DNA Diagnostics Market by Technology (Fluorescence In Situ Hybridization, Microarray, Polymerase Chain Reaction), Application (Genetic Testing, Infectious Disease Testing, Oncology Testing), Product Type, End User - Global Forecast 2025-2032
Description
The DNA Diagnostics Market was valued at USD 12.40 billion in 2024 and is projected to grow to USD 13.59 billion in 2025, with a CAGR of 9.53%, reaching USD 25.70 billion by 2032.
A concise introduction framing the rapid technological convergence and clinical adoption driving transformation across molecular diagnostics and DNA testing ecosystems
The molecular diagnostics and DNA testing landscape is evolving at an accelerated pace driven by continuous innovation in assay technologies, informatics, and clinical adoption pathways. Emerging sequencing modalities, increasingly automated laboratory workflows, and the growing convergence of diagnostics with therapeutic decision-making are reshaping how clinical and research organizations approach genetic information. These shifts are not limited to technology alone; they encompass regulatory frameworks, reimbursement approaches, and provider workflows that together determine how quickly new assays move from development into routine use.
Against this backdrop, stakeholders from diagnostic laboratories to academic institutes are recalibrating capabilities and investments to capture the value unlocked by more precise, faster, and cost-effective analytical approaches. As the sector matures, emphasis is shifting from isolated test offerings toward integrated diagnostic solutions that combine robust laboratory instrumentation, cloud-enabled data analysis, and streamlined services. The introduction of scalable sequencing and more sensitive molecular assays is enabling broader use cases, while the need for interpretive clarity and standardized quality measures has become a central organizing principle for market participants.
Overview of the major transformative shifts shaping laboratory architecture, informatics integration, and clinical adoption across the DNA diagnostics landscape
A series of transformative shifts is redefining priorities across the DNA diagnostics ecosystem, from how assays are developed to how results are interpreted and delivered. First, there is an unmistakable move toward high-throughput sequencing platforms and next-generation workflows that expand the range of detectable variants and reduce time-to-result. These platforms are complemented by improvements in targeted molecular techniques such as PCR and fluorescence in situ hybridization, which continue to play critical roles in rapid diagnostics and confirmatory testing. The combined effect is a multi-tiered laboratory architecture in which different technologies are selected based on clinical urgency, sample type, and the desired depth of genetic resolution.
Concurrently, informatics and cloud-enabled data analysis tools have become indispensable for handling large-scale genomic outputs. Advances in laboratory information management systems and integrated analytics support faster interpretation, enable longitudinal patient tracking, and facilitate collaborative research. This technological core is matched by growing clinical demand across oncology, infectious disease, prenatal screening, and pharmacogenomics, prompting test developers to design assays that are both clinically actionable and operationally scalable. As a result, organizations are prioritizing interoperability, regulatory compliance, and pathways to reimbursement as central components of product and service roadmaps.
Detailed examination of how 2025 tariff shifts are reshaping procurement strategies, supply chain resilience, and local manufacturing considerations for diagnostic stakeholders
Tariff changes and trade policy adjustments in 2025 are influencing procurement strategies, supply chain resilience, and cost structures for diagnostic laboratories and instrument manufacturers. Elevated duties on reagents, instruments, and sequencing consumables have introduced a reconsideration of sourcing decisions and vendor relationships, and many organizations are adopting localized procurement, multi-supplier strategies, and inventory buffering to insulate operations from volatility. These operational adjustments are paralleled by contractual renegotiations and revised capital expenditure plans as buyers seek predictable total cost of ownership amid shifting import costs.
Beyond procurement, tariffs have accelerated interest in establishing local manufacturing or assembly arrangements for high-volume consumables and in qualifying alternative suppliers to reduce single-source exposure. For assay developers and service providers, the tariff environment has underscored the importance of modular product designs and adaptable logistics planning that can absorb duty fluctuations without compromising turnaround times. Importantly, near-term decisions shaped by tariff pressures are prompting longer-term strategic conversations about regional supply chain diversity and the potential benefits of onshoring critical production capabilities in markets with sustained demand.
