Next Generation Sequencing Market Size 2024-2028
The next generation sequencing market size is forecast to increase by USD 4.61 billion, at a CAGR of 14.49% between 2023 and 2028.
The Next Generation Sequencing (NGS) market is experiencing significant growth, driven by the increasing utilization of NGS methods in various applications, including diagnostics, research, and personalized medicine. Advancements in NGS techniques have led to faster and more cost-effective sequencing, enabling broader access to genetic information and fueling innovation in fields such as agriculture, environmental research, and forensics. However, the market faces challenges, primarily in the area of clinical validation for direct-to-consumer genetic tests. As the availability of genetic information expands, ensuring the accuracy and reliability of test results becomes increasingly important. Addressing these concerns through rigorous clinical validation processes and regulatory compliance will be crucial for market participants to build trust and credibility with consumers and healthcare providers. Companies that effectively navigate these challenges and continue to innovate in NGS technology and applications will be well-positioned to capitalize on the market's growth potential.
What will be the Size of the Next Generation Sequencing Market during the forecast period?
Explore in-depth regional segment analysis with market size data - historical 2018-2022 and forecasts 2024-2028 - in the full report.
Request Free SampleThe next generation sequencing (NGS) market continues to evolve, driven by advancements in sequencing platforms and data analysis techniques. Seamlessly integrated solutions are transforming the landscape, connecting entities such as sequence databases, RNA sequencing, targeted sequencing, and NGS applications. Copy number variation and reference genomes are critical components of genome assembly, ensuring quality control and accuracy. Methylation analysis, sequencing platforms, and data analysis are intricately linked, enabling the identification of epigenetic modifications and enhancing genomic understanding. Reproductive genomics, exome sequencing, data visualization, gene expression analysis, forensic genomics, infectious disease genomics, and variant calling are integral parts of the NGS ecosystem.
Sequence alignment, PACBI sequencing, DNA extraction, Ion Torrent sequencing, base calling, and single-cell sequencing are additional techniques expanding the scope of NGS applications. Agricultural genomics, clinical interpretation, library preparation, Illumina sequencing, whole genome sequencing, variant annotation, cancer genomics, mutation detection, read mapping, and microbial sequencing are all areas benefiting from NGS technology. Structural variation and nanopore sequencing are emerging technologies pushing the boundaries of genomic research. The NGS market's continuous dynamism reflects the ongoing unfolding of market activities and evolving patterns, with each entity playing a crucial role in the broader genomic research landscape.
How is this Next Generation Sequencing Industry segmented?
The next generation sequencing industry research report provides comprehensive data (region-wise segment analysis), with forecasts and estimates in 'USD million' for the period 2024-2028, as well as historical data from 2018-2022 for the following segments. End-userAcademic researchClinical researchPharmaceutical and biotechnology companiesOthersProductConsumablesEquipmentGeographyNorth AmericaUSCanadaEuropeGermanyUKAPACChinaRest of World (ROW)
By End-user Insights
The academic research segment is estimated to witness significant growth during the forecast period.The next generation sequencing (NGS) market encompasses various applications and technologies, including RNA sequencing, targeted sequencing, and genome assembly. Academic research institutions, such as universities and research organizations, represent a significant market segment. Researchers in this sector employ NGS for diverse purposes, including drug discovery, personalized medicine, and clinical diagnostics. NGS enables the rapid sequencing of vast genetic data volumes, facilitating the analysis of genetic variations and elucidating disease mechanisms. Key factors fueling the adoption of NGS in academic research include decreasing sequencing costs, user-friendly software, and the growing demand for personalized and precision medicine. NGS applications extend to reproductive genomics, exome sequencing, and gene expression analysis. Data visualization tools and clinical interpretation services aid researchers in making sense of the massive data generated. NGS platforms, such as PacBio sequencing, Ion Torrent sequencing, and Illumina sequencing, cater to different sequencing needs. Library preparation, DNA extraction, and base calling are essential processes in NGS workflows
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The global clinical next-generation sequencing (NGS) data analysis industry is valued at USD 3.17 billion in 2025. It is expected to grow at a CAGR of 17.4% and reach USD 15.77 billion by 2035. Key trends in global clinical NGS data analysis reflect how next-generation sequencing (NGS) has significantly impacted molecular biology. However, the most difficult and time-consuming part of this progress is analyzing the clinical data that comes with NGS.
