Next Generation Sequencing Market Growth, Drivers, and Forecast | 2034

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The global next-generation sequencing (NGS) market is experiencing transformative growth due to the increasing demand for precision medicine, targeted therapies, and advanced genomic research.

Next Generation Sequencing Market Overview

The global next generation sequencing (NGS) market is experiencing transformative growth due to the increasing demand for precision medicine, targeted therapies, and advanced genomic research. NGS has revolutionized the field of genomics by allowing rapid sequencing of DNA and RNA at reduced costs and increased accuracy. This cutting-edge technology is widely used across research, clinical diagnostics, agriculture, and drug development. With its capability to decode genetic material in a cost-effective and scalable manner, NGS continues to disrupt traditional sequencing methods, enhancing disease detection and treatment personalization.

Next Generation Sequencing Market Size and Share

Gain in-depth knowledge of the Next Generation Sequencing Market from Expert Market Research. In 2024, the global next-generation sequencing market reached a valuation of USD 14.66 billion. With a compound annual growth rate (CAGR) of 13.30%, the market is projected to grow significantly and attain a value of USD 51.10 billion by 2034. The growth is primarily driven by increased adoption in clinical diagnostics and cancer genomics, the emergence of innovative sequencing platforms, and the ongoing expansion of genomic databases. Furthermore, government investments and private sector funding are supporting the widespread adoption of NGS technologies globally.

Next Generation Sequencing Market Trends

The shift towards personalized medicine is one of the most defining trends in the NGS market. As healthcare becomes increasingly patient-specific, NGS is instrumental in identifying unique genetic variations that influence drug response and disease susceptibility. Pharmaceutical companies are integrating NGS into drug discovery pipelines to develop targeted therapies, reducing side effects and improving treatment outcomes. The trend is expected to grow stronger with ongoing research in oncology and rare diseases.

Integration of artificial intelligence (AI) and machine learning (ML) with NGS data analysis is revolutionizing genomics interpretation. AI-driven platforms can rapidly process large genomic datasets, improving the speed and accuracy of diagnostics. This trend is helping healthcare providers make data-backed decisions in clinical settings, especially in cancer genomics and infectious disease diagnostics. AI integration is also improving the utility of NGS in population-scale genomic studies.

Adoption of NGS in non-human applications such as agriculture, food safety, and animal research is rising. In agriculture, NGS is used to improve crop yield and pest resistance by identifying favorable genetic traits. In animal research, it aids in understanding hereditary traits and breeding optimization. The use of NGS in microbiome studies is also gaining momentum, especially in the development of probiotics and soil health research.

The development of portable and real-time sequencing platforms is gaining popularity. Technologies like Oxford Nanopore’s portable sequencers enable real-time DNA/RNA sequencing even in remote or field environments. This innovation is transforming applications in outbreak surveillance, biodiversity studies, and forensic science. The trend toward miniaturized, user-friendly devices is expected to bring NGS closer to point-of-care applications in the future.

Next Generation Sequencing Market Analysis

The increasing burden of chronic and genetic diseases is driving the demand for efficient genomic diagnostics powered by NGS. Diseases like cancer, cystic fibrosis, and Alzheimer’s are being studied at the molecular level to personalize treatment using NGS-based insights.

Declining sequencing costs have democratized access to genomic technologies. Sequencing a whole genome today is significantly cheaper than a decade ago, opening new markets in low- and middle-income countries.

Government initiatives and research funding continue to stimulate market growth. Projects like the 100,000 Genomes Project in the UK and All of Us Research Program in the U.S. exemplify national efforts to integrate NGS into healthcare systems.

Rising investments in biotechnology startups and collaborations between research institutes and diagnostic firms are accelerating product development, particularly in developing multi-omics platforms integrating genomics, proteomics, and metabolomics.

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Scope of the Report
This comprehensive report offers detailed insights into the historical and forecasted trends of the global next generation sequencing market. It explores industry drivers and constraints, segmented analysis by offerings, technology, application, end-user, and region, providing actionable data to stakeholders.

Historical and Forecast Trends, Industry Drivers and Constraints, Historical and Forecast Market Analysis by Segment:

Breakup by Offerings

  • Products: Includes sequencing platforms, reagents, and consumables that form the backbone of NGS operations.
  • Services: Comprises data analysis, library preparation, and contract sequencing services that support non-core genomic facilities.

Breakup by Technology

  • Sequencing by Synthesis (SBS): Most widely adopted due to high accuracy and scalability, commonly used by Illumina platforms.
  • Ion Semiconductor Sequencing: Cost-effective and suitable for small genome and amplicon sequencing, adopted in clinical settings.
  • SMRT Sequencing: Single Molecule Real-Time sequencing by PacBio enables longer reads, ideal for complex genome analysis.
  • Nanopore Sequencing: Offers portable real-time sequencing capabilities and has expanded into field diagnostics and environmental monitoring.
  • Others: Includes pyrosequencing and other niche technologies with limited but specific applications.

Breakup by Application

  • Diagnostics: NGS enables early disease detection, especially for oncology, rare diseases, and prenatal testing.
  • Drug Discovery & Development: Used to identify genetic targets and evaluate drug efficacy through genomic markers.
  • Agriculture & Animal Research: Applied in crop improvement, livestock breeding, and disease resistance research.
  • Others: Encompasses environmental monitoring, forensic applications, and evolutionary biology research.

