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基因组癌症测试市场 - 全球产业规模、份额、趋势、机会和预测，按测试类型、技术、最终用户、地区和竞争细分，2019-2029F

Genomic Cancer Testing Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Test Type, By Technology, By End User, By Region and Competition, 2019-2029F
出版日期: | 出版商: TechSci Research | 英文 185 Pages | 商品交期: 2-3个工作天内

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简介目录

2023 年全球基因组癌症检测市值为 123.5 亿美元，预计在预测期内将稳定成长，到 2029 年复合年增长率为 9.42%。癌症患者的DNA 进行分析，以查明其基因中可能影响癌症进展的特定突变或变化。肿瘤学基因组测试的主要目标是识别可以为治疗决策提供资讯的基因改变。这使得肿瘤学家能够根据肿瘤独特的遗传特征选择更有可能有效的标靶治疗。此外，它还提供了有关癌症侵袭性及其对特定治疗的潜在反应的见解。此外，它还识别出可能表明其他类型癌症的风险升高的遗传性基因突变，从而指导监测和预防策略。

市场概况
预测期 2025-2029
2023 年市场规模 123.5亿美元
2029 年市场规模 209.7亿美元
2024-2029 年复合年增长率 9.42%
成长最快的细分市场 液体活检
最大的市场 北美洲

管理和解释大量基因组资料在储存、分析和确保资料安全方面提出了挑战。此外，与基因组测试和定序技术相关的高成本可能会限制可及性，特别是在欠发达地区。基因组定序技术的进步，例如下一代定序 (NGS)，透过对患者的基因组成进行全面分析，彻底改变了癌症诊断。这有助于精确识别与癌症相关的基因突变和变化。

液体活检技术涉及分析血液样本中的循环肿瘤 DNA (ctDNA) 或其他生物标记物，因其非侵入性以及监测治疗反应和检测癌症復发的能力而受到越来越多的重视。正在进行的生物标记研究、利用人工智慧 (AI) 进行资料分析以及与电子健康记录 (EHR) 的整合预计将推动该领域的创新。

全球基因组癌症检测领域代表了医疗保健领域一个充满活力且快速发展的领域，为在全球范围内推进癌症检测、提高治疗效果和改善患者治疗结果提供了前所未有的机会。

主要市场驱动因素

癌症发生率上升

政府措施和资助

主要市场挑战

测试成本

资料隐私和道德问题

主要市场趋势

技术进步

细分市场洞察

测试类型见解

技术洞察

区域洞察

目录

第 1 章：产品概述

第 2 章：研究方法

第 3 章：执行摘要

第 4 章：COVID-19 对全球基因组癌症检测市场的影响

第 5 章：全球基因组癌症检测市场展望

  • 市场规模及预测
    • 按价值
  • 市占率及预测
    • 依测试类型（基因组分析测试、液体活检测试、伴随诊断测试、药物基因组测试、遗传性癌症测试、其他）
    • 依技术（次世代定序 (NGS)、聚合酶连锁反应 (PCR)、萤光原位杂交 (FISH)、免疫组织化学 (IHC) 等）
    • 按最终使用者（医院、诊断实验室、学术和研究机构、癌症中心等）
    • 按地区
    • 按公司划分 (2023)
  • 市场地图

第 6 章：亚太地区基因组癌症检测市场展望

  • 市场规模及预测
    • 按价值
  • 市占率及预测
    • 按测试类型
    • 依技术
    • 按最终用户
    • 按国家/地区
  • 亚太地区：国家分析
    • 中国
    • 印度
    • 澳洲
    • 日本
    • 韩国

第 7 章：欧洲基因组癌症检测市场展望

  • 市场规模及预测
    • 按价值
  • 市占率及预测
    • 按测试类型
    • 依技术
    • 按最终用户
    • 按国家/地区
  • 欧洲：国家分析
    • 法国
    • 德国
    • 西班牙
    • 义大利
    • 英国

第 8 章：北美基因组癌症检测市场展望

  • 市场规模及预测
    • 按价值
  • 市占率及预测
    • 按测试类型
    • 依技术
    • 按最终用户
    • 按国家/地区
  • 北美：国家分析
    • 美国
    • 墨西哥
    • 加拿大