Metric | Value |
---|---|
Industry Size (2025E) | USD 3.17 billion |
Industry Size (2035F) | USD 15.77 billion |
CAGR (2025 to 2035) | 17.4% |
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Next Generation Sequencing Market size is growing with a CAGR of 7.5% in the prediction period and it crosses USD 7.79 billion by 2032 from USD 4.0 Bn in 2022.
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The next generation sequencing services market size is estimated to grow from USD 12.2 billion to USD 87.5 billion by 2035, representing a CAGR of 21.78%, during the forecast period 2025-2035.
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The global next generation sequencing market size was valued at USD 23.3 Billion in 2024. Looking forward, IMARC Group estimates the market to reach USD 85.4 Billion by 2033, exhibiting a CAGR of 15.5% from 2025-2033. North America currently dominates the market, holding a market share of over 39.7% in 2024. The market for NGS is expanding rapidly due to ongoing technological advancements, increasing use in clinical applications, escalating demand for bioinformatics tools and data analysis solutions, a rising focus on precision medicine, as well as enhanced research and development efforts.
Report Attribute
|
Key Statistics
|
---|---|
Base Year
| 2024 |
Forecast Years
|
2025-2033
|
Historical Years
|
2019-2024
|
Market Size in 2024
| USD 23.3 Billion |
Market Forecast in 2033
| USD 85.4 Billion |
Market Growth Rate 2025-2033 | 15.5% |
IMARC Group provides an analysis of the key trends in each segment of the global next generation sequencing market, along with forecast at the global, regional, and country levels from 2025-2033. The market has been categorized based on sequencing type, product type, technology, application, and end-user.
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Global Next Generation Sequencing Market estimated size and share is estimated to attain USD 39.14 billion by 2034, with a forecasted CAGR of 14.20% during the period.
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The global clinical oncology next-generation sequencing (NGS) market is poised for substantial growth, with its size estimated at USD 744.4 million in 2025 and projected to expand at a robust compound annual growth rate (CAGR) of 17.3% through 2034.
Metric | Value |
---|---|
Industry Size (2025E) | USD 744.4 million |
Industry Value (2035F) | USD 3.13 billion |
CAGR (2025 to 2035) | 17.3% |
Country-wise Insights
Countries | CAGR 2025 to 2035 |
---|---|
France | 21.6% |
United States | 19.4% |
Germany | 19.1% |
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The global Next-Generation Sequencing (NGS) market size reached USD 10.6 Billion in 2024 and is expected to reach USD 35.4 Billion in 2034 registering a CAGR of 12.8%. Next-Generation Sequencing market growth is primarily driven owing to Increasing applications in clinical diagnosis and increase in...
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Global Next Generation Sequencing Market will grow at a CAGR of 14.20% during the forecast period, with an estimated size and share crossing USD 39.14 billion by 2034.
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Next-generation Sequencing (NGS) Market size and share is estimated to be USD 37.8 Billion by 2034, with a CAGR of 13.6% during the forecast period.
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The global Next-Generation Sequencing (NGS) services market size is anticipated to experience significant growth, reaching USD 15.3 billion by 2032, up from USD 4.8 billion in 2023, with a compound annual growth rate (CAGR) of 13.12% from 2024 to 2032. This remarkable expansion is driven by numerous factors, including the increasing demand for personalized medicine, advancements in genomic technologies, and the growing prevalence of genetic disorders. The ability of NGS to provide comprehensive insights into genetic variations and its applications across various sectors further drives market growth. The ongoing research and development activities in genomic studies and the rising adoption of NGS technologies by clinical laboratories are also contributing to the market’s upward trajectory.
One of the primary growth factors in the NGS services market is the escalating demand for personalized medicine. Personalized medicine tailors medical treatment to the individual characteristics of each patient, which has been gaining traction due to its potential for improving patient outcomes and reducing healthcare costs. NGS plays a crucial role in personalized medicine by allowing for the detailed analysis of genetic data, which can lead to more precise diagnoses and more effective treatment plans. The ability of NGS to rapidly and accurately sequence entire genomes or targeted genomic regions is a significant advantage in the development of personalized medical treatments, thus boosting market growth.
