Global Next Generation Sequencing Market Size, Segmentation, Trends and Growth Analysis Forecast by 2031

Next Generation Sequencing Market Overview and Analysis:

The Next-generation Sequencing Market size is estimated at USD 12.12 billion in 2023 and is expected to register a CAGR of 14.5% during the forecast period (2024-2031).

Next Generation Sequencing (NGS), or high-throughput sequencing, is a cutting-edge technology that revolutionizes the process of determining DNA or RNA sequences. It enables the parallel sequencing of millions of fragments, providing rapid and cost-effective large-scale sequencing compared to traditional methods. NGS platforms, such as Illumina, Ion Torrent, PacBio, and Oxford Nanopore, offer high throughput and versatility, making them applicable in diverse areas such as whole-genome sequencing, transcriptome analysis, and metagenomics. The technology's efficiency has significantly lowered the cost per base, facilitating extensive genomic studies and contributing to breakthroughs in personalized medicine, cancer research, and various biological fields, accelerating our understanding of genetic information and its implications.

The market for Next Generation Sequencing (NGS) is anticipated to experience substantial growth due to several key factors. Notably, the expanding applications in clinical diagnosis, driven by NGS's ability to provide comprehensive genetic information, are expected to be a significant catalyst for market expansion. The speed, cost-effectiveness, and accuracy offered by NGS technologies further contribute to their increasing adoption, especially when compared to traditional methods like microarrays. Additionally, the rising efficiency of NGS platforms has positioned them as preferred tools in various applications, particularly in drug discovery, where their capabilities play a crucial role. This shift towards NGS is not only driven by its superior performance but also by the growing limitations of conventional technologies. As a result, the market is poised to benefit from the convergence of these factors, propelling NGS to the forefront of genetic analysis and molecular diagnostics.

Market Segmentation: The Global Next-Generation Sequencing Market is Segmented by Type of Sequencing (Whole Genome Sequencing, Targeted Resequencing, Whole Exome Sequencing, RNA Sequencing, CHIP Sequencing, De Novo Sequencing, and Methyl Sequencing), Product Type (Instruments, Reagents, and Consumables, and Services), End User (Hospitals and Healthcare Institutions, Academics, and Pharmaceutical and Biotechnology Companies) Application (Drug Discovery and Personalized Medicine, Genetic Screening, Diagnostics, Agriculture and Animal Research, and Other Applications), and Geography (North America, Europe, Asia-Pacific, Middle East and Africa, and South America). The market size and forecast are provided in terms of values in USD million for all the above-mentioned segments.

Next-Generation Sequencing Market Trends:

The Next Generation Sequencing (NGS) market is witnessing several prominent trends that are shaping its trajectory. One notable trend is the increasing integration of NGS in clinical diagnostics, fueled by its ability to provide comprehensive genomic information. This is particularly significant as precision medicine gains prominence, driving the demand for more accurate and personalized healthcare solutions. The ongoing advancements in NGS technologies, marked by improvements in speed, cost-efficiency, and accuracy, are further propelling market growth. As NGS continues to outperform traditional sequencing methods such as Sanger sequencing and microarrays, researchers and healthcare professionals are increasingly adopting these advanced platforms. Moreover, the expanding applications of NGS in areas like oncology, rare disease diagnosis, and infectious disease research contribute to the market's upward trajectory. Additionally, the growing trend of using NGS in drug discovery and development processes underscores its pivotal role in advancing pharmaceutical research. These trends collectively indicate a dynamic and promising landscape for the NGS market, emphasizing its critical role in driving advancements across various scientific and medical domains.

Market Drivers:

Increasing Applications in Clinical Diagnosis and Speed, Cost, and Accuracy

The surge in next-generation sequencing (NGS) applications for clinical diagnosis represents a pivotal trend, particularly in precision medicine, where NGS expeditiously deciphers the genetic basis of diseases, revolutionizing diagnostic processes. NGS's remarkable speed in analyzing extensive genetic data addresses time constraints in urgent clinical scenarios, facilitating quicker and more informed decision-making. Cost-effectiveness is a key driver, as reduced per-base sequencing costs make large-scale genomic studies and personalized medicine economically viable, broadening access to advanced genetic diagnostics. Furthermore, NGS's precision in detecting genetic variations enhances its reliability in identifying disease-related markers, contributing to accurate clinical decision-making, personalized treatment plans, and predicting individual responses to therapies. This convergence of clinical applications, speed, cost-efficiency, and accuracy underscores NGS's transformative impact on modern healthcare, promising to revolutionize diagnostics and enhance patient outcomes across diverse medical conditions.

