Next-Generation Sequencing Informatics Market Size and Share
Next-Generation Sequencing Informatics Market Analysis by Mordor Intelligence
The next-generation sequencing informatics market size touched USD 2.64 billion in 2025 and, on the strength of a 13.84% CAGR, is forecast to reach USD 5.05 billion by 2030. Rapid declines in sequencing costs, now in the USD 100-per-sample range, are expanding the volume of genomic data that must be interpreted, which in turn is stimulating fresh demand for scalable analytics solutions across the next-generation sequencing informatics market. Cloud and hybrid compute models already handle more than 480 petabases of raw output each year, a volume equivalent to 5 million whole genomes. Artificial-intelligence pipelines embedded in software such as Illumina DRAGEN and NVIDIA Clara are shortening analysis run-times by double-digit percentages while improving variant-calling accuracy, a combination that is accelerating clinical adoption in oncology, rare-disease diagnostics and population health programs. Greater regulatory clarity—illustrated by the FDA’s March 2025 guidance on AI/ML-enabled medical devices—reduces commercialization risk and is expected to speed the entry of new tools into the next-generation sequencing informatics market[1]U.S. Food and Drug Administration, “Marketing Submission Recommendations for AI/ML-Enabled Devices,” fda.gov.
Key Report Takeaways
- By offering, software led with 58.12% of next-generation sequencing informatics market share in 2024, while platforms posted the fastest 15.81% CAGR through 2030.
- By deployment mode, cloud solutions controlled 64.21% of the next-generation sequencing informatics market in 2024; hybrid architectures are rising at a 15.41% CAGR to 2030.
- By application, drug discovery accounted for 31.41% of overall revenue in 2024; precision medicine is advancing at a 16.41% CAGR through 2030.
- By end user, academic and research institutes captured 38.71% share of the next-generation sequencing informatics market size in 2024, whereas CROs and diagnostics labs are expanding at a 15.71% CAGR.
- By geography, North America dominated with 42.12% revenue share in 2024, while Asia Pacific is projected to log a 14.51% CAGR between 2025 and 2030.
Global Next-Generation Sequencing Informatics Market Trends and Insights
Driver Impact Analysis
| Driver | % Impact on CAGR Forecast | Geographic Relevance | Impact Timeline |
|---|---|---|---|
| Widening Clinical & Research Use-Cases of Genomics | +3.2% | Global, with concentration in North America & Europe | Medium term (2-4 years) |
| Sustained Decline in Sequencing Cost per Genome | +2.8% | Global | Short term (≤ 2 years) |
| Mainstream Adoption of Cloud & Hybrid Compute Architectures | +2.4% | Global, with early adoption in North America | Short term (≤ 2 years) |
| Convergence of AI/ML with Genomic Data Pipelines | +2.1% | North America, Europe, advanced APAC markets | Medium term (2-4 years) |
| Regulatory Recognition of Genomic Software as Medical Device (SaMD) | +1.7% | North America, Europe | Medium term (2-4 years) |
| Integration of Genomic Insights into EHR & Precision-Medicine Workflows | +1.5% | North America, Europe, advanced APAC markets | Long term (≥ 4 years) |
| Source: Mordor Intelligence | |||
Widening Clinical & Research Use-Cases of Genomics
Oncology programs now rely on comprehensive panels that match patients to targeted therapies, a shift that is propelling precision-medicine revenues at a 16.4% CAGR through 2030. In Frederick Health, embedding GenomOncology’s platform inside Expanse Genomics triggered therapy adjustments for 96 patients and multiplied clinical-trial referrals by 28-fold within six months[2]MEDITECH, “Expanse Genomics Case Study,” ehr.meditech.com. Rare-disease diagnostics are benefiting from long-read sequencing, and Azenta’s clinically validated test is uncovering structural variants most short-read workflows miss. Academic consortia are also scaling: the Alliance for Genomic Discovery has completed 250,000 whole genomes, enlarging training sets for drug-target identification. As these programs expand, hospitals and biopharma alike demand informatics platforms that translate complex datasets into bedside decisions, reinforcing recurrent-revenue models across the next-generation sequencing informatics market.