Technological advancements in NGS are another significant growth driver. Over the past decade, the cost of sequencing has drastically decreased, making NGS more accessible to a broader range of users, including smaller research facilities and clinics. Improvements in sequencing technologies have led to faster turnaround times, increased throughput, and greater accuracy, which are essential for applications in clinical and research settings. The continuous innovation in sequencing technologies is expected to further fuel the adoption of NGS services, thereby propelling market growth throughout the forecast period.
The growing prevalence of genetic disorders and the increasing focus on early diagnosis and treatment are also contributing to the growth of the NGS services market. Genetic testing using NGS can identify mutations associated with genetic disorders, enabling early intervention and management. As healthcare providers and researchers gain more awareness of the benefits of NGS in diagnosing and treating genetic diseases, the demand for NGS services is expected to rise. Moreover, the potential of NGS to uncover new genetic markers and therapeutic targets in complex diseases such as cancer is driving further investment and adoption in this field.
Regionally, North America dominates the NGS services market due to the region's advanced healthcare infrastructure, significant investments in genomic research, and the presence of key market players. The Asia Pacific region, however, is expected to witness the highest growth rate during the forecast period, driven by increasing investments in healthcare and biotechnology and growing awareness of personalized medicine. Europe also holds a substantial share of the market, supported by strong research initiatives and government funding in genomics. Meanwhile, Latin America and the Middle East & Africa are gradually adopting NGS services as healthcare infrastructure improves and awareness of genomic applications increases.
The technology segment of the NGS services market is a cornerstone for its growth, comprising various advanced sequencing techniques that cater to diverse research and clinical needs. Whole genome sequencing is one of the most comprehensive approaches, allowing for the analysis of the complete DNA sequence of an organism. This technology is pivotal in identifying genetic variations and understanding the genetic basis of diseases. Its ability to provide a complete picture of the genome makes it invaluable for research and clinical diagnostics, driving its demand in both sectors. As costs continue to decrease, whole genome sequencing is becoming more accessible, further broadening its application base and contributing to market growth.
Targeted sequencing, another critical technology in the NGS services market, focuses on specific areas of the genome, allowing for the detailed study of genes of interest. This technology is particularly beneficial in clinical settings where specific mutations or genetic markers are associated with
According to our latest research, the global Next Generation Sequencing (NGS) market size reached USD 13.2 billion in 2024. The market is demonstrating robust expansion, supported by a compound annual growth rate (CAGR) of 16.7% from 2025 to 2033. By the end of 2033, the NGS market is expected to achieve a value of USD 44.2 billion. This impressive growth trajectory is primarily fueled by the increasing adoption of genomic medicine, technological advancements in sequencing platforms, and the expanding scope of NGS applications across clinical diagnostics, drug discovery, and agricultural biotechnology.
The surge in demand for precision medicine and personalized healthcare solutions has been a key driver for the expansion of the Next Generation Sequencing market. Healthcare providers and pharmaceutical companies are leveraging NGS technologies to tailor treatments to individual genetic profiles, resulting in improved patient outcomes and reduced adverse drug reactions. Furthermore, the integration of NGS into routine clinical workflows, particularly in oncology, rare disease diagnostics, and reproductive health, is accelerating the market’s penetration. The growing prevalence of chronic and genetic disorders worldwide further underscores the need for advanced genomic analysis, solidifying the role of NGS as an indispensable tool in modern healthcare.
In addition to healthcare, the NGS market is experiencing significant growth due to its transformative impact on drug discovery and development. Pharmaceutical and biotechnology companies are increasingly utilizing NGS for target identification, biomarker discovery, and pharmacogenomics research. The ability to rapidly sequence entire genomes or exomes enables researchers to identify disease-associated mutations and genetic variations with unprecedented speed and accuracy. This not only shortens the drug development timeline but also enhances the success rate of clinical trials. The expansion of NGS applications into agriculture and animal research, where it is used for crop improvement, disease resistance, and livestock breeding, further broadens the market landscape.
Another critical growth factor for the NGS market is the ongoing technological innovation in sequencing platforms, software, and consumables. The introduction of high-throughput, cost-effective, and user-friendly sequencing systems has democratized access to genomic data, enabling even small research labs and clinics to adopt NGS technologies. Cloud-based bioinformatics solutions and advanced data analytics platforms are addressing the challenges associated with large-scale genomic data interpretation and storage. Additionally, supportive regulatory frameworks and increased funding for genomics research from both public and private sectors are fostering a conducive environment for market expansion. Overall, the synergy between technological advancements, expanding applications, and supportive infrastructure is propelling the NGS market to new heights.
