Global Clinical Oncology Next Generation Sequencing Market Growth, Share, Size, Trends and Forecast (2025 - 2031)
By Technology;
Whole Genome Sequencing, Whole Exome Sequencing, and Targeted Sequencing & Resequencing.By Workflow;
NGS Pre-Sequencing, NGS Sequencing, and NGS Data Analysis.By Application;
Screening, Companion Diagnostics, and Others.By End Use;
Hospitals, Clinics, and Laboratories.By Geography;
North America, Europe, Asia Pacific, Middle East and Africa and Latin America - Report Timeline (2021 - 2031).Introduction
Global Clinical Oncology Next Generation Sequencing Market (USD Million), 2021 - 2031
In the year 2024, the Global Clinical Oncology Next Generation Sequencing Market was valued at USD 906.01 million. The size of this market is expected to increase to USD 2,366.33 million by the year 2031, while growing at a Compounded Annual Growth Rate (CAGR) of 14.7%.
Next-generation sequencing (NGS) is a powerful parallel sequencing technique renowned for its ultra-high throughput, rapid speed, and scalability in deciphering the nucleotide order across entire genomes. In clinical oncology, NGS has revolutionized personalized cancer treatment by enabling the identification of novel and rare cancer mutations, detecting familial cancer predispositions, and providing the genetic basis for optimal targeted therapies. A pivotal stage in the sequencing process is DNA pre-sequencing, where the material is prepared for subsequent sequencing reactions.
Our platform analyzes raw NGS data for each genotype-drug combination, enabling doctors to classify and interpret genomic changes in conjunction with experimental and approved medications. Consequently, NGS data processing systems are increasingly employed in personalized oncology care, facilitating tailored treatment strategies based on individual genetic profiles and improving patient outcomes.
Global Clinical Oncology Next Generation Sequencing Market Recent Developments
-
In March 2022, Vela Diagnostics launched its new OncoKey SL 60 and 525 Plus Panels. These next-generation sequencing (NGS)-based panels are intended to detect DNA and RNA cancer biomarkers from formalin-fixed paraffin-embedded (FFPE) tissue specimens for up to 64 samples in a single sequencing run.
-
In March 2022, Illumina, Inc. launched the TruSight Oncology (TSO) Comprehensive (EU), a single test that assesses multiple tumor genes and biomarkers to reveal the specific molecular profile of a patient's cancer.
Segment Analysis
The Technology segment includes various NGS technologies such as sequencing by synthesis (SBS), ion semiconductor sequencing, and single-molecule real-time sequencing. Sequencing by synthesis, which is widely used for its high accuracy and reliability, dominates the market. Ion semiconductor sequencing and single-molecule real-time sequencing are gaining traction due to their faster processing times and cost-effectiveness, making them appealing for clinical oncology applications. These technologies enable precise genetic analysis for oncology, playing a vital role in the diagnosis and treatment of cancer.
By Workflow, the market is divided into sample preparation, sequencing, data analysis, and interpretation. Sample preparation is a crucial step that involves the extraction and purification of nucleic acids, which directly impacts the quality of the sequencing results. Sequencing follows, where the actual genetic material is decoded using NGS technology. Data analysis and interpretation are vital stages in understanding complex genomic data, with bioinformatics tools playing a major role in identifying mutations and genetic markers associated with cancer. As the demand for personalized medicine increases, efficient workflow systems are essential for ensuring high-quality, actionable results.
The Application segment includes diagnostics, biomarker discovery, drug discovery, and others. NGS plays an essential role in cancer diagnostics by identifying genetic mutations and alterations that are specific to various cancer types. This allows for the development of personalized treatment plans, which can significantly improve patient outcomes. In biomarker discovery, NGS is used to identify genetic markers that help in early cancer detection and monitoring treatment responses. NGS also contributes to drug discovery by enabling researchers to understand the genetic basis of cancer, leading to the development of targeted therapies.