第 9 章：南美洲基因组癌症检测市场展望

  • 市场规模及预测
    • 按价值
  • 市占率及预测
    • 按测试类型
    • 依技术
    • 按最终用户
    • 按国家/地区
  • 南美洲：国家分析
    • 巴西
    • 阿根廷
    • 哥伦比亚

第 10 章：中东和非洲基因组癌症检测市场展望

  • 市场规模及预测
    • 按价值
  • 市占率及预测
    • 按测试类型
    • 依技术
    • 按最终用户
    • 按国家/地区
  • MEA：国家分析
    • 南非
    • 沙乌地阿拉伯
    • 阿联酋基因组癌症检测市场展望
      • 市场规模及预测
        • 按价值
      • 市占率及预测
        • 按测试类型
        • 依技术
        • 按最终用户

第 11 章：市场动态

  • 司机
  • 挑战

第 12 章：市场趋势与发展

  • 最近的发展
  • 产品发布
  • 併购

第 13 章：全球基因组癌症检测市场：SWOT 分析

第 14 章：波特的五力分析

  • 产业竞争
  • 新进入者的潜力
  • 供应商的力量
  • 客户的力量
  • 替代产品的威胁

第15章：竞争格局

  • Illumina, Inc.
  • F. Hoffmann-La Roche Ltd
  • QIAGEN NV
  • Merck KGaA
  • Abbott Laboratories Inc.
  • Novogene Co., Ltd.
  • Guardant Health, Inc.
  • Personal Genome Diagnostics Inc.
  • Thermo Fisher Scientific Inc.
  • NeoGenomics Laboratories, Inc.

第 16 章：策略建议

第17章调查会社について・免责事项

简介目录
Product Code: 24306

Global Genomic Cancer Testing Market was valued at USD 12.35 Billion in 2023 and is anticipated to project steady growth in the forecast period with a CAGR of 9.42% through 2029. Genomic cancer testing, also referred to as genetic testing or molecular profiling, entails the examination of a cancer patient's DNA to pinpoint specific mutations or changes in their genes that may be influencing the progression of their cancer. The primary objective of genomic testing in oncology is to identify genetic alterations that can inform treatment decisions. This enables oncologists to select targeted therapies that are more likely to be effective based on the unique genetic profile of the tumor. Moreover, it provides insights into the cancer's aggressiveness and its potential responsiveness to specific treatments. Additionally, it identifies inherited genetic mutations that could indicate an elevated risk of developing other types of cancer, thereby guiding strategies for monitoring and prevention.

Market Overview
Forecast Period2025-2029
Market Size 2023USD 12.35 Billion
Market Size 2029USD 20.97 Billion
CAGR 2024-20299.42%
Fastest Growing SegmentLiquid Biopsy
Largest MarketNorth America

Managing and interpreting extensive volumes of genomic data presents challenges in terms of storage, analysis, and ensuring data security. Furthermore, the high costs associated with genomic testing and sequencing technologies can restrict accessibility, particularly in less developed regions. Advances in genomic sequencing technologies, such as next-generation sequencing (NGS), have revolutionized cancer diagnostics by enabling comprehensive analysis of a patient's genetic composition. This facilitates precise identification of genetic mutations and alterations linked to cancer.

Liquid biopsy techniques, involving the analysis of circulating tumor DNA (ctDNA) or other biomarkers from blood samples, are increasingly valued for their non-invasive nature and ability to monitor treatment response and detect cancer recurrence. Ongoing research into biomarkers, utilization of artificial intelligence (AI) for data analysis, and integration with electronic health records (EHRs) are anticipated to fuel innovation in this field.

The global genomic cancer testing sector represents a dynamic and swiftly evolving segment within healthcare, offering unprecedented opportunities to advance cancer detection, enhance treatment effectiveness, and improve patient outcomes on a global scale.

Key Market Drivers

Rising Incidence of Cancer

The increasing global incidence of cancer underscores the urgent need for more effective diagnostic and treatment approaches, driving significant growth in the genomic cancer testing market. Genomic testing allows oncologists to identify specific genetic mutations and biomarkers associated with different types of cancer, enabling them to customize treatment plans tailored to each patient. According to a WHO report, it is projected that there will be over 35 million new cancer cases in 2050, marking a 77% increase from the estimated 20 million cases in 2022. This rise reflects both population aging, growth, and changes in exposure to risk factors associated with socioeconomic development.