Increasing Efficiency when Compared To Traditional Technologies Such As Microarrays and Rising Drug Discovery Applications

The escalating efficiency of next-generation sequencing (NGS) compared to traditional technologies, such as microarrays, marks a paradigm shift in genomic research. NGS's ability to simultaneously sequence millions of DNA fragments in a massively parallel manner significantly accelerates the pace of data generation, surpassing the throughput of microarray technologies. This increased efficiency translates into quicker and more comprehensive insights into the genetic landscape. NGS's versatility and capacity to provide high-throughput data have led to its widespread adoption in various applications, with drug discovery standing out prominently. The rising number of drug discovery applications underscores NGS's role in identifying potential therapeutic targets, elucidating molecular mechanisms, and comprehensively characterizing genetic variations associated with diseases. The efficiency gains in data generation and analysis afforded by NGS contribute to a more agile and effective drug development process, ultimately fostering advancements in personalized medicine and targeted therapies. As a result, NGS's superior efficiency in comparison to traditional technologies propels its position as a transformative tool in genomics, with far-reaching implications for both research and therapeutic innovation.

Market Restraints:

Interpretation of Complex Data and Lack of Skilled Professionals

The rapid growth of the Next Generation Sequencing (NGS) market is not without its challenges, as the interpretation of complex data and the shortage of skilled professionals pose significant hurdles. The vast amount of genomic information generated by NGS requires sophisticated bioinformatics tools and expertise for accurate analysis and interpretation. The complexity of genomic data, including identification of variants, structural variations, and understanding their clinical significance, demands advanced computational skills and a deep understanding of genomics. The shortage of professionals with these specialized skills creates a bottleneck in the efficient utilization of NGS technologies, hindering the realization of its full potential. Furthermore, the lack of standardized practices for data interpretation and reporting adds another layer of complexity. Variability in interpretation methodologies across different laboratories and institutions can lead to inconsistencies in results, impacting the reliability and reproducibility of NGS findings. Standardizing interpretation guidelines is essential to ensure consistency and improve the reliability of NGS data across diverse clinical and research settings. Addressing these challenges requires concerted efforts in training and education to produce a skilled workforce capable of handling the intricacies of NGS data analysis. Additionally, ongoing advancements in bioinformatics tools, artificial intelligence, and machine learning are playing a crucial role in automating certain aspects of data interpretation, easing the burden on human analysts.

COVID-19 Impact on Next Generation Sequencing Market:

The diagnostic potential of Next Generation Sequencing (NGS) technology proved instrumental during the COVID-19 pandemic, enabling scientists to decipher the genetic sequence of the virus and unravel the intricacies of mutations. Governments worldwide collaborated with the private sector to swiftly introduce NGS technology into the market as a viable diagnostic tool to combat the pandemic. Notably, an article published by Frontiers in March 2022 highlighted the pivotal role of NGS in studying COVID-19, facilitating a more accessible understanding of the origins of SARS-CoV-2. The technology played a crucial role in investigating the potential origins and mechanisms of the virus, aiding in the formulation of effective strategies to curb the spread of COVID-19 and enhance treatment plans. Consequently, the utilization of NGS technology experienced a significant upsurge throughout the pandemic. Looking ahead, as the world transitions into a post-pandemic phase, the NGS market is anticipated to exhibit stable growth during the forecast period. The lasting impact of NGS in infectious disease research and diagnostics is expected to contribute to its continued adoption and development in various applications beyond the immediate challenges posed by the pandemic.

Segmental analysis:

Whole Genome Sequencing Segment is Expected to Witness Significant Growth Over the Forecast Period

Whole Genome Sequencing (WGS) represents a revolutionary approach in genomics, enabling the comprehensive analysis of an organism's entire DNA. This advanced sequencing technique involves deciphering the complete set of genetic instructions encoded in an individual's or organism's genome. WGS provides a detailed blueprint of the entire DNA sequence, including protein-coding genes, non-coding regions, and structural variations. The significance of WGS lies in its ability to uncover rare and common genetic variants, offering unparalleled insights into an individual's genetic makeup and potential predispositions to diseases. This comprehensive genomic information has transformative implications for personalized medicine, as it allows for a deeper understanding of genetic factors influencing health and disease. WGS has been instrumental in advancing research across various fields, including clinical genetics, cancer genomics, and population studies. Although the technique has become more accessible over time, challenges such as data interpretation and the management of large datasets persist. As technology continues to evolve, whole genome sequencing holds immense promise for revolutionizing healthcare, diagnosis, and treatment strategies by tailoring medical interventions to an individual's unique genetic profile.