In-depth segmentation analysis revealing how technology, application, product type, and end-user distinctions determine adoption dynamics and commercial strategies
Insightful segmentation of the DNA diagnostics arena clarifies where technological advances and clinical needs intersect, highlighting distinct commercial and operational implications for each segment. When examined by technology, the landscape encompasses fluorescence in situ hybridization, microarray, polymerase chain reaction, and sequencing, with sequencing further divided into next generation sequencing and Sanger sequencing. This technological taxonomy reveals differing value propositions: cytogenetic and microarray approaches retain strength in structural variant detection, PCR excels in targeted rapid diagnostics, and sequencing platforms provide comprehensive molecular resolution that increasingly supports both clinical and research use cases.
By application, the field spans genetic testing, infectious disease testing, oncology testing, pharmacogenomics, and prenatal testing, with genetic testing further differentiated into carrier screening, diagnostic testing, newborn screening, and predictive testing. Each application category presents unique regulatory pathways, payer dynamics, and laboratory workflows, driving specialized product features and service models. In the product type domain, consumables, instruments, kits, and software and services form the primary categories, with software and services further parsed into cloud services, data analysis tools, and laboratory information management systems; this segmentation underscores the growing commercial importance of recurring-revenue software and interpretive services that amplify the utility of hardware and kits. Finally, end users include diagnostic laboratories, hospitals and clinics, and research institutes, each of which prioritizes different attributes such as throughput, regulatory compliance, integration capability, and cost-per-test, thereby shaping demand patterns and adoption timelines across the portfolio of technologies and offerings.
Comprehensive regional insights demonstrating how distinct regulatory, reimbursement, and infrastructure factors shape diagnostic adoption across global territories
Regional dynamics continue to exert a strong influence on technology uptake, regulatory approaches, and partnership models across the DNA diagnostics landscape, with distinct opportunities and constraints evident across major global regions. In the Americas, advanced clinical adoption is supported by robust diagnostic infrastructures, strong research ecosystems, and an active payer landscape that can enable rapid translation of novel testing modalities into routine care. This environment encourages commercial models that combine high-throughput platforms with integrated data services and patient-centric result delivery.
Europe, Middle East & Africa presents a heterogeneous regulatory and reimbursement environment that rewards evidence-driven adoption; in many countries, centralized procurement and public health programs create large-scale opportunities for newborn and population screening initiatives, while regulatory harmonization efforts influence market entry strategies. Asia-Pacific demonstrates a mix of highly developed hubs and rapidly growing markets where public health investments and private sector expansion are driving significant demand for both point-of-care assays and centralized sequencing services. Across all regions, localization of supply chains, tailored regulatory strategies, and culturally informed clinician engagement are essential for successful market penetration and sustained growth.
Key company-level insights highlighting strategic integration, specialization, and partnership models that are driving competitive advantage in diagnostics and genomics
Leading organizations across diagnostics, life sciences, and health IT are focusing on integrated offerings that combine robust instrumentation, validated assay kits, and advanced data analysis, while strategic partnerships and acquisitions are being used to accelerate time-to-market for novel solutions. Companies that prioritize end-to-end workflows-linking sample processing, high-quality reagents, automation, and interpretive software-are positioned to deliver superior operational efficiency and clinical utility. This integration reduces complexity for end users and supports recurring revenue through consumables and subscription-based analytics services.
In parallel, a cohort of specialized vendors is differentiating on niche strengths such as ultrahigh-sensitivity assays for oncology, rapid point-of-contact infectious disease tests, or scalable cloud analytics tailored for multicenter research networks. These companies often collaborate with diagnostic laboratories and academic centers to co-develop clinical evidence and validation studies that accelerate adoption. Competitive advantage increasingly depends on the ability to demonstrate clinical validity, operational reliability, and interoperability with existing laboratory ecosystems, as well as to provide robust post-sale technical and regulatory support that eases deployment in diverse clinical environments.
Actionable recommendations for technology investment, regulatory engagement, and supply chain resilience to maximize adoption and long-term clinical impact
Industry leaders should prioritize investments that align technology capabilities with tangible clinical outcomes and streamlined operational delivery. Executives can accelerate adoption by designing solutions that integrate instrumentation, consumables, and analytical software, while ensuring that user workflows are intuitive and compatible with common laboratory information systems. Emphasizing modularity in product design allows organizations to offer scalable solutions that accommodate both small laboratories and large centralized facilities, reducing barriers to entry across multiple customer segments.