Regionally, North America continues to dominate the Next Generation Sequencing market, accounting for the largest revenue share in 2024. This leadership is attributed to the presence of major market players, advanced healthcare infrastructure, and substantial investments in genomics research. Europe follows closely, driven by robust government initiatives and a growing focus on precision medicine. Meanwhile, the Asia Pacific region is emerging as a high-growth market, fueled by increasing healthcare expenditure, rising awareness of genomic medicine, and expanding research capabilities. Latin America and the Middle East & Africa are also witnessing steady growth, albeit at a slower pace, as they gradually enhance their genomic research and healthcare infrastructure. Collectively, these regional dynamics are shaping the global trajectory of the NGS market, with significant opportunities for growth and innovation across all geographies.
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The global next generation sequencing market is set to witness a growth rate of ~15% in the next 5 years. Rising demand for precision medicine, technological advancements in sequencing platforms, falling costs of sequencing, growing use in clinical diagnostics, expanding applications beyond human genomics, increased government and private funding, are some of the key factors […]
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Next Generation Sequencing (NGS) Market size reached US$ 13.42 Billion in 2024 and is expected to reach US$ 35.92 Billion by 2033
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[195+ Pages Report] Global Next Generation Sequencing market expected to surpass a value of USD 12,624.3 Million by 2026, growing at a CAGR of 16.4% between 2020 and 2026. Major players in the market are Hoffmann-La Roche, Thermo Fisher Scientific Inc., Qiagen, PerkinElmer Inc., Macrogen Inc., Illumina Inc., Eurofins Scientific
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The global Next Generation Sequencing (NGS) kits market size was valued at USD 5.2 billion in 2023 and is projected to reach USD 14.3 billion by 2032, growing at a CAGR of 11.7% during the forecast period. This substantial growth is primarily driven by the increasing adoption of NGS technologies across various applications, such as clinical diagnostics, drug discovery, and agricultural research. The demand for accurate and rapid sequencing methods has led to significant advancements in NGS kit technologies, further fueling market expansion.
One of the key growth factors propelling the NGS kits market is the rising prevalence of genetic disorders and cancers, which necessitate advanced diagnostic tools for early detection and personalized treatment. With the increasing incidence of these diseases, healthcare providers are turning to NGS for its ability to deliver comprehensive genomic data swiftly and accurately. Moreover, the decline in sequencing costs over the years has made these technologies more accessible to a broader range of research and clinical laboratories, thus driving market growth.
Another significant factor contributing to the market's growth is the expanding applications of NGS in various fields such as oncology, reproductive health, and infectious disease research. In oncology, NGS is utilized for tumor profiling, which helps in identifying specific genetic mutations and tailoring personalized treatment plans. In reproductive health, NGS is employed for non-invasive prenatal testing (NIPT) to detect chromosomal abnormalities early in pregnancy. The versatility of NGS technologies in addressing diverse research and clinical needs is a major driver of market expansion.
Technological advancements in NGS kits are also spurring market growth. Innovations such as improvements in sequencing accuracy, speed, and the development of user-friendly platforms are making NGS more efficient and accessible. Companies are investing heavily in R&D to introduce next-generation kits that offer enhanced performance and ease of use. These advancements are expected to reduce the complexity and cost of sequencing, making it a viable option for smaller laboratories and new market entrants.
The Next Generation Sequencing (NGS) kits market can be segmented by product type into DNA Sequencing Kits, RNA Sequencing Kits, Whole Genome Sequencing Kits, Targeted Sequencing Kits, and Others. DNA sequencing kits are among the most widely used products in this market, driven by their essential role in genetic research and diagnostics. These kits are vital for sequencing the complete or partial DNA sequences in a genome, enabling researchers to identify genetic variants associated with diseases. The continuous development of high-throughput DNA sequencing kits has significantly enhanced the speed and accuracy of sequencing, fostering market growth.
RNA Next-Generation Sequencing has emerged as a pivotal tool in the realm of genomics, offering unparalleled insights into the transcriptomic landscape of cells. This technology allows researchers to capture a snapshot of gene expression at a given moment, providing a deeper understanding of cellular functions and disease mechanisms. The ability to sequence RNA with high precision and speed has revolutionized studies in oncology, where understanding the expression profiles of tumors can lead to the identification of novel biomarkers and therapeutic targets. As the demand for personalized medicine grows, RNA Next-Generation Sequencing is becoming increasingly integral in tailoring treatments to individual genetic profiles, thereby enhancing the efficacy of therapeutic interventions.