Breakup by End User

  • Academic & Research Institutes: Major users for fundamental research and genomic projects.
  • Pharmaceutical & Biotechnology Companies: Utilize NGS for biomarker discovery and drug pipeline development.
  • Clinical & Diagnostic Laboratories: Growing adoption for genetic screening and personalized diagnostics.
  • Others: Includes contract research organizations (CROs) and government labs.

Next Generation Sequencing Regional Insights

North America dominates the NGS market due to high investment in genomics research, favorable reimbursement policies, and presence of major players like Illumina and Thermo Fisher Scientific. The U.S. leads in adopting NGS in oncology diagnostics and clinical genomics, supported by initiatives like the NIH’s All of Us program. Canada is also investing in genome sequencing to improve indigenous and public health.

Asia Pacific is expected to witness the fastest growth during the forecast period due to growing investments in healthcare infrastructure, expanding biotech startups, and increasing public awareness. Countries like China, India, and Japan are advancing rapidly in precision medicine and genomic sequencing, supported by national health initiatives and partnerships with global genomics firms.

Market Growth
The growth of the global NGS market is fueled by the surging demand for personalized medicine, rising awareness of early disease detection, and breakthroughs in sequencing technologies. Increased use of genomics in population health management and government funding in genetic research are expected to unlock significant opportunities. Emerging markets present untapped potential for service providers and product manufacturers. Moreover, the integration of cloud computing and AI in bioinformatics will continue to streamline NGS workflows, driving further adoption.

Recent Developments & Challenges

  • In April 2025, Illumina launched a new ultra-high-throughput sequencer capable of reducing genome sequencing costs by 30%.
  • Oxford Nanopore Technologies announced a collaboration with the WHO to deploy portable sequencers in disease surveillance in Africa.
  • The U.S. FDA issued updated guidelines for clinical validation of NGS-based diagnostic tests in January 2025, enhancing regulatory clarity.
  • QIAGEN launched a new bioinformatics suite integrated with AI capabilities for real-time sequencing data analysis.

Despite these advancements, challenges persist including data privacy concerns, lack of skilled professionals, and complex regulatory landscapes. Ensuring equitable access and interoperability across different platforms remains a key hurdle.

Next Generation Sequencing Key Players

Illumina
Illumina is a global leader in NGS technology, renowned for its Sequencing by Synthesis (SBS) platforms such as NovaSeq and MiSeq. The company dominates the market due to its robust pipeline, continuous innovation, and strategic collaborations with pharma companies. Illumina’s cloud-based analytics and diagnostic solutions make it a preferred choice across research and clinical domains.

F. Hoffman-La Roche Ltd.
Roche has strengthened its position in the NGS market through its subsidiary, Roche Sequencing Solutions. The company offers comprehensive solutions combining sequencing instruments and diagnostics. Roche's focus on oncology and infectious disease diagnostics through NGS has accelerated its adoption in hospital laboratories and research centers globally.

QIAGEN
QIAGEN provides integrated NGS workflows, from sample preparation to data interpretation. It is known for its bioinformatics platforms such as CLC Genomics Workbench and Ingenuity Pathway Analysis. QIAGEN also supports low-throughput labs with cost-efficient benchtop sequencers, making it accessible for a broad user base in clinical and academic settings.

Thermo Fisher Scientific, Inc.
Thermo Fisher offers a comprehensive NGS portfolio, including Ion Torrent sequencers and AmpliSeq targeted panels. Its seamless integration of instruments, reagents, and analysis tools provides end-to-end solutions for diagnostics and research. Thermo Fisher is a key player in companion diagnostics and has numerous collaborations with pharma firms for precision oncology applications.

Other notable players in the market include Bio-Rad Laboratories, Oxford Nanopore Technologies, PierianDx, Eurofins Genomics, DNASTAR, Inc., and PerkinElmer, Inc., all contributing to the innovation and expansion of the NGS landscape.

FAQs

Q1. What is next generation sequencing (NGS)?
NGS is a modern DNA sequencing technology that allows rapid sequencing of entire genomes or specific regions with high accuracy, replacing traditional Sanger sequencing methods.

Q2. What factors are driving the growth of the NGS market?
Key drivers include the rise of personalized medicine, decreasing sequencing costs, growing use in diagnostics, government genomics initiatives, and technological advancements in sequencing platforms.

Q3. Which region holds the largest market share in the NGS industry?
North America currently holds the largest market share due to robust research infrastructure, funding, and early adoption of clinical genomics.

Q4. What are the main applications of NGS?
NGS is applied in diagnostics (especially cancer and rare disease detection), drug development, agricultural research, and personalized treatment planning.

Q5. What are the challenges faced by the NGS market?
Challenges include high initial setup costs, data interpretation complexity, regulatory hurdles, and limited access in underdeveloped regions.

Q6. What is the future outlook of the NGS market?
The market is set for robust growth, driven by expanded clinical applications, AI integration in genomics, and global initiatives for population-scale genome sequencing.

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