Additionally, proactive engagement with regulators, payers, and clinical key opinion leaders will be essential for building the evidence base necessary to support reimbursement and guideline inclusion. Leaders should also consider diversified supply chain strategies that include qualified regional suppliers and contingency inventory planning to reduce exposure to trade disruptions. Finally, investing in data stewardship, privacy safeguards, and transparent interpretive pipelines will build clinician and patient trust, enabling wider acceptance of molecular diagnostics across routine care settings and research applications.
Transparent mixed-method research methodology combining primary interviews, literature synthesis, and cross-segmentation analysis to ensure actionable and validated insights
The research underpinning this analysis integrates a mixed-method approach designed to capture both technological nuance and practical commercial implications. Primary interviews were conducted with laboratory directors, clinical leaders, and industry executives to gather qualitative insights into adoption drivers, workflow constraints, and priority unmet needs. These primary inputs were supplemented by a systematic review of peer-reviewed literature, regulatory filings, and technical whitepapers to validate technology capabilities and clinical utility across assay types and platforms.
Analytical methods included cross-segmentation mapping to identify where technologies align with clinical applications and end-user requirements, as well as scenario analysis to evaluate how external factors such as trade policy and regulatory changes influence operational decisions. Wherever possible, findings were corroborated against real-world implementation case studies to ensure the recommendations are actionable and grounded in observable practice. The methodology emphasizes transparency in source attribution and a pragmatic orientation toward decision support for commercial and clinical stakeholders.
Conclusion synthesizing how technology integration, evidence generation, and operational excellence will determine success in the evolving diagnostics environment
As diagnostic capabilities evolve, the landscape will favor solutions that combine high analytical performance with operational simplicity, interoperability, and clear clinical value. Organizations that align product development with clinician workflows, regulatory strategy, and payer evidence requirements will be better placed to translate technological potential into improved patient outcomes. The interplay of sequencing advances, targeted molecular assays, and cloud-enabled analytics is creating new possibilities for personalized medicine, while also raising expectations for data governance and interpretive clarity.
Ultimately, success in this environment will be determined by the ability to deliver reproducible, clinically actionable results at scale, supported by strong evidence and robust operational frameworks. Stakeholders who invest in adaptable platforms, strategic partnerships, and rigorous validation will create durable competitive advantages, and those who proactively address supply chain and regulatory challenges will be best positioned to capture emergent opportunities across clinical and research settings.
Note: PDF & Excel + Online Access - 1 Year
A concise introduction framing the rapid technological convergence and clinical adoption driving transformation across molecular diagnostics and DNA testing ecosystems
The molecular diagnostics and DNA testing landscape is evolving at an accelerated pace driven by continuous innovation in assay technologies, informatics, and clinical adoption pathways. Emerging sequencing modalities, increasingly automated laboratory workflows, and the growing convergence of diagnostics with therapeutic decision-making are reshaping how clinical and research organizations approach genetic information. These shifts are not limited to technology alone; they encompass regulatory frameworks, reimbursement approaches, and provider workflows that together determine how quickly new assays move from development into routine use.
Against this backdrop, stakeholders from diagnostic laboratories to academic institutes are recalibrating capabilities and investments to capture the value unlocked by more precise, faster, and cost-effective analytical approaches. As the sector matures, emphasis is shifting from isolated test offerings toward integrated diagnostic solutions that combine robust laboratory instrumentation, cloud-enabled data analysis, and streamlined services. The introduction of scalable sequencing and more sensitive molecular assays is enabling broader use cases, while the need for interpretive clarity and standardized quality measures has become a central organizing principle for market participants.
Overview of the major transformative shifts shaping laboratory architecture, informatics integration, and clinical adoption across the DNA diagnostics landscape
A series of transformative shifts is redefining priorities across the DNA diagnostics ecosystem, from how assays are developed to how results are interpreted and delivered. First, there is an unmistakable move toward high-throughput sequencing platforms and next-generation workflows that expand the range of detectable variants and reduce time-to-result. These platforms are complemented by improvements in targeted molecular techniques such as PCR and fluorescence in situ hybridization, which continue to play critical roles in rapid diagnostics and confirmatory testing. The combined effect is a multi-tiered laboratory architecture in which different technologies are selected based on clinical urgency, sample type, and the desired depth of genetic resolution.