Sustained Decline in Sequencing Cost per Genome
Platforms from Ultima Genomics and Roche SBX are pushing per-sample costs toward USD 100 and raising throughput to seven 30× genomes per hour, respectively. Lower entry costs have unlocked population-scale projects, leading Singapore’s national precision-medicine roadmap and India’s GenomeIndia effort to commission tens of thousands of new genomes. Illumina MiSeq i100 systems, tailored for laboratories that lack cold-chain logistics, are widening uptake in emerging economies. As sequencing capital intensity wanes, data-analysis capacity rather than read generation is becoming the primary bottleneck, shifting budget allocations toward software subscriptions and managed services inside the next-generation sequencing informatics market.
Mainstream Adoption of Cloud & Hybrid Compute Architectures
NIH’s All of Us program processes up to 9,000 whole genomes a month on its Celeste serverless stack, executing 200 million serverless functions in a single year and demonstrating the scale advantages of cloud pipelines. Commercial users follow suit: more than half of the Fortune 500 life-science companies now maintain multi-cloud genomics environments to balance cost, burst capacity and sovereignty rules. Hybrid models are gaining favor in Europe and the United States after the U.S. Department of Justice’s April 2025 rule tightened outbound genomic-data transfers, prompting firms to keep raw read files in-country while outsourcing compute-intensive secondary analysis to regional zones. These architectures continue to expand the addressable customer base for the next-generation sequencing informatics market by lowering infrastructure barriers.
Convergence of AI/ML with Genomic Data Pipelines
Illumina’s DRAGEN variants engine and NVIDIA’s Parabricks toolkit together cut variant-calling run-times from hours to minutes while boosting F-scores in challenging regions by up to five percentage points. Academic initiatives such as the ML-GAP pipeline employ autoencoders and data augmentation to flag differentially expressed genes with higher recall than traditional statistics. Start-ups are layering interpretable AI on top of tertiary analysis; IntelliGenes’ I-Gene score ranks biomarker importance and guides clinicians on therapy selection. As these tools move into regulated settings, adaptive-learning logic governed by the FDA’s Total-Product-Lifecycle framework broadens clinical acceptance of AI-rich software, nudging institutions toward premium subscriptions within the next-generation sequencing informatics market.
Restraints Impact Analysis
| Restraints Impact Analysis | (~) % Impact on CAGR Forecast | Geographic Relevance | Impact Timeline |
|---|---|---|---|
| Fragmented Global Data-Privacy & Sovereignty Regulations | -2.3% | Global, with particular impact in cross-border data flows | Short term (≤ 2 years) |
| Shortage of Clinically-Trained Bioinformaticians & Validation Experts | -1.9% | Global, with acute impact in emerging markets | Medium term (2-4 years) |
| Escalating Long-Term Storage & Compute Costs for Genomic Datasets | -1.6% | Global | Long term (≥ 4 years) |
| Lack of Interoperability Among Legacy LIMS/EHR & Modern Pipelines | -1.4% | Global, with higher impact in established healthcare markets | Medium term (2-4 years) |
| Source: Mordor Intelligence | |||
Fragmented Global Data-Privacy & Sovereignty Regulations
The U.S. Department of Justice now restricts bulk genomic exports to designated “countries of concern,” compelling enterprises to install technical safeguards and submit annual audits starting October 2025. Europe’s GDPR already mandates explicit consent for secondary use, and several APAC nations have introduced data-localization clauses that complicate multi-center studies. Providers must therefore build region-segregated clouds or pursue federated-learning models, steps that inflate compliance overheads by double digits and may slow deployment cycles inside the next-generation sequencing informatics market.
Shortage of Clinically-Trained Bioinformaticians & Validation Experts
Workforce gaps persist despite new curricula from bodies such as the Institute for Genomics Education, which flag inadequate genetic-counseling capacity as a primary barrier to precision-medicine roll-outs. Clinical and Laboratory Standards Institute worksheets offer harmonized validation protocols but cannot replace hands-on expertise, especially in low-resource regions where graduate programs remain sparse[3]Clinical and Laboratory Standards Institute, “NGS Validation Worksheets,” clsi.org. The scarcity lengthens turnaround times, raises labor costs and limits the geographic diffusion of advanced analytics platforms, tempering short-term adoption rates for the next-generation sequencing informatics market.
