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Next-Generation Sequencing Market Size & Forecast 2025–2033 | CAGR 18.16%

The next-generation sequencing market is expected to grow from US$ 3.76 billion in 2024 to US$ 56.25 billion by 2033, at a CAGR of 18.16%. Growth is driven by genomic research, precision medicine, and rising adoption in diagnostics, oncology, and genetic screening, supported by technological innovation.
Published 13 August 2025

Next Generation Sequencing Market Analysis

The global Next Generation Sequencing Market is anticipated to increase to US$ 56.25 billion by 2033 at a CAGR of 18.16% from 2025 to 2033. This acceleration is driven by advances in genomic studies, greater application in precision medicine, and higher adoption for disease diagnosis, oncology, and genetic testing, as well as technological advancements and diminishing sequencing costs.

Next Generation Sequencing Market Outlook

Next Generation Sequencing (NGS) is a collection of cutting-edge sequencing technologies that enable the fast and affordable sequencing of DNA and RNA. In contrast to Sanger sequencing, which sequences one fragment at a time, NGS has the capacity to sequence millions of fragments in parallel, generating enormous quantities of data per experiment. High-throughput capabilities make it possible for scientists to probe genomes, transcriptomes, and epigenomes in record time with unprecedented precision.

NGS has transformed different disciplines such as genomics, personalized medicine, and oncology. Its applications extend from the identification of genetic variants linked to disease, to the direction of targeted treatments on the basis of a person's genetic profile. NGS is also central to disciplines such as microbiology for metagenomics and in agriculture for improving crops.

The demand for NGS has increased dramatically with its low costs, reduced turnaround times, and capability to solve complex biological queries. As technology is continuously improving, NGS is becoming a core instrument in research and clinic setup that fuels healthcare and life sciences innovations.

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Market Trends for the Next Generation Sequencing Market


Increased Use in Clinical Diagnostics

Next Generation Sequencing (NGS) is being progressively incorporated into clinical diagnostics for the early detection of diseases, notably in oncology, rare genetic diseases, and infectious diseases. The capacity to sequence complete genomes at rapid and affordable speeds has revolutionized personalized medicine, and physicians are now able to customize treatments according to a patient's genetic profile. Diagnostic labs and hospitals are embracing NGS for extensive genetic screening, prenatal screening, and pathogen identification. This trend is sustained by declining sequencing costs and approval of clinical-grade NGS tests from regulators, making it increasingly possible for regular healthcare uses.

Expansion of Liquid Biopsy Applications

Application of NGS in liquid biopsy is proving to be a game-changer in non-invasive cancer diagnosis and monitoring. Liquid biopsy employs circulating tumor DNA (ctDNA) detected in blood samples to facilitate early diagnosis, choice of therapy, and monitoring of real-time treatment response. NGS provides excellent sensitivity in the detection of rare mutations and tumor heterogeneity. The methodology reduces the demand for invasive tissue biopsies, enhancing patient comfort and compliance. With ongoing research, liquid biopsy is being applied to other illnesses, including cardiovascular and infectious diseases, adding to the demand for NGS platforms. February 2022, Invitae Corporation released LiquidPlex Dx and FusionPlex Dx in Europe. It enables genomic profiling together with companion diagnostics utilized for solid tumor neoplasms. They are applied on Illumina's Next Generation Sequencing platforms to perform IVD testing.

Integration with Artificial Intelligence and Big Data

Artificial intelligence and big data analytics are increasingly being incorporated into NGS workflows to improve accuracy, velocity, and interpretation of difficult genomic data. AI-driven tools assist to identify mutations, gene variants, and disease associations more quickly, enabling precision medicine programs. Big data platforms enable scientists to analyze huge genomic datasets for population-scale research, drug development, and biomarker discovery. With increasing sequencing volumes, AI-based solutions are becoming increasingly essential to handle, store, and retrieve actionable insights, bringing down analysis time from weeks to hours. February 2022, Agilent Technologies, Inc. entered into a collaboration with Element Biosciences, Inc. to combine the latter's AVITI System with Agilent's SureSelect target enrichment panels to provide better customer access to genomic tools.