The End Use segment includes hospitals, diagnostic laboratories, academic and research institutions, and pharmaceutical and biotechnology companies. Hospitals are major users of NGS in clinical oncology, as they are equipped to conduct advanced genomic testing for cancer patients. Diagnostic laboratories also play a significant role in providing genetic testing services to aid in cancer diagnosis and treatment planning. Academic and research institutions are driving innovation in NGS technologies, while pharmaceutical and biotechnology companies use NGS in drug discovery and the development of new cancer therapies.
Finally, the Geography segmentation covers regions such as North America, Europe, Asia-Pacific, Latin America, and the Middle East & Africa. North America leads the market, driven by advanced healthcare infrastructure, high adoption of NGS technologies, and significant investments in cancer research. Europe follows closely, supported by strong healthcare systems and ongoing research in oncology. The Asia-Pacific region is experiencing rapid growth due to increasing healthcare access, rising cancer incidences, and advancements in biotechnology. Latin America and the Middle East & Africa are also emerging as key regions, with growing investments in healthcare and genomics.
Global Clinical Oncology Next Generation Sequencing Segment Analysis
In this report, the Global Clinical Oncology Next Generation Sequencing Market has been segmented by Technology, Workflow, Application, End Use, and Geography.
Global Clinical Oncology Next Generation Sequencing Market, Segmentation by Technology
The Global Clinical Oncology Next Generation Sequencing Market has been segmented by Technology into Whole Genome Sequencing, Whole Exome Sequencing and Targeted Sequencing & Resequencing.
Whole Genome Sequencing involves the comprehensive analysis of an individual's entire genome, providing a broad view of genetic variations across the genome, including both coding and non-coding regions. Whole Exome Sequencing focuses specifically on sequencing the protein-coding regions of the genome, known as the exome, which represent a small fraction of the total genome but contain a majority of disease-causing variants. Targeted Sequencing & Resequencing entail the selective sequencing of specific genomic regions or genes of interest, enabling high-throughput analysis of known mutations or biomarkers associated with cancer development, progression, and treatment response.
This segmentation framework reflects the diverse approaches and methodologies employed in clinical oncology NGS diagnostics, each offering unique advantages and applications in cancer research and patient care. Whole Genome Sequencing provides comprehensive genomic information but requires extensive data analysis and computational resources. Whole Exome Sequencing offers a cost-effective alternative for identifying disease-causing variants within protein-coding regions, while Targeted Sequencing & Resequencing enable focused analysis of specific genes or genomic regions relevant to cancer diagnosis, prognosis, and personalized treatment strategies. Understanding these distinct technologies is crucial for healthcare providers and researchers to leverage the full potential of NGS in advancing clinical oncology diagnostics and improving patient outcomes.
Global Clinical Oncology Next Generation Sequencing Market, Segmentation by Workflow
The Global Clinical Oncology Next Generation Sequencing Market has been segmented by Workflow into NGS Pre-Sequencing, NGS Sequencing and NGS Data Analysis.
NGS Pre-Sequencing involves sample preparation, library construction, and target enrichment, where genomic DNA or RNA from tumor samples is extracted, fragmented, and amplified to generate sequencing-ready libraries. This stage is crucial for ensuring high-quality input material and optimal sequencing performance. NGS Sequencing encompasses the actual process of DNA or RNA sequencing, where the prepared libraries are loaded onto NGS platforms for high-throughput sequencing, generating vast amounts of sequencing data. This step is characterized by the use of advanced sequencing technologies and instruments, such as Illumina, Ion Torrent, and PacBio platforms, to generate sequence reads with high accuracy and depth.
Following sequencing, NGS Data Analysis involves bioinformatics analysis, data interpretation, and variant calling, where the generated sequencing data is processed, aligned to the reference genome, and analyzed to identify genetic variants, somatic mutations, and other genomic alterations relevant to oncology. This stage requires specialized bioinformatics tools, algorithms, and expertise to accurately interpret sequencing data, annotate genomic variants, and correlate genetic findings with clinical relevance. Overall, the segmentation of the Global Clinical Oncology NGS Market by Workflow reflects the sequential steps involved in NGS-based oncology diagnostics, highlighting the importance of each stage in achieving accurate and actionable genomic insights for cancer diagnosis, prognosis, and treatment decision-making.