Instruments Sequencing Segment is Expected to Witness Significant Growth Over the Forecast Period

In the realm of genomics, a diverse array of instruments is employed for DNA sequencing, each contributing to the rapid advancements in genomic research. High-throughput sequencing technologies, commonly known as Next Generation Sequencing (NGS), have emerged as the forefront instruments driving genomics forward. Illumina sequencers, a prominent example, utilize sequencing-by-synthesis technology, allowing for the parallel sequencing of millions of DNA fragments. The Ion Torrent platform, on the other hand, employs semiconductor sequencing, measuring changes in pH as nucleotides are incorporated during DNA synthesis. PacBio's Single Molecule, Real-Time (SMRT) sequencing stands out for its long-read capabilities, capturing contiguous stretches of DNA, which is particularly valuable in resolving complex genomic regions. Oxford Nanopore Technologies utilizes nanopore-based sequencing, allowing real-time analysis of DNA and RNA by measuring changes in electrical current as molecules pass through a nanopore. These instruments collectively contribute to diverse sequencing applications, from whole genome sequencing to targeted gene panels and transcriptome analysis. As technology continues to evolve, these sequencing instruments play a pivotal role in unlocking the intricacies of the genome, propelling genomics into an era of unprecedented discovery and personalized healthcare.

Hospitals and Healthcare Institutions Segment is Expected to Witness Significant Growth Over the Forecast Period

The integration of Next Generation Sequencing (NGS) technology into hospital settings has ushered in a transformative era in healthcare, offering unprecedented capabilities for genomic analysis and personalized medicine. NGS is increasingly becoming a valuable tool in hospitals for various applications, ranging from diagnostics and disease monitoring to treatment selection based on individual genetic profiles. One notable application is in the field of oncology, where NGS is utilized to characterize the genomic landscape of tumors, identify potential therapeutic targets, and tailor treatment strategies to the specific genetic makeup of each patient. In the context of rare diseases, NGS aids in the identification of genetic mutations responsible for these conditions, enabling timely and accurate diagnoses. Moreover, NGS plays a crucial role in pharmacogenomics, helping healthcare providers optimize drug selection and dosage based on an individual's genetic predispositions. The adoption of NGS in hospitals is facilitated by advancements in technology that have reduced costs and improved turnaround times, making genomic analysis more accessible for routine clinical use. This integration enhances the precision and efficacy of medical interventions, ultimately leading to better patient outcomes. Additionally, the ongoing expansion of NGS applications in hospital settings aligns with the broader trend of transitioning towards precision medicine, where treatments are tailored to an individual's unique genetic characteristics. Despite the promising benefits, challenges such as data interpretation, standardization of protocols, and the need for specialized expertise in genomics remain. As hospitals continue to embrace NGS, efforts are underway to address these challenges and fully unlock the potential of genomic information in improving patient care and advancing medical research within the healthcare setting.

Drug Discovery and Personalized Medicine Segment is Expected to Witness Significant Growth Over the Forecast Period

Next Generation Sequencing (NGS) has emerged as a groundbreaking technology in the realms of drug discovery and personalized medicine, revolutionizing the way researchers and clinicians approach these critical areas of healthcare. In drug discovery, NGS plays a pivotal role in identifying potential therapeutic targets, understanding disease mechanisms, and optimizing drug development processes. The technology allows for comprehensive genomic profiling, enabling researchers to uncover genetic variations associated with diseases, identify biomarkers, and predict drug responses. This information is invaluable in the development of targeted therapies, enhancing the efficiency and success rates of drug discovery initiatives. In the realm of personalized medicine, NGS facilitates a deeper understanding of individual genetic makeup, allowing for tailored medical interventions based on a person's unique genetic profile. By analyzing the entire genome or specific gene panels, NGS provides insights into an individual's predisposition to certain diseases, response to medications, and potential adverse reactions. This information empowers clinicians to make informed decisions about treatment plans, drug selection, and dosage, thereby optimizing therapeutic outcomes and minimizing adverse effects. The integration of NGS into drug discovery and personalized medicine has been particularly transformative in the field of oncology. NGS enables the identification of specific genetic mutations driving cancer growth, guiding the development of targeted therapies that are more precise and effective. This shift towards precision medicine, facilitated by NGS, represents a paradigm shift in healthcare, moving away from a one-size-fits-all approach to treatments tailored to the unique genetic characteristics of each patient. While the adoption of NGS in drug discovery and personalized medicine has been substantial, challenges such as data analysis, standardization, and ethical considerations persist. Nonetheless, ongoing advancements in NGS technologies and bioinformatics are addressing these challenges, paving the way for even greater contributions of NGS to the advancement of drug discovery and the realization of personalized medicine's full potential.

