세계의 맞춤형 유전체 의학 시장 예측(-2032년) : 제품별, 제공 형태별, 기술별, 용도별, 최종사용자별, 지역별 분석

According to Stratistics MRC, the Global Personalized Genomic Medicine Market is accounted for $663.9 billion in 2025 and is expected to reach $1,145.2 billion by 2032 growing at a CAGR of 8.1% during the forecast period. Personalized genomic medicine is a cutting-edge approach to healthcare that tailors medical treatment and prevention strategies to an individual's genetic makeup. By analyzing a person's DNA, clinicians can identify genetic variations that influence disease risk, drug response, and treatment efficacy. This enables more accurate diagnoses, targeted therapies, and proactive health management. It is especially impactful in oncology, rare genetic disorders, and pharmacogenomics. As genomic sequencing becomes more accessible and data integration improves, personalized genomic medicine is transforming traditional care models into more precise, predictive, and patient-centered systems, enhancing outcomes and reducing trial-and-error in clinical decision-making.

Market Dynamics:

Driver:

Advancements in Genomic Sequencing Technologies

Advancements in genomic sequencing technologies are a key driver of the personalized genomic medicine market. Innovations in next-generation sequencing (NGS) have made genetic analysis faster, more accurate, and cost-effective. These improvements enable clinicians to identify disease-causing mutations and tailor treatments accordingly. As sequencing becomes more accessible, its integration into routine clinical workflows is expanding. The ability to decode complex genetic data with precision is revolutionizing diagnostics, drug development, and preventive care, fueling growth across healthcare and research sectors.

Restraint:

High Cost of Genomic Testing

High costs associated with genomic testing remain a major restraint in the personalized genomic medicine market. Despite technological progress, comprehensive DNA sequencing and analysis require expensive equipment, skilled personnel, and complex data interpretation. These financial barriers limit access, especially in low- and middle-income regions. Insurance coverage and reimbursement policies are often inconsistent, further restricting adoption. Until cost-effective solutions and broader affordability are achieved, the full potential of personalized genomic medicine may remain out of reach for many populations.

Opportunity:

Rising Demand for Precision Medicine

The rising demand for precision medicine presents a significant opportunity for the market. Patients and healthcare providers increasingly seek tailored treatments that consider genetic, environmental, and lifestyle factors. Genomic insights enable targeted therapies, reduce adverse drug reactions, and improve clinical outcomes. This shift toward individualized care is especially impactful in oncology, rare diseases, and pharmacogenomics. As awareness grows and technology advances, precision medicine is becoming a cornerstone of modern healthcare, driving investment and innovation in genomic solutions.

Threat:

Regulatory Challenges

Regulatory challenges pose a threat to the growth of the personalized genomic medicine market. The complexity of genetic data, ethical considerations, and varying global standards create hurdles in clinical implementation and commercialization. Approval processes for genomic tests and therapies can be slow and inconsistent, delaying access to innovative solutions. Data privacy laws and consent frameworks also vary widely, complicating cross-border research and patient engagement. Addressing these regulatory issues is essential to ensure safe, equitable, and scalable adoption of genomic medicine.

Covid-19 Impact:

The COVID-19 pandemic accelerated interest in personalized genomic medicine by highlighting the importance of genetic factors in disease susceptibility and treatment response. Genomic tools were used to study virus-host interactions, develop targeted therapies, and understand vaccine efficacy. The crisis underscored the need for rapid, data-driven healthcare solutions, boosting investment in genomic research and infrastructure. Post-pandemic, healthcare systems are increasingly integrating personalized approaches to improve resilience and patient outcomes. This shift is expected to sustain long-term growth in the genomic medicine market.

The bioinformatics segment is expected to be the largest during the forecast period

The bioinformatics segment is expected to account for the largest market share during the forecast period, due to its critical role in managing and interpreting complex genomic data. Bioinformatics tools enable efficient analysis of DNA sequences, identification of disease markers, and prediction of treatment responses. As genomic datasets grow exponentially, advanced algorithms and software platforms are essential for clinical decision-making. The integration of bioinformatics into diagnostics, drug development, and personalized care is expanding rapidly, making it a foundational component of genomic medicine.

The neurology segment is expected to have the highest CAGR during the forecast period

Over the forecast period, the neurology segment is predicted to witness the highest growth rate, due to increasing research into genetic factors underlying neurological disorders. Conditions such as Alzheimer's, Parkinson's, and epilepsy are being studied through genomic profiling to develop targeted therapies and early diagnostic tools. Personalized approaches in neurology offer hope for improved treatment outcomes and reduced disease progression. As awareness and funding grow, genomic medicine is becoming central to neurological care, driving rapid expansion and innovation in this segment.