This growing cancer burden, combined with increased adoption of genomic testing, has fueled substantial market expansion. Pharmaceutical companies, diagnostic laboratories, and healthcare providers are investing in genomic technologies and infrastructure to meet the growing demand for personalized cancer care. Genomic testing also plays a crucial role in early cancer detection and screening by analyzing genetic predispositions and mutations. This early detection often leads to more effective treatment options and improved survival rates.

Genomic data obtained through testing significantly contributes to ongoing clinical research and drug development efforts. Researchers utilize this data to better understand the genetic mechanisms of cancer, identify new drug targets, and develop more effective therapies. This continuous cycle of research and development drives innovation in oncology. As the number of targeted therapies and immunotherapies continues to grow, accurate genomic testing becomes increasingly essential for identifying suitable patients for these treatments.

Government Initiatives and Funding

Governments allocate funding to research institutions and universities to advance genomic technologies and their application in cancer research. This financial support accelerates innovation and the development of novel testing methods and biomarkers. For instance, in June 2024, the Australian Government committed over $27 million to eight new projects led by prominent researchers across the country. These initiatives aim to leverage genetic information for early disease detection, enhance cancer classification, and personalize treatment strategies for better patient outcomes. Among these projects, $8 million is dedicated to establishing a national platform for integrating AI technologies in diagnosing severe genetic disorders like muscular dystrophy. Additionally, nearly $8 million has been allocated to the Centre for Population Genomics, a collaboration between the Murdoch Children's Research Institute and the Garvan Institute of Medical Research.

Governments also implement public health programs that prioritize cancer screening and early detection, often incorporating genomic testing where feasible. These programs raise awareness and accessibility to genomic testing among the population, thereby stimulating market demand. In 2023, University of Melbourne researchers secured $2.4 million from the Medical Research Future Fund (MRFF) to investigate the potential of a new DNA test, administered through a straightforward saliva sample taken at a doctor's office, as a cost-effective and efficient method for assessing genetic susceptibility to specific cancers.

Government investment in healthcare infrastructure, including genomic sequencing facilities and laboratories, expands testing capacity and lowers costs, improving access for a broader patient base.In a similar initiative in 2024, Maharashtra Natural Gas Limited (MNGL) in India, through its CSR efforts, pledged support to the GeneHealth Lab at MUHS in Shivajinagar. This collaboration is expected to significantly enhance the institute's ability to provide sophisticated diagnostic services to economically disadvantaged communities.

Government initiatives and funding create an enabling environment for the growth of the global genomic cancer testing market by supporting research, establishing regulatory frameworks, promoting public health initiatives, investing in infrastructure, fostering industry collaboration, and promoting cost-effective healthcare solutions. These combined efforts drive advancements in genomic technologies and enhance cancer care on a global scale.

Key Market Challenges

Cost of Testing

The expense of genomic testing presents a substantial hurdle for the global market in genomic cancer testing. Establishing genomic testing facilities and procuring necessary equipment, such as sequencing machines and bioinformatics tools, demands significant initial investment. This upfront cost can pose a barrier for healthcare providers and laboratories aiming to provide genomic testing services. Although the cost of genomic sequencing technologies is decreasing over time, it remains relatively high in comparison to traditional diagnostic methods. The analysis of genomic data requires specialized bioinformatics expertise and substantial computational resources. Costs associated with data storage, processing, and analysis can be considerable, particularly for extensive genomic studies and population screening initiatives.

Reimbursement policies and coverage for genomic testing vary significantly across regions and healthcare systems. Insufficient reimbursement rates or a lack of coverage for genomic tests may dissuade healthcare providers from offering these services or limit patient access. Strategies to address these challenges include advancing technologies to reduce sequencing costs, developing cost-effective testing platforms, advocating for improved reimbursement policies, and promoting global initiatives aimed at ensuring fair access to genomic testing. These efforts are essential for enhancing affordability and expanding the utilization and impact of genomic testing in cancer care worldwide.