Segment Analysis
By Offering: Software Holds the Lion’s Share, Platforms Scale Up
NGS informatics software maintained 58.12% of next-generation sequencing informatics market share in 2024 and anchors most primary and tertiary workflows, with Illumina DRAGEN and Emedgene Explainable AI driving incremental accuracy gains. Custom plug-in ecosystems, semantic-search modules and AI-assisted curation engines transform static variant files into interactive clinical reports within minutes. Cloud-native platforms, though smaller today, are expanding at a 15.8% CAGR, bundling workflow management, compliance dashboards and pay-as-you-go compute into unified workspaces that appeal to laboratories with limited in-house bioinformatics staff.
Service providers—ranging from managed-analysis shops to bespoke pipeline developers—remain indispensable for organizations lacking internal specialists. The Clinical and Laboratory Standards Institute’s structured worksheets now guide validation, yet many hospital labs still outsource tertiary-interpretation tasks. As platforms integrate drag-and-drop interfaces and container orchestration, they further erode traditional silos and enlarge the total addressable segment of the next-generation sequencing informatics market.
Note: Segment shares of all individual segments available upon report purchase
By Deployment Mode: Cloud Commands, Hybrid Flourishes
Cloud installations accounted for 64.21% of the next-generation sequencing informatics market in 2024, fueled by the need to spin up tens of thousands of CPU-hours without capital expenditure. Providers such as Google Cloud offer turnkey genomics workbenches with petabyte-scale object stores and integrated AI model hubs that reduce the mean time-to-answer for multi-omics queries.
On-premise clusters persist where data cannot leave firewalls, but steady equipment depreciation and rising energy costs are prompting a migration to hybrid set-ups. The hybrid model combines in-house secure storage for raw reads with cloud-based secondary analysis, allowing compliance with emerging sovereignty statutes while maintaining elasticity. These configurations are expected to post a 15.41% CAGR to 2030, expanding the footprint of the next-generation sequencing informatics market size for deployment solutions worldwide.
By Application: Drug Discovery Leads, Precision Medicine Accelerates
Drug discovery represented 31.41% of 2024 revenue as pharmaceutical pipelines increasingly filter candidate lists through genome-wide association data, raising Phase II success odds by a factor of 2.6. Consortia such as the Alliance for Genomic Discovery amplify this trend with population datasets that feed target-validation algorithms.
Precision-medicine modules, bolstered by decision-support plug-ins inside electronic health-record systems, are tracking a 16.41% CAGR through 2030, the fastest within applications. Consumer genomics, forensic genetics and food-safety surveillance collectively broaden the downstream customer base. Each incrementally widens the value pool of the next-generation sequencing informatics industry, sustaining diversified revenue streams beyond core pharmaceutical demand.
Note: Segment shares of all individual segments available upon report purchase
By End User: Academia Dominates, Outsourcing Ramps Up
Academic and research institutes controlled 38.71% of next-generation sequencing informatics market share in 2024 as grant-funded centers continued to pioneer algorithmic innovation and open-data repositories. These institutions often act as bellwethers, validating novel workflows before clinical hand-off.
Contract research organizations and specialized diagnostics laboratories are the fastest-growing cluster, expanding at a 15.71% CAGR. Azenta Life Sciences projects genomic-services revenue of up to USD 570 million by FY2024 on the back of outsourcing momentum. Hospitals are not far behind; platforms like MEDITECH Expanse enable bedside ordering and pharmacogenomic decision support, embedding informatics directly into care pathways and reinforcing the end-user diversification of the next-generation sequencing informatics market.
Geography Analysis
North America retained 42.12% of 2024 turnover, underpinned by deep research budgets, mature payer frameworks and an FDA stance that encourages adaptive AI in clinical genomics. Technology alliances are flourishing: NVIDIA, IQVIA and Mayo Clinic jointly train foundation models that crunch petabytes of multimodal patient data to accelerate trial matching. Tempus, meanwhile, became the first laboratory to feed structured somatic-variant results directly into Epic’s Genomics module across more than 3,000 institutions, cementing clinical workflows that lean heavily on domestic analytics vendors.