Region with largest share:

During the forecast period, the Asia Pacific region is expected to hold the largest market share, due to rising healthcare investments, expanding genomics research, and growing demand for precision medicine. Countries like China, India, and Japan are advancing genomic infrastructure and launching national initiatives to integrate personalized care. The region's large population base, increasing chronic disease burden, and improving digital health capabilities contribute to strong market potential. Asia Pacific continues to lead in adoption and innovation across genomic applications.

Region with highest CAGR:

Over the forecast period, the North America region is anticipated to exhibit the highest CAGR, owing to robust research infrastructure, favorable regulatory frameworks, and high healthcare spending. The region is home to leading genomic companies, academic institutions, and clinical trial networks. Strong demand for precision therapies, widespread use of NGS, and supportive reimbursement policies further accelerate growth. As personalized medicine becomes mainstream, North America remains at the forefront of genomic innovation, shaping global trends and standards.

Key players in the market

Some of the key players in Personalized Genomic Medicine Market include Roche, Illumina, Thermo Fisher Scientific, Pfizer, Novartis, Qiagen, Foundation Medicine, GE Healthcare, Myriad Genetics, AstraZeneca, Exact Sciences, 23andMe, Biogen, IBM Watson Health, and Decode Genetics.

Key Developments:

In May 2025, Pfizer has entered into an exclusive global licensing agreement with 3SBio for SSGJ-707, a bispecific antibody targeting PD-1 and VEGF. This promising cancer therapy is undergoing clinical trials in China for non-small cell lung cancer, metastatic colorectal cancer, and gynecological tumors. Under the agreement, Pfizer will pay 3SBio an upfront fee of $1.25 billion, with potential milestone payments up to $4.8 billion, and tiered royalties on sales.

In February 2025, Alloy Therapeutics and Pfizer have entered into a strategic collaboration to develop a novel antibody discovery platform aimed at targeting complex disease mechanisms. Leveraging Alloy's innovative technologies, the partnership seeks to enhance the development of effective antibody-based therapies.

Products Covered:

• Diagnostics
• Therapeutics
• Preventive Medicine
• Genomic Data Interpretation Tools
• Other Products

Mode of Deliveries Covered:

• In-House Services
• Outsourced Services

Technologies Covered:

• Next-Generation Sequencing (NGS)
• Polymerase Chain Reaction (PCR)
• Microarray
• Gene Editing (CRISPR/Cas9)
• Bioinformatics
• Other Technologies

Applications Covered:

• Oncology
• Cardiovascular Diseases
• Neurology
• Infectious Diseases
• Rare Genetic Disorders
• Pharmacogenomics
• Other Applications

End Users Covered:

• Hospitals and Clinics
• Diagnostic Laboratories
• Academic and Research Institutes
• Pharmaceutical and Biotechnology Companies
• Other End Users

Regions Covered:

• North America
  • US
  • Canada
  • Mexico
• Europe
  • Germany
  • UK
  • Italy
  • France
  • Spain
  • Rest of Europe
• Asia Pacific
  • Japan
  • China
  • India
  • Australia
  • New Zealand
  • South Korea
  • Rest of Asia Pacific
• South America
  • Argentina
  • Brazil
  • Chile
  • Rest of South America
• Middle East & Africa
  • Saudi Arabia
  • UAE
  • Qatar
  • South Africa
  • Rest of Middle East & Africa

What our report offers:

• Market share assessments for the regional and country-level segments
• Strategic recommendations for the new entrants
• Covers Market data for the years 2024, 2025, 2026, 2028, and 2032
• Market Trends (Drivers, Constraints, Opportunities, Threats, Challenges, Investment Opportunities, and recommendations)
• Strategic recommendations in key business segments based on the market estimations
• Competitive landscaping mapping the key common trends
• Company profiling with detailed strategies, financials, and recent developments
• Supply chain trends mapping the latest technological advancements

Free Customization Offerings:

All the customers of this report will be entitled to receive one of the following free customization options:

• Company Profiling
  • Comprehensive profiling of additional market players (up to 3)
  • SWOT Analysis of key players (up to 3)
• Regional Segmentation
  • Market estimations, Forecasts and CAGR of any prominent country as per the client's interest (Note: Depends on feasibility check)
• Competitive Benchmarking
  • Benchmarking of key players based on product portfolio, geographical presence, and strategic alliances