Global Clinical Oncology Next Generation Sequencing Market, Segmentation by Application
The Global Clinical Oncology Next Generation Sequencing Market has been segmented by Application into Screening, Companion Diagnostics and Others.
Screening involves the use of NGS technology for early detection and risk assessment of cancer, aiming to identify genetic mutations or biomarkers associated with increased cancer susceptibility. Companion Diagnostics refer to the use of NGS-based tests to guide personalized treatment decisions, such as identifying specific genetic alterations in tumors to predict response to targeted therapies or immunotherapies. This segment highlights the role of NGS in tailoring treatment strategies based on individual genetic profiles, improving treatment efficacy and patient outcomes. The "Others" category includes additional applications of NGS in clinical oncology, such as molecular profiling, tumor heterogeneity analysis, and minimal residual disease monitoring, showcasing the versatility and expanding utility of NGS technology in cancer research and clinical practice.
This segmentation framework provides a comprehensive view of the diverse applications of NGS in clinical oncology, emphasizing its role in various stages of cancer care, from early detection to treatment selection and monitoring. By focusing on these key applications, stakeholders can better understand the specific needs and challenges in different areas of clinical oncology, enabling the development of targeted NGS-based solutions and strategies to address these needs effectively. Additionally, this segmentation approach facilitates market analysis and forecasting, helping to identify emerging trends, opportunities, and growth drivers in the Global Clinical Oncology NGS Market.
Global Clinical Oncology Next Generation Sequencing Market, Segmentation by End Use
The Global Clinical Oncology Next Generation Sequencing Market has been segmented by End Use into Hospitals, Clinics, and Laboratories.
Hospitals are a key end user in the clinical mobility aids market, as these institutions often cater to patients with serious injuries, disabilities, or mobility challenges. Mobility aids such as wheelchairs, walkers, and crutches are essential in hospitals for both short-term recovery and long-term patient care. The need for these devices is amplified by the growing number of surgeries, particularly among the aging population, who require assistance with movement and mobility during their recovery. Hospitals also play a significant role in promoting rehabilitation programs that include the use of mobility aids.
Clinics represent another important end-use segment. In outpatient settings, clinics treat a large number of patients with varying degrees of mobility impairments, such as those recovering from minor surgeries or managing chronic conditions like arthritis. Mobility aids in clinics are essential for facilitating patient mobility, promoting independence, and aiding in rehabilitation processes. These facilities often provide a more accessible and affordable option for patients in need of mobility assistance, especially when hospital care is not required.
Laboratories also utilize mobility aids, especially those focused on patient rehabilitation, diagnostics, or physiotherapy. Laboratories within rehabilitation centers or research institutions use mobility devices to support clinical trials, studies on mobility impairments, and the development of new technologies to improve patient mobility. Though not as prominent as hospitals and clinics, the use of mobility aids in laboratories contributes to the advancement of assistive devices, particularly in terms of ergonomic designs and the integration of new technologies.
Global Clinical Oncology Next Generation Sequencing Market, Segmentation by Geography
In this report, the Global Clinical Oncology Next Generation Sequencing Market has been segmented by Geography into five regions; North America, Europe, Asia Pacific, Middle East and Africa and Latin America.
Global Clinical Oncology Next Generation Sequencing Market Share (%), by Geographical Region, 2024
North America, Europe, Asia Pacific, Middle East and Africa, and Latin America. Each region represents a unique market landscape with varying levels of adoption, regulatory frameworks, and healthcare infrastructure pertaining to clinical oncology NGS diagnostics. North America, comprising the United States and Canada, holds a prominent position in the global market, driven by advanced healthcare systems, robust research infrastructure, and high demand for personalized medicine. Europe is characterized by a strong emphasis on precision medicine initiatives and collaborations between academia, industry, and healthcare providers to advance oncology diagnostics and treatment. The Asia Pacific region, including countries such as China, Japan, and India, is witnessing rapid growth in clinical oncology NGS adoption, fueled by increasing cancer prevalence, rising healthcare expenditure, and expanding access to advanced molecular diagnostics.