Data privacy and ethical concerns

Genomic testing generates highly sensitive information concerning individuals' genetic predispositions, including their potential risk for developing specific types of cancer. It is crucial to ensure the privacy and confidentiality of this data to maintain patient trust and comply with regulatory requirements. Concerns about genetic discrimination, such as the denial of insurance coverage or job opportunities based on genetic traits, can dissuade individuals from opting for genomic testing. Therefore, robust regulatory frameworks and policies are essential to protect individuals from such discrimination.

The security of genomic data is paramount due to its attractiveness to malicious actors. Safeguarding genomic databases and implementing strong measures against data breaches are critical to protect patient information and uphold data integrity. Ethical considerations arise regarding the use of genomic data for research, including obtaining informed consent, anonymizing data, and ensuring that data is used ethically and responsibly. Clear guidelines and ethical standards are necessary to govern the research use of genomic data and prevent unauthorized or inappropriate secondary uses.

Regulatory frameworks related to data privacy and genomic testing vary significantly across countries and regions, leading to challenges in establishing uniform standards for data protection and ethical use. To address these challenges, it is essential to develop comprehensive data protection measures, strengthen regulatory oversight, educate stakeholders about the benefits and ethical implications of genetic testing, and promote responsible practices in genomic research. These efforts are crucial for overcoming data privacy and ethical concerns in the global genomic cancer testing market and fostering trust among patients, healthcare providers, and researchers alike.

Key Market Trends

Technological advancements

Technological advancements have significantly reduced the cost of genomic sequencing, making genomic testing more accessible to healthcare providers and patients alike. Liquid biopsies, such as ctDNA testing, represent a breakthrough in cancer diagnostics as they analyze genetic material released by tumors into bodily fluids, providing real-time insights into cancer progression, treatment response, and the emergence of resistance mutations.

In 2023, ChromaCode highlighted advancements in their HDPCR NSCLC Assay, showcasing its advantages over Next Generation Sequencing (NGS) by delivering timely results and serving as a crucial backup option when NGS is not feasible. NGS technologies have also progressed, enabling rapid and comprehensive analysis of genomic data by simultaneously sequencing multiple genes or entire genomes, thereby enhancing the accuracy and depth of genetic information available for cancer patients.

AstraZeneca India partnered with the Rajiv Gandhi Cancer Institute and Research Center (RGCI) to establish a Center of Excellence (CoE) for lung cancer testing in Delhi. This collaboration aims to offer subsidized NGS molecular panel testing to eligible individuals diagnosed with lung cancer in India, improving treatment decisions based on validated genomic testing.

AI and machine learning are increasingly employed to interpret complex genomic data, identifying patterns, predicting outcomes, and enhancing diagnostic and treatment precision. Advances in miniaturization and point-of-care testing technologies are making genomic testing more accessible outside traditional laboratory settings, with portable sequencing devices and rapid diagnostic tools enabling timely decision-making in clinical settings.AI-driven risk profiling aids in early detection of common cancers like breast cancer, and AI can analyze X-rays to identify cancers in regions where imaging experts may be scarce. MIT's development of 'Sybil,' an AI model predicting lung cancer risk up to six years in advance using low-dose CT scans, demonstrates AI's capability in forecasting both short- and long-term cancer risks.

These technological advancements are accelerating genomic research and its applications in oncology, driving innovation, improving patient outcomes, and expanding the scope of personalized cancer care globally.

Segmental Insights

Test Type Insights

Based on Test Type, the Genomic Profiling tests emerged as the dominating segment in the global market for Genomic Cancer Testing in 2023. Genomic profiling tests conduct a thorough analysis of an individual's genetic composition, identifying mutations, variations, and cancer-associated biomarkers. This detailed genetic information allows healthcare providers to gain a precise understanding of the molecular drivers of cancer, enabling customized treatment strategies. Next-generation sequencing (NGS) technologies have significantly improved the capability and efficiency of genomic profiling tests. Exact Sciences Corp. has announced its intention to present new research supporting advancements in early cancer detection, genomic testing, and treatment guidance at the 2023 European Society for Medical Oncology (ESMO) Congress in Madrid, Spain. This includes trials evaluating their blood-based MCED program, OncoExTra data demonstrating the detection frequency of actionable fusions in nearly 8,000 people with solid tumors, which informs treatment decisions by assessing RNA and DNA through NGS.