North America Region is Expected to Witness Significant Growth Over the Forecast Period

North America is poised to maintain a substantial share in the next-generation sequencing (NGS) market, with the trend expected to persist in the coming years. The increasing adoption of NGS technology as a routine clinical diagnostic test is driven by factors such as the growing prevalence of chronic and infectious diseases, heightened investments in genomics, and notable advancements by key market players. For instance, the rising incidence of diseases like leukemia, as reported by the Canada Cancer Society and the American Cancer Society, underscores the increasing use of NGS technology-based devices in the region. Additionally, a surge in genomics research spending, exemplified by the National Institutes of Health's projection of an increase from USD 1,160 million in 2021 to USD 1,220 million in 2022 for cancer genomics in the United States, is anticipated to further propel the market. Key market players' strategic moves, such as Predicine, Inc.'s breakthrough device designation for its NGS assay and Thermo Fisher Scientific's FDA approval for the Oncomine Dx Target Test, also contribute to market growth. These developments, combined with the ongoing efforts and investments, are expected to foster the expansion of the NGS market in North America.

Next Generation Sequencing Market Competitive Landscape:

The market for next-generation sequencing (NGS) exhibits a high degree of fragmentation, featuring numerous global and international players. In order to fortify their market presence, key players within the industry are deploying diverse growth strategies. These strategies encompass partnerships, agreements, collaborations, new product launches, geographical expansions, as well as mergers and acquisitions. By engaging in strategic collaborations, companies aim to leverage complementary strengths and expertise, fostering innovation and expanding their market reach. Simultaneously, the introduction of new products and technologies enhances their competitive edge, addressing evolving customer needs. Geographical expansions serve as a means to tap into emerging markets and cater to a broader customer base. Moreover, mergers and acquisitions provide opportunities for consolidation, enabling companies to streamline operations and access new capabilities. This dynamic landscape underscores the competitive nature of the NGS market, with key players actively shaping the industry through a spectrum of strategic initiatives. Some of the key market players working this market are:

• Agilent Technologies
• Bio-Rad Laboratories Inc.
• DNASTAR Inc.
• Eurofins Scientific
• F. Hoffmann-La Roche Ltd.
• Illumina Inc.
• Macrogen Inc.
• Pacific Biosciences of California Inc.
• PerkinElmer Inc.
• Qiagen
• Thermo Fisher Scientific Inc.
• CD Genomics

Recent Development:

1) In January 2023, QIAGEN revealed a strategic collaboration with Helix, a leading population genomics company based in California. The primary objective of this partnership is to propel the development of next-generation sequencing (NGS) companion diagnostics focused on hereditary diseases. This joint effort signifies a concerted approach to leverage QIAGEN's expertise alongside Helix's leadership in population genomics to advance precision medicine and genetic testing.

2) In March 2023, SOPHiA GENETICS, a prominent player in the genomics industry, announced a significant partnership with QIAGEN. This collaboration aims to integrate QIAseq reagent technology with the DDM platform, enhancing the capabilities of tumor analysis through next-generation sequencing (NGS). By combining SOPHiA GENETICS' advanced analysis platform with QIAGEN's cutting-edge reagent technology, the collaboration seeks to bolster the efficiency and accuracy of NGS in dissecting molecular information from tumors. The partnership underscores the industry's commitment to innovation, as it harnesses the synergies between leading companies to drive advancements in genomics and oncology research, ultimately benefiting patients and clinicians alike.

Frequently Asked Questions (FAQ) :

Q1. What was the Next Generation Sequencing Market size in 2023?

Q2. At what CAGR is the Next-generation Sequencing market projected to grow within the forecast period?

Q3. What are the Growth Drivers of the Next-generation Sequencing Market?

Q4. What segments are covered in the Next-generation Sequencing Market Report?