In contrast, the Middle East and Africa region faces challenges such as limited access to healthcare services and resources, coupled with a high burden of cancer incidence, which presents opportunities for NGS-based oncology diagnostics to improve cancer care outcomes. Latin America represents a growing market for clinical oncology NGS, driven by improving healthcare infrastructure, rising investments in cancer research, and increasing awareness of personalized medicine approaches. By understanding the regional dynamics and market trends across these regions, stakeholders can identify growth opportunities, tailor their strategies, and navigate regulatory landscapes effectively to capitalize on the expanding Global Clinical Oncology NGS Market.
Market Trends
This report provides an in depth analysis of various factors that impact the dynamics of Global Clinical Oncology Next Generation Sequencing Market. These factors include; Market Drivers, Restraints and Opportunities Analysis.
Drivers, Restraints and Opportunity Analysis
Drivers :
- Rising Cancer Incidence
- Technological Advancements
-
Growing Awareness - The Global Clinical Oncology Next Generation Sequencing (NGS) Market is experiencing a surge in awareness driven by several factors. First and foremost, there is a growing recognition among healthcare professionals and researchers of the transformative potential of NGS technology in oncology diagnostics and treatment. As NGS becomes increasingly integrated into clinical practice, awareness of its capabilities and benefits is expanding, fueling adoption and investment in this field. Additionally, rising cancer incidence rates worldwide and the growing demand for personalized medicine are driving the need for more precise and comprehensive molecular profiling tools like NGS. Moreover, initiatives aimed at raising public awareness about cancer prevention, early detection, and precision oncology are further contributing to the increasing awareness of NGS technology and its role in advancing cancer care. As awareness continues to grow, particularly among patients, healthcare providers, and policymakers, the Global Clinical Oncology NGS Market is poised for significant expansion and innovation, paving the way for improved cancer diagnosis, treatment, and outcomes on a global scale.
Restraints :
- High Costs
- Data Analysis Challenges
-
Regulatory Issues - Regulatory issues play a pivotal role in shaping the landscape of the Global Clinical Oncology Next Generation Sequencing (NGS) Market. Due to the complex nature of NGS technology and its critical role in cancer diagnosis and treatment, regulatory agencies worldwide have implemented stringent guidelines and requirements to ensure the safety, efficacy, and quality of NGS-based tests. Key regulatory considerations include the approval process for NGS platforms and assays, the validation of NGS-based tests for clinical use, and the interpretation and reporting of genomic variants in oncology. Regulatory agencies such as the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) provide guidance and oversight to ensure compliance with regulatory standards, while also fostering innovation and advancement in NGS-based oncology diagnostics. Additionally, ongoing efforts to harmonize regulatory frameworks internationally aim to streamline the regulatory approval process and facilitate global market access for NGS-based tests, promoting interoperability and consistency in regulatory requirements across different regions.
Stakeholders in the Global Clinical Oncology NGS Market must navigate these regulatory challenges effectively to bring NGS-based tests to market, ensuring compliance with regulatory standards while also meeting the evolving needs of healthcare providers and patients. By proactively addressing regulatory requirements and collaborating with regulatory agencies, manufacturers and developers can accelerate the adoption of NGS technology in clinical oncology, driving progress towards personalized cancer care and improved patient outcomes.
Opportunity :
- Development of Liquid Biopsy Assays
- Increasing Investments
-
Rise of Personalized Medicine Platforms - The Global Clinical Oncology Next Generation Sequencing (NGS) Market is witnessing a significant rise in personalized medicine platforms, driven by the growing adoption of NGS technology and advancements in genomic profiling techniques. Personalized medicine platforms leverage NGS-based tests to analyze individual genetic profiles, tumor characteristics, and treatment responses, enabling tailored therapeutic approaches for cancer patients. These platforms integrate genomic data with clinical information to guide treatment decisions, identify targeted therapies or immunotherapies most likely to benefit patients, and predict treatment outcomes with greater precision. By harnessing the power of NGS technology, personalized medicine platforms empower oncologists to deliver more effective and personalized cancer care, improving patient outcomes and minimizing the risk of adverse reactions to treatments.