Illumina, Inc. recently launched TruSight Oncology (TSO) Comprehensive (EU), a single test that evaluates multiple tumor genes and biomarkers to reveal the specific molecular profile of a patient's cancer. In a collaborative effort, Roche France and Foundation Medicine are transferring FoundationOne(R) Liquid CDx technology to the Institute Gustave Roussy in 2023. This initiative aims to offer comprehensive genomic profiling (CGP) through liquid biopsy testing to advanced cancer patients throughout France. Pharmaceutical companies and biotechnology firms are making substantial investments in genomic profiling technologies to advance targeted therapies and companion diagnostics. These collaborations foster innovation and expand the market for genomic testing, supporting advancements in precision medicine for cancer treatment.

Technology Insights

Based on Technology, the Next-Generation Sequencing emerged as the dominating segment in the global market for Genomic Cancer Testing in 2023. NGS enables the simultaneous sequencing of large portions or entire genomes, facilitating comprehensive analysis of genetic changes in cancer cells such as mutations, copy number variations, and structural alterations. This detailed information is critical for understanding cancer at a molecular level and tailoring personalized treatment strategies. The decreasing cost of NGS over time has enhanced its accessibility in routine clinical practice, leading to its widespread adoption across global healthcare settings.

In 2024, Lt Gen Daljit Singh, Director General of Armed Forces Medical Services and Senior Colonel Commandant of the Army Medical Corps, inaugurated the new Genome Sequencing Lab at the Armed Forces Medical College (AFMC) in Pune. This state-of-the-art facility features advanced Next Generation Sequencing (NGS) technologies, including "Nextseq 2000" and "Miniseq" analyzers, supporting continuous advancements in NGS technology, bioinformatics tools, and data analysis techniques. These capabilities empower researchers and clinicians to explore complex genomic landscapes more effectively, unlocking new insights into cancer biology and treatment strategies.In 2024, OGT, a leading global provider of genomic research and diagnostic solutions, introduced the RNA-based SureSeq Myeloid Fusion Panel. This next-generation sequencing (NGS) tool is designed to identify crucial fusion genes associated with acute myeloid leukemia (AML), further exemplifying the ongoing advancements and applications of NGS in oncology research and clinical diagnostics.

Regional Insights

Based on Region, North America emerged as the dominant region in the Global Genomic Cancer Testing Market in 2023. North America's healthcare infrastructure is distinguished by advanced medical technology, and extensive network of research institutions and universities. This robust framework not only supports pioneering research but also facilitates the adoption of cutting-edge diagnostic technologies like Next-Generation Sequencing (NGS). The region benefits significantly from the presence of leading pharmaceutical companies, biotechnology firms, and academic research centers, which collectively foster an environment conducive to continuous innovation. Regulatory oversight, exemplified by agencies such as the FDA in the United States, ensures rigorous standards for healthcare products and technologies, enhancing confidence in their safety and efficacy. In 2024, Thermo Fisher Scientific Inc. collaborated with the National Cancer Institute (NCI) on the myeloMATCH (Molecular Analysis for Therapy Choice) precision medicine trial. This initiative utilizes Thermo Fisher's NGS technology to analyze genetic biomarkers in patients' bone marrow and blood, aiming to streamline patient enrollment in clinical trials by matching them more efficiently with treatments targeting specific mutations identified in their samples. ongoing developments such as Helio Genomics exploring new AI-driven diagnostic opportunities and Datar Cancer Genetics seeking to introduce a circulating glial cell assay for brain cancer diagnosis highlight North America's leadership in genomic cancer testing and healthcare innovation. These advancements underscore the region's pivotal role in advancing personalized medicine and precision oncology globally.

Key Market Players

Illumina, Inc.

F. Hoffmann-La Roche Ltd

QIAGEN NV

Merck KGaA

Abbott Laboratories Inc.

Novogene Co., Ltd.

Guardant Health, Inc.

Personal Genome Diagnostics Inc.

Thermo Fisher Scientific Inc.

NeoGenomics Laboratories, Inc.