Table of Contents

1 Executive Summary

2 Preface

• 2.1 Abstract
• 2.2 Stake Holders
• 2.3 Research Scope
• 2.4 Research Methodology
  • 2.4.1 Data Mining
  • 2.4.2 Data Analysis
  • 2.4.3 Data Validation
  • 2.4.4 Research Approach
• 2.5 Research Sources
  • 2.5.1 Primary Research Sources
  • 2.5.2 Secondary Research Sources
  • 2.5.3 Assumptions

3 Market Trend Analysis

• 3.1 Introduction
• 3.2 Drivers
• 3.3 Restraints
• 3.4 Opportunities
• 3.5 Threats
• 3.6 Product Analysis
• 3.7 Technology Analysis
• 3.8 Application Analysis
• 3.9 End User Analysis
• 3.10 Emerging Markets
• 3.11 Impact of Covid-19

4 Porters Five Force Analysis

• 4.1 Bargaining power of suppliers
• 4.2 Bargaining power of buyers
• 4.3 Threat of substitutes
• 4.4 Threat of new entrants
• 4.5 Competitive rivalry

5 Global Personalized Genomic Medicine Market, By Product

• 5.1 Introduction
• 5.2 Diagnostics
• 5.3 Therapeutics
• 5.4 Preventive Medicine
• 5.5 Genomic Data Interpretation Tools
• 5.6 Other Products

6 Global Personalized Genomic Medicine Market, By Mode of Delivery

• 6.1 Introduction
• 6.2 In-House Services
• 6.3 Outsourced Services

7 Global Personalized Genomic Medicine Market, By Technology

• 7.1 Introduction
• 7.2 Next-Generation Sequencing (NGS)
• 7.3 Polymerase Chain Reaction (PCR)
• 7.4 Microarray
• 7.5 Gene Editing (CRISPR/Cas9)
• 7.6 Bioinformatics
• 7.7 Other Technologies

8 Global Personalized Genomic Medicine Market, By Application

• 8.1 Introduction
• 8.2 Oncology
• 8.3 Cardiovascular Diseases
• 8.4 Neurology
• 8.5 Infectious Diseases
• 8.6 Rare Genetic Disorders
• 8.7 Pharmacogenomics
• 8.8 Other Applications

9 Global Personalized Genomic Medicine Market, By End User

• 9.1 Introduction
• 9.2 Hospitals and Clinics
• 9.3 Diagnostic Laboratories
• 9.4 Academic and Research Institutes
• 9.5 Pharmaceutical and Biotechnology Companies
• 9.6 Other End Users

10 Global Personalized Genomic Medicine Market, By Geography

• 10.1 Introduction
• 10.2 North America
  • 10.2.1 US
  • 10.2.2 Canada
  • 10.2.3 Mexico
• 10.3 Europe
  • 10.3.1 Germany
  • 10.3.2 UK
  • 10.3.3 Italy
  • 10.3.4 France
  • 10.3.5 Spain
  • 10.3.6 Rest of Europe
• 10.4 Asia Pacific
  • 10.4.1 Japan
  • 10.4.2 China
  • 10.4.3 India
  • 10.4.4 Australia
  • 10.4.5 New Zealand
  • 10.4.6 South Korea
  • 10.4.7 Rest of Asia Pacific
• 10.5 South America
  • 10.5.1 Argentina
  • 10.5.2 Brazil
  • 10.5.3 Chile
  • 10.5.4 Rest of South America
• 10.6 Middle East & Africa
  • 10.6.1 Saudi Arabia
  • 10.6.2 UAE
  • 10.6.3 Qatar
  • 10.6.4 South Africa
  • 10.6.5 Rest of Middle East & Africa

11 Key Developments

• 11.1 Agreements, Partnerships, Collaborations and Joint Ventures
• 11.2 Acquisitions & Mergers
• 11.3 New Product Launch
• 11.4 Expansions
• 11.5 Other Key Strategies

12 Company Profiling

• 12.1 Roche
• 12.2 Illumina
• 12.3 Thermo Fisher Scientific
• 12.4 Pfizer
• 12.5 Novartis
• 12.6 Qiagen
• 12.7 Foundation Medicine
• 12.8 GE Healthcare
• 12.9 Myriad Genetics
• 12.10 AstraZeneca
• 12.11 Exact Sciences
• 12.12 23andMe
• 12.13 Biogen
• 12.14 IBM Watson Health
• 12.15 Decode Genetics