Asia Pacific is projected to compound at 14.51% a year to 2030, propelled by Singapore’s 10-year precision-medicine roadmap, Australia’s PrOSPeCT cancer program and South Korea’s K-MASTER initiative, each sequencing tens of thousands of genomes. India’s contract-research sector, growing at 10.75%, complements device uptake; Illumina’s MiSeq i100 aims squarely at labs lacking cold-chain shipping, enabling localized workflows in tier-2 cities. These moves collectively enlarge the region’s slice of the next-generation sequencing informatics market size and lay a foundation for cloud-native collaborations that respect sovereign data laws.
Europe retains a solid foothold on the back of Horizon funding and a new European Commission regulation that obliges public-health labs to adopt whole-genome sequencing for pathogen surveillance starting 2025. Partnerships like Illumina-Sequentia Biotech showcase translational uptake in food safety. Middle East & Africa and South America remain nascent but promising; initiatives such as the Quad Cancer Moonshot inject genomic infrastructure and establish early footholds for vendors courting frontier-market growth across the next-generation sequencing informatics market.
Competitive Landscape
The competitive dynamic is moderately concentrated: the top five suppliers—Illumina, Thermo Fisher Scientific, QIAGEN, Roche and DNAnexus—collectively account for an estimated 63% of global revenue, a level that translates into strong but not monopolistic pricing power. Illumina widened its portfolio by acquiring Fluent BioSciences in July 2024, adding scalable single-cell analysis that complements its sequencing and DRAGEN stacks. Roche’s Sequencing by Expansion technology promises seven 30× genomes per hour and enters pilot sites ahead of a 2026 commercial roll-out.
AI partnerships represent the newest battleground. NVIDIA is embedding GPU-accelerated pipelines inside Illumina’s multi-omics software while simultaneously collaborating with IQVIA to shorten trial start-up times. DNAnexus deepened integration with Veeva Vault RIM, allowing customers to route genomic evidence directly into regulatory submissions, and earned Frost & Sullivan accolades for its unified clinical and omics-data fabric. Analysts expect merger interest to rise further in 2025; KPMG finds that 76% of life-science executives anticipate stepping up dealmaking to plug technology gaps, a trend likely to recalibrate share positions within the next-generation sequencing informatics market.
White-space opportunities revolve around privacy-preserving analytics, particularly federated-learning frameworks that keep data resident while sharing model weights, an approach that could satisfy sovereignty statutes and open doors in tightly regulated jurisdictions. Providers moving first into this niche may carve defensible differentiation as compliance burdens mount.
Next-Generation Sequencing Informatics Industry Leaders
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Illumina Inc.
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Thermo Fisher Scientific Inc.
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QIAGEN N.V.
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F. Hoffmann-La Roche Ltd.
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Agilent Technologies Inc.
- *Disclaimer: Major Players sorted in no particular order
Recent Industry Developments
- May 2025: Illumina and Nashville Biosciences completed 250,000 whole genomes for the Alliance for Genomic Discovery, laying the groundwork for multi-omic expansion.
- February 2025: MEDITECH Expanse Genomics linked with GenomOncology at Frederick Health, changing therapy plans for 96 patients and raising trial referrals to 56 within six months.
- February 2025: Roche unveiled Sequencing by Expansion (SBX), sequencing seven genomes per hour at 30× with 99.8% accuracy; full launch slated for 2026.
- January 2025: NVIDIA partnered with IQVIA, Illumina and Mayo Clinic to embed accelerated computing into genomic pipelines and drug discovery.
- January 2025: Illumina generated 480 petabases of data in 2024 and targets high single-digit growth by 2027 through partnerships and M&A.
