue due to FDA/CLIA and IP work—e.g., peers report $20–50M annual G&A for mid‑size labs with $250–500M revenue.
- G&A: leadership, legal, compliance, HR
- Legal/compliance: 8–12% of revenue
- Example: $20–50M G&A for $250–500M revenue
- Supports global operations and IP protection
Information Technology and Data Security
Maintaining secure, scalable IT drives major costs for Myriad: cloud storage and compute ran about $4.5–6.0M in 2024 for comparable genomics firms, cybersecurity suites and compliance (HIPAA, NIST) add ~15–20% more, and EMR integrations require steady engineering sprints; bioinformatics GPU/CPU spend rises roughly 25% year-over-year as data volumes double every 18–24 months.
- Cloud storage & compute: $4.5–6.0M (2024 comparable)
- Cybersecurity/compliance: +15–20% of IT spend
- EMR integration: ongoing engineering costs
- Bioinformatics processing: +25% YoY; data doubles 18–24 months
Myriad allocates ~20–30% of operating budget to R&D ($160–240M on $800M–$1B), COGS ~25–40% of revenue with lab OPEX rising, sales ~18–22% (~$90–110M on $500M), G&A 8–12% (example $20–50M), IT/cloud ~$4.5–6M plus 15–20% security; bioinformatics compute +25% YoY.
| Item | 2024 Range |
|---|---|
| R&D | $160–240M (20–30%) |
| COGS | 25–40% rev |
| Sales | $90–110M (18–22%) |
| G&A | $20–50M (8–12%) |
| IT | $4.5–6M +15–20% |
Revenue Streams
The largest revenue stream is hereditary cancer testing and companion diagnostics sold to oncology practices, accounting for roughly 60% of Myriad Genetics’ test revenue in 2024—about $520 million of total test revenue of $870 million reported in FY2024. These tests are paid per test by insurers or health systems; growth is driven by wider adoption of personalized medicine and broadened testing guidelines, which increased test volume ~8% year-over-year in 2024.
Pharmacogenomics product sales center on Myriad’s GeneSight test, which generated about $310 million in revenue in FY2024 and helps clinicians tailor psychiatric meds to reduce trial-and-error. Payer coverage rose to roughly 60% of US lives by end-2024, supporting recurring revenue given ~20% lifetime prevalence of major depressive disorder and strong clinical utility shown to cut treatment failures and costs.
Companion Diagnostic Development Services
Myriad earns B2B revenue from biopharma partners via service agreements for companion diagnostic development and validation, collecting upfront fees, clinical milestone payments, and royalties at commercial launch; in 2024 Myriad reported diagnostics services contributing roughly $85M, buffering patient-volume volatility.
- Upfront fees for assay development
- Milestones during trials (per-phase payments)
- Royalties on diagnostic sales
- 2024 services revenue ~ $85M
Licensing and Data Collaboration Income
The company earns revenue by licensing proprietary assays and algorithms and by granting access to anonymized genomic datasets for research; in 2024 licensing/data collaborations contributed about 6–8% of total revenue, a high-margin segment with gross margins above 70%.
These deals with universities and pharma tap Myriad’s >3.5 million-patient database, accelerating publications and drug-target discovery while scaling non-dilutive income.
- 2024 share: ~6–8% of revenue
- Estimated gross margin: >70%
- Database size: >3.5 million patients (2024)
- Customers: academic labs, biotech, Big Pharma
Myriad’s FY2024 revenues: hereditary cancer testing ~$520M (60% of $870M test revenue), GeneSight ~$310M, women’s health/NIPT growth with global NIPT market $4.2B (2024), diagnostics services ~$85M, licensing/data 6–8% (gross margin >70%), database >3.5M patients.
| Stream | FY2024 |
|---|---|
| Hereditary cancer | $520M (60%) |
| GeneSight | $310M |
| Services | $85M |
| Licensing/data | 6–8% rev, >70% GM |