Report Scope:

In this report, the Global Genomic Cancer Testing Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:

Genomic Cancer Testing Market, By Test Type:

    Genomic Profiling Tests Liquid Biopsy Tests Companion Diagnostic Tests Pharmacogenomic Tests Hereditary Cancer Tests Others

Genomic Cancer Testing Market, By Technology:

    Next-Generation Sequencing (NGS) Polymerase Chain Reaction (PCR) Fluorescence In Situ Hybridization (FISH) Immunohistochemistry (IHC) Others

Genomic Cancer Testing Market, By End User:

    Hospitals Diagnostic Laboratories Academic and Research Institutions Cancer Centers Others

Genomic Cancer Testing Market, By Region:

    North America
    • United States
    • Canada
    • Mexico
    Europe
    • France
    • United Kingdom
    • Italy
    • Germany
    • Spain
    Asia Pacific
    • China
    • India
    • Japan
    • Australia
    • South Korea
    South America
    • Brazil
    • Argentina
    • Colombia
    Middle East & Africa
    • South Africa
    • Saudi Arabia
    • UAE

Competitive Landscape

Company Profiles: Detailed analysis of the major companies presents in the Global Genomic Cancer Testing Market.

Available Customizations:

Global Genomic Cancer Testing Market report with the given market data, Tech Sci Research offers customizations according to a company's specific needs. The following customization options are available for the report:

Company Information

Detailed analysis and profiling of additional market players (up to five).

Table of Contents

1. Product Overview

  • 1.1. Market Definition
  • 1.2. Scope of the Market
    • 1.2.1. Markets Covered
    • 1.2.2. Years Considered for Study
    • 1.2.3. Key Market Segmentations

2. Research Methodology

  • 2.1. Objective of the Study
  • 2.2. Baseline Methodology
  • 2.3. Key Industry Partners
  • 2.4. Major Association and Secondary Sources
  • 2.5. Forecasting Methodology
  • 2.6. Data Triangulation & Validation
  • 2.7. Assumptions and Limitations

3. Executive Summary

  • 3.1. Overview of the Market
  • 3.2. Overview of Key Market Segmentations
  • 3.3. Overview of Key Market Players
  • 3.4. Overview of Key Regions/Countries
  • 3.5. Overview of Market Drivers, Challenges, Trends

4. Impact of COVID-19 on Global Genomic Cancer Testing Market

5. Global Genomic Cancer Testing Market Outlook

  • 5.1. Market Size & Forecast
    • 5.1.1. By Value
  • 5.2. Market Share & Forecast
    • 5.2.1. By Test Type (Genomic Profiling Tests, Liquid Biopsy Tests, Companion Diagnostic Tests, Pharmacogenomic Tests, Hereditary Cancer Tests, Others)
    • 5.2.2. By Technology (Next-Generation Sequencing (NGS), Polymerase Chain Reaction (PCR), Fluorescence In Situ Hybridization (FISH), Immunohistochemistry (IHC), Others)
    • 5.2.3. By End User (Hospitals, Diagnostic Laboratories, Academic and Research Institutions, Cancer Centers, Others)
    • 5.2.4. By Region
    • 5.2.5. By Company (2023)
  • 5.3. Market Map

6. Asia Pacific Genomic Cancer Testing Market Outlook

  • 6.1. Market Size & Forecast
    • 6.1.1. By Value
  • 6.2. Market Share & Forecast
    • 6.2.1. By Test Type
    • 6.2.2. By Technology
    • 6.2.3. By End User
    • 6.2.4. By Country
  • 6.3. Asia Pacific: Country Analysis
    • 6.3.1. China Genomic Cancer Testing Market Outlook
      • 6.3.1.1. Market Size & Forecast
        • 6.3.1.1.1. By Value
      • 6.3.1.2. Market Share & Forecast
        • 6.3.1.2.1. By Test Type
        • 6.3.1.2.2. By Technology
        • 6.3.1.2.3. By End User
    • 6.3.2. India Genomic Cancer Testing Market Outlook
      • 6.3.2.1. Market Size & Forecast
        • 6.3.2.1.1. By Value
      • 6.3.2.2. Market Share & Forecast
        • 6.3.2.2.1. By Test Type
        • 6.3.2.2.2. By Technology
        • 6.3.2.2.3. By End User
    • 6.3.3. Australia Genomic Cancer Testing Market Outlook
      • 6.3.3.1. Market Size & Forecast
        • 6.3.3.1.1. By Value
      • 6.3.3.2. Market Share & Forecast
        • 6.3.3.2.1. By Test Type
        • 6.3.3.2.2. By Technology
        • 6.3.3.2.3. By End User
    • 6.3.4. Japan Genomic Cancer Testing Market Outlook
      • 6.3.4.1. Market Size & Forecast
        • 6.3.4.1.1. By Value
      • 6.3.4.2. Market Share & Forecast
        • 6.3.4.2.1. By Test Type
        • 6.3.4.2.2. By Technology
        • 6.3.4.2.3. By End User
    • 6.3.5. South Korea Genomic Cancer Testing Market Outlook
      • 6.3.5.1. Market Size & Forecast
        • 6.3.5.1.1. By Value
      • 6.3.5.2. Market Share & Forecast
        • 6.3.5.2.1. By Test Type
        • 6.3.5.2.2. By Technology
        • 6.3.5.2.3. By End User