Concurrently, informatics and cloud-enabled data analysis tools have become indispensable for handling large-scale genomic outputs. Advances in laboratory information management systems and integrated analytics support faster interpretation, enable longitudinal patient tracking, and facilitate collaborative research. This technological core is matched by growing clinical demand across oncology, infectious disease, prenatal screening, and pharmacogenomics, prompting test developers to design assays that are both clinically actionable and operationally scalable. As a result, organizations are prioritizing interoperability, regulatory compliance, and pathways to reimbursement as central components of product and service roadmaps.
Detailed examination of how 2025 tariff shifts are reshaping procurement strategies, supply chain resilience, and local manufacturing considerations for diagnostic stakeholders
Tariff changes and trade policy adjustments in 2025 are influencing procurement strategies, supply chain resilience, and cost structures for diagnostic laboratories and instrument manufacturers. Elevated duties on reagents, instruments, and sequencing consumables have introduced a reconsideration of sourcing decisions and vendor relationships, and many organizations are adopting localized procurement, multi-supplier strategies, and inventory buffering to insulate operations from volatility. These operational adjustments are paralleled by contractual renegotiations and revised capital expenditure plans as buyers seek predictable total cost of ownership amid shifting import costs.
Beyond procurement, tariffs have accelerated interest in establishing local manufacturing or assembly arrangements for high-volume consumables and in qualifying alternative suppliers to reduce single-source exposure. For assay developers and service providers, the tariff environment has underscored the importance of modular product designs and adaptable logistics planning that can absorb duty fluctuations without compromising turnaround times. Importantly, near-term decisions shaped by tariff pressures are prompting longer-term strategic conversations about regional supply chain diversity and the potential benefits of onshoring critical production capabilities in markets with sustained demand.
In-depth segmentation analysis revealing how technology, application, product type, and end-user distinctions determine adoption dynamics and commercial strategies
Insightful segmentation of the DNA diagnostics arena clarifies where technological advances and clinical needs intersect, highlighting distinct commercial and operational implications for each segment. When examined by technology, the landscape encompasses fluorescence in situ hybridization, microarray, polymerase chain reaction, and sequencing, with sequencing further divided into next generation sequencing and Sanger sequencing. This technological taxonomy reveals differing value propositions: cytogenetic and microarray approaches retain strength in structural variant detection, PCR excels in targeted rapid diagnostics, and sequencing platforms provide comprehensive molecular resolution that increasingly supports both clinical and research use cases.
By application, the field spans genetic testing, infectious disease testing, oncology testing, pharmacogenomics, and prenatal testing, with genetic testing further differentiated into carrier screening, diagnostic testing, newborn screening, and predictive testing. Each application category presents unique regulatory pathways, payer dynamics, and laboratory workflows, driving specialized product features and service models. In the product type domain, consumables, instruments, kits, and software and services form the primary categories, with software and services further parsed into cloud services, data analysis tools, and laboratory information management systems; this segmentation underscores the growing commercial importance of recurring-revenue software and interpretive services that amplify the utility of hardware and kits. Finally, end users include diagnostic laboratories, hospitals and clinics, and research institutes, each of which prioritizes different attributes such as throughput, regulatory compliance, integration capability, and cost-per-test, thereby shaping demand patterns and adoption timelines across the portfolio of technologies and offerings.
Comprehensive regional insights demonstrating how distinct regulatory, reimbursement, and infrastructure factors shape diagnostic adoption across global territories
Regional dynamics continue to exert a strong influence on technology uptake, regulatory approaches, and partnership models across the DNA diagnostics landscape, with distinct opportunities and constraints evident across major global regions. In the Americas, advanced clinical adoption is supported by robust diagnostic infrastructures, strong research ecosystems, and an active payer landscape that can enable rapid translation of novel testing modalities into routine care. This environment encourages commercial models that combine high-throughput platforms with integrated data services and patient-centric result delivery.
Europe, Middle East & Africa presents a heterogeneous regulatory and reimbursement environment that rewards evidence-driven adoption; in many countries, centralized procurement and public health programs create large-scale opportunities for newborn and population screening initiatives, while regulatory harmonization efforts influence market entry strategies. Asia-Pacific demonstrates a mix of highly developed hubs and rapidly growing markets where public health investments and private sector expansion are driving significant demand for both point-of-care assays and centralized sequencing services. Across all regions, localization of supply chains, tailored regulatory strategies, and culturally informed clinician engagement are essential for successful market penetration and sustained growth.