Global Next-Generation Sequencing Informatics Market Report Scope
As per the scope of this report, NGS is a technology in which millions of DNA strands can be sequenced through massive parallelization. This technique is also known as high-throughput sequencing. The low cost, high accuracy and speed, and precise results even from low sample inputs are the main advantages NGS offers over Sanger's sequencing method. Products and Services (NGS Informatics Services), Application (Drug Discovery, Genetic Screening, Precision Medicine, and Other Applications), End User (Hospitals and Clinics, Academic and Research Institutes, Pharmaceutical Companies, and Other End Users), and Geography (North America, Europe, Asia-Pacific, Middle East and Africa, and South America) are the segments of the Next-generation Sequencing Informatics Market. The market report also covers the estimated market sizes and trends for 17 different countries across major regions globally. The report offers the value (in USD million) for the above segments.
| NGS Informatics Software | Primary Data Analysis Tools |
| Secondary Analysis (Alignment, Assembly, Variant Calling) | |
| Tertiary Analysis & Interpretation | |
| NGS Informatics Services | Managed & Hosted Services |
| Custom Bioinformatics & Pipeline Development | |
| Training & Support Services | |
| NGS Informatics Platforms |
| Cloud-based |
| On-premise |
| Hybrid |
| Drug Discovery |
| Genetic Screening |
| Precision Medicine |
| Other Applications |
| Hospitals and Clinics |
| Academics and Research Institutes |
| Pharmaceuticals Companies |
| Other End Users |
| North America | United States |
| Canada | |
| Mexico | |
| Europe | Germany |
| United Kingdom | |
| France | |
| Italy | |
| Spain | |
| Rest of Europe | |
| Asia-Pacific | China |
| Japan | |
| India | |
| Australia | |
| South Korea | |
| Rest of Asia-Pacific | |
| Middle East & Africa | GCC |
| South Africa | |
| Rest of Middle East & Africa | |
| South America | Brazil |
| Argentina | |
| Rest of South America |
| By Offering | NGS Informatics Software | Primary Data Analysis Tools |
| Secondary Analysis (Alignment, Assembly, Variant Calling) | ||
| Tertiary Analysis & Interpretation | ||
| NGS Informatics Services | Managed & Hosted Services | |
| Custom Bioinformatics & Pipeline Development | ||
| Training & Support Services | ||
| NGS Informatics Platforms | ||
| By Deployment Mode | Cloud-based | |
| On-premise | ||
| Hybrid | ||
| By Application | Drug Discovery | |
| Genetic Screening | ||
| Precision Medicine | ||
| Other Applications | ||
| By End User | Hospitals and Clinics | |
| Academics and Research Institutes | ||
| Pharmaceuticals Companies | ||
| Other End Users | ||
| Geography | North America | United States |
| Canada | ||
| Mexico | ||
| Europe | Germany | |
| United Kingdom | ||
| France | ||
| Italy | ||
| Spain | ||
| Rest of Europe | ||
| Asia-Pacific | China | |
| Japan | ||
| India | ||
| Australia | ||
| South Korea | ||
| Rest of Asia-Pacific | ||
| Middle East & Africa | GCC | |
| South Africa | ||
| Rest of Middle East & Africa | ||
| South America | Brazil | |
| Argentina | ||
| Rest of South America | ||
Key Questions Answered in the Report
What is the projected value of the next-generation sequencing informatics market by 2030?
The sector is forecast to reach USD 5.05 billion by 2030, expanding at a 13.84% CAGR.
Which segment currently holds the largest next-generation sequencing informatics market share?
Software accounted for 58% of revenue in 2024, making it the dominant offering category.
Why are cloud deployments growing faster than on-premise solutions?
Cloud models manage petabyte-scale datasets without capital outlay and comply with evolving AI/ML regulatory frameworks, driving a 15.4% CAGR through 2030.
How are falling sequencing costs influencing demand for informatics tools?
USD 100-genome economics shift the bottleneck from data generation to analysis, boosting subscriptions for scalable software and platforms.
Which region is expected to register the fastest growth through 2030?
Asia Pacific is projected to climb at a 14.5% CAGR, lifted by large-scale national genome programs and expanding cloud infrastructure.
What are the main challenges facing the next-generation sequencing informatics industry?
Fragmented data-sovereignty rules and a shortage of clinically trained bioinformaticians pose significant hurdles to global scalability.
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