The emergence of personalized medicine platforms represents a paradigm shift in oncology diagnostics and treatment, offering unprecedented opportunities to revolutionize cancer care. By leveraging comprehensive genomic data and sophisticated bioinformatics algorithms, these platforms enable the development of personalized treatment strategies based on the unique molecular profiles of individual tumors. As personalized medicine continues to gain momentum in oncology, fueled by advances in NGS technology and growing evidence supporting its clinical utility, the Global Clinical Oncology NGS Market is poised for continued growth and innovation, driving the transformation of cancer care towards more precise, effective, and personalized approaches.
Competitive Landscape Analysis
Key players in Global Clinical Oncology Next Generation Sequencing Market include
- Illumina Inc
- F. Hoffmann-La Roche Ltd
- Agilent Technologies Inc
- Thermo Fisher Scientific
- Myriad Genetics Inc
- BGI
In this report, the profile of each market player provides following information:
- Company Overview and Product Portfolio
- Key Developments
- Financial Overview
- Strategies
- Company SWOT Analysis
- Introduction
- Research Objectives and Assumptions
- Research Methodology
- Abbreviations
- Market Definition & Study Scope
- Executive Summary
- Market Snapshot, By Technology
- Market Snapshot, By Workflow
- Market Snapshot, By Application
- Market Snapshot, By End Use
- Market Snapshot, By Region
- Global Clinical Oncology Next Generation Sequencing Market Dynamics
- Drivers, Restraints and Opportunities
- Drivers
- Rising Cancer Incidence
- Technological Advancements
- Growing Awareness
- Restraints
- High Costs
- Data Analysis Challenges
- Regulatory Issues
- Opportunities
- Development of Liquid Biopsy Assays
- Increasing Investments
- Rise of Personalized Medicine Platforms
- Drivers
- PEST Analysis
- Political Analysis
- Economic Analysis
- Social Analysis
- Technological Analysis
- Porter's Analysis
- Bargaining Power of Suppliers
- Bargaining Power of Buyers
- Threat of Substitutes
- Threat of New Entrants
-
Competitive Rivalry
- Drivers, Restraints and Opportunities
- Market Segmentation
- Global Clinical Oncology Next Generation Sequencing Market, By Technology, 2021- 2031 (USD Million)
- Whole Genome Sequencing
- Whole Exome Sequencing
- Targeted Sequencing & Resequencing
- Global Clinical Oncology Next Generation Sequencing Market, By Workflow, 2021 - 2031 (USD Million)
- NGS Pre-Sequencing
- NGS Sequencing
- NGS Data Analysis
- Global Clinical Oncology Next Generation Sequencing Market, By Application, 2021 - 2031 (USD Million)
- Screening
- Companion Diagnostics
- Others
- Global Clinical Oncology Next Generation Sequencing Market, By End Use, 2021 - 2031 (USD Million)
- Hospitals
- Clinics
- Laboratories
- Global Clinical Oncology Next Generation Sequencing Market, By Geography, 2021 - 2031 (USD Million)
- North America
- United States
- Canada
- Europe
- Germany
- United Kingdom
- France
- Italy
- Spain
- Nordic
- Benelux
- Rest of Europe
- Asia Pacific
- Japan
- China
- India
- Australia & New Zealand
- South Korea
- ASEAN (Association of South East Asian Countries)
- Rest of Asia Pacific
- Middle East & Africa
- GCC
- Israel
- South Africa
- Rest of Middle East & Africa
- Latin America
- Brazil
- Mexico
- Argentina
- Rest of Latin America
- North America
- Global Clinical Oncology Next Generation Sequencing Market, By Technology, 2021- 2031 (USD Million)
- Competitive Landscape
- Company Profiles
- Illumina Inc
- F. Hoffmann-La Roche Ltd
- Agilent Technologies Inc
- Thermo Fisher Scientific
- Myriad Genetics Inc
- BGI
- Company Profiles
- Analyst Views
- Future Outlook of the Market