Accelerated Development of Long-Read Sequencing Technologies

Though short-read sequencing is the current market leader, long-read sequencing technologies are increasingly popular due to their capability to resolve multifaceted genomic areas, structural variations, and repeating sequences. Long-read platforms, like those provided by PacBio and Oxford Nanopore, offer greater accuracy in the assembly of genomes and analysis of transcriptomes. These technologies are especially useful in plant genomics, metagenomics, and investigations of rare diseases. Continuing innovation is increasing read length, accuracy, and cost-effectiveness, positioning long-read sequencing as a complement to current NGS approaches both in research and clinical applications.

Growth Drivers in the Next Generation Sequencing Market


Dropping Sequencing Costs

The price for sequencing a human genome has come down significantly in the last decade, and NGS is now more affordable to researchers, clinicians, and diagnostic labs. The downward price trend is pushing adoption in a broader range of applications from discovery research to personalized medicine. Low-cost sequencing facilitates large-scale genomic research, clinical diagnosis, and population genomics initiatives. It also prompts smaller and medium-sized labs to incorporate NGS into their workflow, driving market expansion in the world.

Growing Need for Precision Medicine

NGS is at the heart of precision medicine through the delivery of in-depth genomic information that directs targeted therapy and individualized treatment regimens. In cancer, for instance, tumor DNA sequencing is used to choose the best medicine and track resistance emergence. Governments, healthcare organizations, and drug firms are pouring money into precision medicine programs, propelling the use of NGS. With increasing recognition of personalized medicine, NGS will be an accepted part of patient management, fueling long-term growth in the marketplace.

Increasing Applications in Agricultural and Environmental Genomics

Outside of healthcare, NGS is increasingly used in agriculture for improving crops, resistance to disease, and breeding livestock. Environmental sciences utilize NGS for studying biodiversity, microbial communities, and ecological monitoring. Such uses are broadening the NGS market beyond classical biomedical applications. Sequencing cost-effectively different organisms underpins sustainability programs, food security measures, and climate change research, creating new revenue streams for sequencing services providers.

Sequencing Platforms and Reagent Advances

Ongoing innovation in sequencing hardware, chemistry, and bioinformatics software is increasing NGS speed, accuracy, and capacity. New platforms provide greater throughput and easier workflows, decreasing turnaround time for both research and clinical testing. Better library preparation kits, reagents, and automation systems are facilitating the sequencing process. These developments are reducing barriers to entry for new users while opening up the scope of possible applications, from single-cell sequencing to large-scale population genomics.

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North America Next Generation Sequencing Market

The North America NGS market is a world leader, backed by cutting-edge healthcare infrastructure, good research funding, and a high density of biotech firms. The region enjoys immense government investments in genomic research as well as precision medicine efforts. The U.S. leads on the back of its powerful network of academic institutions, hospitals, and private research labs embracing NGS for diagnostics, oncology, and infectious disease testing. Canada is also increasing its capability by genomics research programs. Strong awareness, technological advancement, and beneficial reimbursement policies further enhance market growth in North America.

Next Generation Sequencing Market in United States

United States is the biggest NGS market in the world, supported by early adoption of innovative genomic technologies and a well-developed biotech ecosystem. The nation has widespread applications in clinical diagnostics, cancer research, pharmaceutical development, and agricultural genomics. Government programs such as the Precision Medicine Program and investments by the private sector drive market growth. Major NGS platform providers, along with academia-industry partnerships, expedite innovation. Consistent regulatory frameworks and increasing demand for personalized care promise continued growth in the U.S. NGS market. February 2025 - Roche introduced its revolutionary sequencing by expansion (SBX) technology, launching a new category of next-generation sequencing. This very fast, high-throughput technology incorporates flexible and scalable SBX chemistry with innovative sensor module, which is ideal for diverse applications.

Next Generation Sequencing Market in India

India's NGS market is growing very fast, fueled by expanding adoption of NGS in clinical diagnostics, genetic research, and agriculture. Although India's NGS market is presently in an earlier stage than established markets, India is experiencing growing demand for NGS in cancer, infectious disease diagnosis, and prenatal diagnosis. Government-supported genomic initiatives, as well as investments made by the private sector, are increasing capabilities and infrastructure. The expanding biotech industry, the availability of qualified professionals, and falling sequencing costs are making NGS accessible. This is supplemented by India's emphasis on personalized medicine and population genomics efforts. At the August 2024 Illumina India Genomics Summit, Illumina announced opening a Global Capability Center in Bengaluru to bolster its technology talent for a global customer base.

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