7. Europe Genomic Cancer Testing Market Outlook

  • 7.1. Market Size & Forecast
    • 7.1.1. By Value
  • 7.2. Market Share & Forecast
    • 7.2.1. By Test Type
    • 7.2.2. By Technology
    • 7.2.3. By End User
    • 7.2.4. By Country
  • 7.3. Europe: Country Analysis
    • 7.3.1. France Genomic Cancer Testing Market Outlook
      • 7.3.1.1. Market Size & Forecast
        • 7.3.1.1.1. By Value
      • 7.3.1.2. Market Share & Forecast
        • 7.3.1.2.1. By Test Type
        • 7.3.1.2.2. By Technology
        • 7.3.1.2.3. By End User
    • 7.3.2. Germany Genomic Cancer Testing Market Outlook
      • 7.3.2.1. Market Size & Forecast
        • 7.3.2.1.1. By Value
      • 7.3.2.2. Market Share & Forecast
        • 7.3.2.2.1. By Test Type
        • 7.3.2.2.2. By Technology
        • 7.3.2.2.3. By End User
    • 7.3.3. Spain Genomic Cancer Testing Market Outlook
      • 7.3.3.1. Market Size & Forecast
        • 7.3.3.1.1. By Value
      • 7.3.3.2. Market Share & Forecast
        • 7.3.3.2.1. By Test Type
        • 7.3.3.2.2. By Technology
        • 7.3.3.2.3. By End User
    • 7.3.4. Italy Genomic Cancer Testing Market Outlook
      • 7.3.4.1. Market Size & Forecast
        • 7.3.4.1.1. By Value
      • 7.3.4.2. Market Share & Forecast
        • 7.3.4.2.1. By Test Type
        • 7.3.4.2.2. By Technology
        • 7.3.4.2.3. By End User
    • 7.3.5. United Kingdom Genomic Cancer Testing Market Outlook
      • 7.3.5.1. Market Size & Forecast
        • 7.3.5.1.1. By Value
      • 7.3.5.2. Market Share & Forecast
        • 7.3.5.2.1. By Test Type
        • 7.3.5.2.2. By Technology
        • 7.3.5.2.3. By End User

8. North America Genomic Cancer Testing Market Outlook

  • 8.1. Market Size & Forecast
    • 8.1.1. By Value
  • 8.2. Market Share & Forecast
    • 8.2.1. By Test Type
    • 8.2.2. By Technology
    • 8.2.3. By End User
    • 8.2.4. By Country
  • 8.3. North America: Country Analysis
    • 8.3.1. United States Genomic Cancer Testing Market Outlook
      • 8.3.1.1. Market Size & Forecast
        • 8.3.1.1.1. By Value
      • 8.3.1.2. Market Share & Forecast
        • 8.3.1.2.1. By Test Type
        • 8.3.1.2.2. By Technology
        • 8.3.1.2.3. By End User
    • 8.3.2. Mexico Genomic Cancer Testing Market Outlook
      • 8.3.2.1. Market Size & Forecast
        • 8.3.2.1.1. By Value
      • 8.3.2.2. Market Share & Forecast
        • 8.3.2.2.1. By Test Type
        • 8.3.2.2.2. By Technology
        • 8.3.2.2.3. By End User
    • 8.3.3. Canada Genomic Cancer Testing Market Outlook
      • 8.3.3.1. Market Size & Forecast
        • 8.3.3.1.1. By Value
      • 8.3.3.2. Market Share & Forecast
        • 8.3.3.2.1. By Test Type
        • 8.3.3.2.2. By Technology
        • 8.3.3.2.3. By End User