Key company-level insights highlighting strategic integration, specialization, and partnership models that are driving competitive advantage in diagnostics and genomics
Leading organizations across diagnostics, life sciences, and health IT are focusing on integrated offerings that combine robust instrumentation, validated assay kits, and advanced data analysis, while strategic partnerships and acquisitions are being used to accelerate time-to-market for novel solutions. Companies that prioritize end-to-end workflows-linking sample processing, high-quality reagents, automation, and interpretive software-are positioned to deliver superior operational efficiency and clinical utility. This integration reduces complexity for end users and supports recurring revenue through consumables and subscription-based analytics services.
In parallel, a cohort of specialized vendors is differentiating on niche strengths such as ultrahigh-sensitivity assays for oncology, rapid point-of-contact infectious disease tests, or scalable cloud analytics tailored for multicenter research networks. These companies often collaborate with diagnostic laboratories and academic centers to co-develop clinical evidence and validation studies that accelerate adoption. Competitive advantage increasingly depends on the ability to demonstrate clinical validity, operational reliability, and interoperability with existing laboratory ecosystems, as well as to provide robust post-sale technical and regulatory support that eases deployment in diverse clinical environments.
Actionable recommendations for technology investment, regulatory engagement, and supply chain resilience to maximize adoption and long-term clinical impact
Industry leaders should prioritize investments that align technology capabilities with tangible clinical outcomes and streamlined operational delivery. Executives can accelerate adoption by designing solutions that integrate instrumentation, consumables, and analytical software, while ensuring that user workflows are intuitive and compatible with common laboratory information systems. Emphasizing modularity in product design allows organizations to offer scalable solutions that accommodate both small laboratories and large centralized facilities, reducing barriers to entry across multiple customer segments.
Additionally, proactive engagement with regulators, payers, and clinical key opinion leaders will be essential for building the evidence base necessary to support reimbursement and guideline inclusion. Leaders should also consider diversified supply chain strategies that include qualified regional suppliers and contingency inventory planning to reduce exposure to trade disruptions. Finally, investing in data stewardship, privacy safeguards, and transparent interpretive pipelines will build clinician and patient trust, enabling wider acceptance of molecular diagnostics across routine care settings and research applications.
Transparent mixed-method research methodology combining primary interviews, literature synthesis, and cross-segmentation analysis to ensure actionable and validated insights
The research underpinning this analysis integrates a mixed-method approach designed to capture both technological nuance and practical commercial implications. Primary interviews were conducted with laboratory directors, clinical leaders, and industry executives to gather qualitative insights into adoption drivers, workflow constraints, and priority unmet needs. These primary inputs were supplemented by a systematic review of peer-reviewed literature, regulatory filings, and technical whitepapers to validate technology capabilities and clinical utility across assay types and platforms.
Analytical methods included cross-segmentation mapping to identify where technologies align with clinical applications and end-user requirements, as well as scenario analysis to evaluate how external factors such as trade policy and regulatory changes influence operational decisions. Wherever possible, findings were corroborated against real-world implementation case studies to ensure the recommendations are actionable and grounded in observable practice. The methodology emphasizes transparency in source attribution and a pragmatic orientation toward decision support for commercial and clinical stakeholders.
Conclusion synthesizing how technology integration, evidence generation, and operational excellence will determine success in the evolving diagnostics environment
As diagnostic capabilities evolve, the landscape will favor solutions that combine high analytical performance with operational simplicity, interoperability, and clear clinical value. Organizations that align product development with clinician workflows, regulatory strategy, and payer evidence requirements will be better placed to translate technological potential into improved patient outcomes. The interplay of sequencing advances, targeted molecular assays, and cloud-enabled analytics is creating new possibilities for personalized medicine, while also raising expectations for data governance and interpretive clarity.