RNA sequencing kits are another crucial segment in the NGS kits market. These kits are designed to sequence RNA molecules, providing insights into gene expression profiles and transcriptomics. The growing interest in understanding the role of RNA in various biological processes and diseases has led to increased demand for RNA sequencing kits. This segment is particularly important in cancer research, where RNA sequencing helps in understanding tumor biology and identifying potential therapeutic targets. The advancements in RNA sequencing technologies, such as single-cell RNA sequencing, are expected to drive further
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This report examines the markets for next generation sequencing (NGS) diagnostics for the years 2012, 2013 and 2018.
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The global market size for Next-Generation Sequencing (NGS) data analysis was valued at $1.8 billion in 2023 and is expected to reach $8.5 billion by 2032, exhibiting a robust CAGR of 18.7% during the forecast period. The growth of this market can be attributed to advancements in sequencing technologies, increasing applications in various fields like clinical diagnostics and personalized medicine, and the rising prevalence of genetic disorders and cancer.
One of the primary growth factors driving the NGS data analysis market is the increasing adoption of NGS technologies in clinical diagnostics. With the advent of precision medicine, healthcare providers are increasingly relying on genomic data to tailor treatments to individual patients' genetic profiles. This has necessitated sophisticated data analysis tools to interpret the enormous amounts of data generated by NGS, thereby driving the demand for advanced software and services. Furthermore, the declining cost of sequencing has made NGS more accessible, leading to its widespread adoption across various medical and research domains.
Another significant growth factor is the rising investment in research and development by pharmaceutical and biotechnology companies. These companies are leveraging NGS data analysis for drug discovery and development, aiming to identify genetic markers and understand the molecular basis of diseases. The ability to analyze large-scale genomic data is crucial for identifying potential drug targets and biomarkers, which can accelerate the development of new therapies. Additionally, government funding and initiatives to promote genomic research are further propelling the market's growth.
The expanding applications of NGS data analysis beyond human healthcare also contribute to market growth. In agriculture, NGS is used for crop improvement and animal breeding, helping to enhance yield, disease resistance, and nutritional quality. Similarly, NGS is applied in environmental research to study biodiversity and monitor ecological changes. These diverse applications underscore the versatility of NGS technologies and the growing need for robust data analysis solutions to handle complex datasets across different fields.
In terms of regional outlook, North America is expected to dominate the NGS data analysis market due to its well-established healthcare infrastructure, high R&D investment, and early adoption of advanced technologies. Europe follows closely, driven by significant research initiatives and collaborations in genomic studies. The Asia Pacific region is anticipated to witness the highest growth rate, fueled by increasing healthcare expenditure, growing awareness of precision medicine, and expanding genomic research activities. Latin America and the Middle East & Africa regions are also showing promising growth, albeit at a slower pace, as they ramp up their healthcare and research capabilities.
The Next-Generation Sequencing data analysis market can be segmented by product type into software and services. Software solutions are crucial for managing, analyzing, and interpreting the vast amounts of data generated by NGS platforms. These software tools include bioinformatics applications, data visualization tools, and genomic analysis platforms. The increasing complexity of NGS data and the need for high-throughput analysis have driven the demand for advanced software solutions that can handle large datasets efficiently and accurately.
Within the software segment, bioinformatics software holds a significant share due to its essential role in data processing and interpretation. These tools enable researchers to align sequences, identify genetic variants, and perform functional annotation. The continuous evolution of bioinformatics algorithms and the integration of artificial intelligence and machine learning techniques have enhanced the capabilities of these software solutions, making them indispensable for NGS data analysis. Additionally, cloud-based bioinformatics platforms are gaining traction, offering scalability, flexibility, and cost-effectiveness to users.
The services segment encompasses various offerings, including data analysis services, consulting, and training. As the demand for NGS data analysis grows, many organizations prefer outsourcing these tasks to specialized service providers. These providers offer expertise in bioinformatics, data interpretation, and report generation, helping researchers and clinicians make sense of the complex
This statistic shows the projected size of the DNA next generation sequencing market worldwide from 2023 to 2033. In 2023, the market was valued at around 9.2 billion U.S. dollars, with forecasts predicting that the size will increase to some 66 billion dollars by 2033.