9. South America Genomic Cancer Testing Market Outlook

  • 9.1. Market Size & Forecast
    • 9.1.1. By Value
  • 9.2. Market Share & Forecast
    • 9.2.1. By Test Type
    • 9.2.2. By Technology
    • 9.2.3. By End User
    • 9.2.4. By Country
  • 9.3. South America: Country Analysis
    • 9.3.1. Brazil Genomic Cancer Testing Market Outlook
      • 9.3.1.1. Market Size & Forecast
        • 9.3.1.1.1. By Value
      • 9.3.1.2. Market Share & Forecast
        • 9.3.1.2.1. By Test Type
        • 9.3.1.2.2. By Technology
        • 9.3.1.2.3. By End User
    • 9.3.2. Argentina Genomic Cancer Testing Market Outlook
      • 9.3.2.1. Market Size & Forecast
        • 9.3.2.1.1. By Value
      • 9.3.2.2. Market Share & Forecast
        • 9.3.2.2.1. By Test Type
        • 9.3.2.2.2. By Technology
        • 9.3.2.2.3. By End User
    • 9.3.3. Colombia Genomic Cancer Testing Market Outlook
      • 9.3.3.1. Market Size & Forecast
        • 9.3.3.1.1. By Value
      • 9.3.3.2. Market Share & Forecast
        • 9.3.3.2.1. By Test Type
        • 9.3.3.2.2. By Technology
        • 9.3.3.2.3. By End User

10. Middle East and Africa Genomic Cancer Testing Market Outlook

  • 10.1. Market Size & Forecast
    • 10.1.1. By Value
  • 10.2. Market Share & Forecast
    • 10.2.1. By Test Type
    • 10.2.2. By Technology
    • 10.2.3. By End User
    • 10.2.4. By Country
  • 10.3. MEA: Country Analysis
    • 10.3.1. South Africa Genomic Cancer Testing Market Outlook
      • 10.3.1.1. Market Size & Forecast
        • 10.3.1.1.1. By Value
      • 10.3.1.2. Market Share & Forecast
        • 10.3.1.2.1. By Test Type
        • 10.3.1.2.2. By Technology
        • 10.3.1.2.3. By End User
    • 10.3.2. Saudi Arabia Genomic Cancer Testing Market Outlook
        • 10.3.2.1.1. By Value
      • 10.3.2.2. Market Share & Forecast
        • 10.3.2.2.1. By Test Type
        • 10.3.2.2.2. By Technology
        • 10.3.2.2.3. By End User
    • 10.3.3. UAE Genomic Cancer Testing Market Outlook
      • 10.3.3.1. Market Size & Forecast
        • 10.3.3.1.1. By Value
      • 10.3.3.2. Market Share & Forecast
        • 10.3.3.2.1. By Test Type
        • 10.3.3.2.2. By Technology
        • 10.3.3.2.3. By End User

11. Market Dynamics

  • 11.1. Drivers
  • 11.2. Challenges

12. Market Trends & Developments

  • 12.1. Recent Developments
  • 12.2. Product Launches
  • 12.3. Mergers & Acquisitions

13. Global Genomic Cancer Testing Market: SWOT Analysis

14. Porter's Five Forces Analysis

  • 14.1. Competition in the Industry
  • 14.2. Potential of New Entrants
  • 14.3. Power of Suppliers
  • 14.4. Power of Customers
  • 14.5. Threat of Substitute Product

15. Competitive Landscape

  • 15.1. Illumina, Inc.
    • 15.1.1. Business Overview
    • 15.1.2. Company Snapshot
    • 15.1.3. Products & Services
    • 15.1.4. Financials (As Reported)
    • 15.1.5. Recent Developments
  • 15.2. F. Hoffmann-La Roche Ltd
  • 15.3. QIAGEN NV
  • 15.4. Merck KGaA
  • 15.5. Abbott Laboratories Inc.
  • 15.6. Novogene Co., Ltd.
  • 15.7. Guardant Health, Inc.
  • 15.8. Personal Genome Diagnostics Inc.
  • 15.9. Thermo Fisher Scientific Inc.
  • 15.10. NeoGenomics Laboratories, Inc.

16. Strategic Recommendations

17. About Us & Disclaimer