The United States next generation sequencing market size reached USD 4.4 Billion in 2024. Looking forward, IMARC Group expects the market to reach USD 20.9 Billion by 2033, exhibiting a growth rate (CAGR) of 18.9% during 2025-2033. The increasing demand for personalized medicines among the masses, the rising product adoption in agriculture and environmental research, and various advancements in automation and data analysis represent some of the key factors driving the market.
Report Attribute
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Key Statistics
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Base Year
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2024 |
Forecast Years
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2025-2033
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Historical Years
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2019-2024
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Market Size in 2024 | USD 4.4 Billion |
Market Forecast in 2033 | USD 20.9 Billion |
Market Growth Rate (2025-2033) | 18.9% |
Next generation sequencing (NGS), also known as high-throughput sequencing, is a cutting-edge technology used in molecular biology to determine the precise order of nucleotides (adenine, guanine, cytosine, and thymine) in a DNA or RNA molecule. NGS has revolutionized genomics research, enabling scientists to sequence large volumes of genetic material rapidly and cost-effectively. This technology has numerous applications in fields such as genomics, genetics, personalized medicine, and biomedical research. These platforms can generate vast amounts of sequencing data in a single run. This high throughput is essential for applications like whole-genome sequencing, metagenomics, transcriptomics, and more. There are several NGS platforms available, each with its own technology and chemistry. Some common platforms include Illumina, Ion Torrent (now part of Thermo Fisher Scientific), Pacific Biosciences (PacBio), and Oxford Nanopore Technologies. Each platform has unique advantages and limitations, influencing its suitability for specific applications.
In the United States, the next generation sequencing market has been experiencing robust growth in recent years, driven by the increasing demand for personalized medicine. Healthcare providers and pharmaceutical companies are increasingly relying on NGS to analyze individual patient genomes, enabling the customization of treatment plans and the development of targeted therapies. This approach enhances patient outcomes and reduces healthcare costs by minimizing the use of ineffective treatments. Another significant trend in the market is the expansion of applications beyond healthcare. The technology is now being widely adopted in agriculture and environmental research. Farmers and scientists use NGS to analyze the genetic makeup of crops and livestock, allowing for the development of more resilient and productive agricultural practices. Additionally, environmental researchers use NGS to study ecosystems, track biodiversity, and monitor environmental changes, contributing to our understanding of ecological dynamics and the impact of human activities on the environment. Besides, the adoption of NGS is also being propelled by advancements in automation and data analysis. As sequencing instruments become more automated and user-friendly, the barrier to entry for laboratories and research facilities is lowering. This accessibility, combined with the increasing availability of bioinformatics tools and software, enables a broader range of organizations to harness the power of NGS technology. Furthermore, government initiatives and funding play a pivotal role in driving the NGS market in the United States. Federal agencies, such as the National Institutes of Health (NIH) and the National Human Genome Research Institute (NHGRI), allocate significant resources to support genomics research and the development of NGS technologies. These investments accelerate scientific discoveries and stimulate innovation and economic growth in the biotechnology sector.
IMARC Group provides an analysis of the key trends in each segment of the market, along with forecasts at the country level for 2025-2033. Our report has categorized the market based on sequencing type, product type, technology, application, and end user.
Sequencing Type Insights:
The report has provided a detailed breakup and analysis of the market based on the sequencing type. This includes whole genome sequencing, targeted resequencing, whole exome sequencing, RNA sequencing, chip sequencing, de novo sequencing, methyl sequencing, and others.
Product Type Insights:
A detailed breakup and analysis of the market based on the product type have also been provided in the report. This includes instruments, reagents and consumables, and software and services.
Technology Insights:
The report has provided a detailed breakup and analysis of the market based on the technology. This includes sequencing by synthesis, ion semiconductor sequencing, single-molecule real-time sequencing, nanopore sequencing, and others.
Application Insights:
A detailed breakup and analysis of the market based on the application have also been provided in the report. This includes biomarker and cancer, drug discovery and personalized medicine, genetic screening, diagnostics, agriculture and animal research, and others.
End User Insights:
The report has provided a detailed breakup and analysis of the market based on the end user. This includes academic institutes and research centers, hospitals and clinics, pharmaceutical and biotechnology companies, and others.
Regional Insights:
The report has also provided a comprehensive analysis of all the major regional markets, which include Northeast, Midwest, South, and West.
The market research report has also provided a comprehensive analysis of the competitive landscape. Competitive analysis such as market structure, key player positioning, top winning strategies, competitive dashboard, and company evaluation quadrant has been covered in the report. Also, detailed profiles of all major companies have been provided.
Report Features | Details |
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Base Year of the Analysis | 2024 |
Historical Period | 2019-2024 |
Forecast Period | 2025-2033 |
Units | Billion USD |
Scope of the Report | Exploration of Historical and Forecast Trends, Industry Catalysts and Challenges, Segment-Wise Historical and Predictive Market Assessment:
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Sequencing Types Covered | Whole Genome Sequencing, Targeted Resequencing, Whole Exome Sequencing, RNA Sequencing, CHIP Sequencing, De Novo Sequencing, Methyl Sequencing, Others |
Product Types Covered | Instruments, Reagents and Consumables, Software and Services |
Technologies Covered | Sequencing by Synthesis, Ion Semiconductor Sequencing, Single-Molecule Real-Time Sequencing, Nanopore Sequencing, Others |
Applications Covered | Biomarker and Cancer, Drug Discovery and Personalized Medicine, Genetic Screening, Diagnostics, Agriculture and Animal Research, Others |
End Users Covered | Academic Institutes and Research Centers, Hospitals and Clinics, Pharmaceutical and Biotechnology Companies, Others |
Regions Covered | Northeast, Midwest, South, West |
Customization Scope | 10% Free Customization |
Post-Sale Analyst Support | 10-12 Weeks |
Delivery Format | PDF and Excel through Email (We can also provide the editable version of the report in PPT/Word format on special request) |