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The global next-generation sequencing market is estimated to grow $4.14 billion in 2016 and is estimated to grow over $11.92 billion by 2024. This report studies the market analysis, size, growth, trends and forecast.
Next Generation Sequencing Market Size 2024-2028
The next generation sequencing market size is forecast to increase by USD 4.61 billion, at a CAGR of 14.49% between 2023 and 2028.
The Next Generation Sequencing (NGS) market is experiencing significant growth, driven by the increasing utilization of NGS methods in various applications, including diagnostics, research, and personalized medicine. Advancements in NGS techniques have led to faster and more cost-effective sequencing, enabling broader access to genetic information and fueling innovation in fields such as agriculture, environmental research, and forensics. However, the market faces challenges, primarily in the area of clinical validation for direct-to-consumer genetic tests. As the availability of genetic information expands, ensuring the accuracy and reliability of test results becomes increasingly important. Addressing these concerns through rigorous clinical validation processes and regulatory compliance will be crucial for market participants to build trust and credibility with consumers and healthcare providers. Companies that effectively navigate these challenges and continue to innovate in NGS technology and applications will be well-positioned to capitalize on the market's growth potential.
What will be the Size of the Next Generation Sequencing Market during the forecast period?
Explore in-depth regional segment analysis with market size data - historical 2018-2022 and forecasts 2024-2028 - in the full report.
Request Free SampleThe next generation sequencing (NGS) market continues to evolve, driven by advancements in sequencing platforms and data analysis techniques. Seamlessly integrated solutions are transforming the landscape, connecting entities such as sequence databases, RNA sequencing, targeted sequencing, and NGS applications. Copy number variation and reference genomes are critical components of genome assembly, ensuring quality control and accuracy. Methylation analysis, sequencing platforms, and data analysis are intricately linked, enabling the identification of epigenetic modifications and enhancing genomic understanding. Reproductive genomics, exome sequencing, data visualization, gene expression analysis, forensic genomics, infectious disease genomics, and variant calling are integral parts of the NGS ecosystem.
Sequence alignment, PACBI sequencing, DNA extraction, Ion Torrent sequencing, base calling, and single-cell sequencing are additional techniques expanding the scope of NGS applications. Agricultural genomics, clinical interpretation, library preparation, Illumina sequencing, whole genome sequencing, variant annotation, cancer genomics, mutation detection, read mapping, and microbial sequencing are all areas benefiting from NGS technology. Structural variation and nanopore sequencing are emerging technologies pushing the boundaries of genomic research. The NGS market's continuous dynamism reflects the ongoing unfolding of market activities and evolving patterns, with each entity playing a crucial role in the broader genomic research landscape.
How is this Next Generation Sequencing Industry segmented?
The next generation sequencing industry research report provides comprehensive data (region-wise segment analysis), with forecasts and estimates in 'USD million' for the period 2024-2028, as well as historical data from 2018-2022 for the following segments. End-userAcademic researchClinical researchPharmaceutical and biotechnology companiesOthersProductConsumablesEquipmentGeographyNorth AmericaUSCanadaEuropeGermanyUKAPACChinaRest of World (ROW)
By End-user Insights
The academic research segment is estimated to witness significant growth during the forecast period.The next generation sequencing (NGS) market encompasses various applications and technologies, including RNA sequencing, targeted sequencing, and genome assembly. Academic research institutions, such as universities and research organizations, represent a significant market segment. Researchers in this sector employ NGS for diverse purposes, including drug discovery, personalized medicine, and clinical diagnostics. NGS enables the rapid sequencing of vast genetic data volumes, facilitating the analysis of genetic variations and elucidating disease mechanisms. Key factors fueling the adoption of NGS in academic research include decreasing sequencing costs, user-friendly software, and the growing demand for personalized and precision medicine. NGS applications extend to reproductive genomics, exome sequencing, and gene expression analysis. Data visualization tools and clinical interpretation services aid researchers in making sense of the massive data generated. NGS platforms, such as PacBio sequencing, Ion Torrent sequencing, and Illumina sequencing, cater to different sequencing needs. Library preparation, DNA extraction, and base calling are essential processes in NGS workflows