Ultimately, success in this environment will be determined by the ability to deliver reproducible, clinically actionable results at scale, supported by strong evidence and robust operational frameworks. Stakeholders who invest in adaptable platforms, strategic partnerships, and rigorous validation will create durable competitive advantages, and those who proactively address supply chain and regulatory challenges will be best positioned to capture emergent opportunities across clinical and research settings.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
188 Pages
- 1. Preface
- 1.1. Objectives of the Study
- 1.2. Market Segmentation & Coverage
- 1.3. Years Considered for the Study
- 1.4. Currency
- 1.5. Language
- 1.6. Stakeholders
- 2. Research Methodology
- 3. Executive Summary
- 4. Market Overview
- 5. Market Insights
- 5.1. Growing consumer demand for at-home DNA test kits with extended health insights
- 5.2. Integration of artificial intelligence algorithms in genetic variant interpretation pipelines
- 5.3. Expansion of direct-to-consumer pharmacogenomic testing offerings for personalized drug dosing
- 5.4. Emergence of CRISPR-based diagnostics for rapid pathogen detection in clinical settings
- 5.5. Rising partnerships between genomic sequencing providers and payers for scalable reimbursement models
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. DNA Diagnostics Market, by Technology
- 8.1. Fluorescence In Situ Hybridization
- 8.2. Microarray
- 8.3. Polymerase Chain Reaction
- 8.4. Sequencing
- 8.4.1. Next Generation Sequencing
- 8.4.2. Sanger Sequencing
- 9. DNA Diagnostics Market, by Application
- 9.1. Genetic Testing
- 9.1.1. Carrier Screening
- 9.1.2. Diagnostic Testing
- 9.1.3. Newborn Screening
- 9.1.4. Predictive Testing
- 9.2. Infectious Disease Testing
- 9.3. Oncology Testing
- 9.4. Pharmacogenomics
- 9.5. Prenatal Testing
- 10. DNA Diagnostics Market, by Product Type
- 10.1. Consumables
- 10.2. Instruments
- 10.3. Kits
- 10.4. Software And Services
- 10.4.1. Cloud Services
- 10.4.2. Data Analysis Tools
- 10.4.3. Laboratory Information Management Systems
- 11. DNA Diagnostics Market, by End User
- 11.1. Diagnostic Laboratories
- 11.2. Hospitals And Clinics
- 11.3. Research Institutes
- 12. DNA Diagnostics Market, by Region
- 12.1. Americas
- 12.1.1. North America
- 12.1.2. Latin America
- 12.2. Europe, Middle East & Africa
- 12.2.1. Europe
- 12.2.2. Middle East
- 12.2.3. Africa
- 12.3. Asia-Pacific
- 13. DNA Diagnostics Market, by Group
- 13.1. ASEAN
- 13.2. GCC
- 13.3. European Union
- 13.4. BRICS
- 13.5. G7
- 13.6. NATO
- 14. DNA Diagnostics Market, by Country
- 14.1. United States
- 14.2. Canada
- 14.3. Mexico
- 14.4. Brazil
- 14.5. United Kingdom
- 14.6. Germany
- 14.7. France
- 14.8. Russia
- 14.9. Italy
- 14.10. Spain
- 14.11. China
- 14.12. India
- 14.13. Japan
- 14.14. Australia
- 14.15. South Korea
- 15. Competitive Landscape
- 15.1. Market Share Analysis, 2024
- 15.2. FPNV Positioning Matrix, 2024
- 15.3. Competitive Analysis
- 15.3.1. Abbott Laboratories
- 15.3.2. Adaptive Biotechnologies
- 15.3.3. Agilent Technologies, Inc.
- 15.3.4. ARUP Laboratories
- 15.3.5. Becton, Dickinson and Company
- 15.3.6. Bio-Rad Laboratories, Inc.
- 15.3.7. BioMérieux
- 15.3.8. Danaher Corporation
- 15.3.9. DNA Diagnostic A/S
- 15.3.10. Eurofins
- 15.3.11. Exact Sciences Corporation
- 15.3.12. F. Hoffmann-La Roche Ltd.
- 15.3.13. Hologic, Inc.
- 15.3.14. Illumina, Inc.
- 15.3.15. Invitae Corporation
- 15.3.16. Laboratory Corporation of America Holdings
- 15.3.17. Luminex Corporation
- 15.3.18. Myriad Genetics
- 15.3.19. Natera, Inc.
- 15.3.20. Oxford Nanopore Technologies PLC
- 15.3.21. Promega Corporation
- 15.3.22. QIAGEN GmbH
- 15.3.23. Quest Diagnostics
- 15.3.24. Siemens Healthineers
- 15.3.25. Sysmex Corporation
- 15.3.26. Thermo Fisher Scientific Inc.
- 15.3.27. Veracyte, Inc.
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