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시장보고서
상품코드
1558611
세계의 전게놈 및 엑솜 시퀀싱 시장 : 제품별, 워크플로우별, 용도별, 최종사용자별, 지역별, 경쟁 구도 - 분석과 예측(2024-2033년)Global Whole Genome and Exome Sequencing Market: Focus on Product, Workflow, Application, End User, Region, and Competitive Landscape - Analysis and Forecast, 2024-2033 |
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전게놈 시퀀스(WGS) 및 엑솜 시퀀스(WES)는 생물 유전 물질의 종합적 해석을 가능하게 하는 최첨단 게놈 기술입니다.
WGS는 코드 영역과 비코드 영역을 모두 포함하는 전체 유전체을 시퀀싱하여 완전한 유전자 설계도를 제공합니다. 반면, WES는 엑손 영역(유전체의 단백질을 암호화하는 부분, 유전체의 약 1-2%를 차지하지만 알려진 질병과 관련된 변이체의 대부분을 포함하는 부분)만을 시퀀싱하는 데 중점을 둡니다. 이러한 기술은 유전적 변이, 질병 메커니즘, 진화 생물학에 대한 전례 없는 인사이트을 제공함으로써 유전체학에 혁명을 일으켰습니다. 임상 진단, 맞춤형 의료, 종양학, 희귀질환 연구 등 다양한 분야에 적용되어 의료 및 생물 의학 연구를 크게 발전시키고 있습니다. 지속적인 기술 개선, 비용 절감, 용도 확대로 WGS와 WES는 현대 유전체학에서 필수적인 툴로 자리 잡고 있습니다.
| 주요 시장 통계 | |
|---|---|
| 예측 기간 | 2024-2033년 |
| 2024년 평가 | 21억 120만 달러 |
| 2033년 예측 | 74억 6,760만 달러 |
| CAGR | 15.13% |
세계의 전게놈 및 엑솜 시퀀싱 시장 규모는 2023년에 18억 7,380만 달러에 달했습니다. 이 시장은 2033년에는 74억 6,760만 달러에 달할 것으로 예측되며, 15.13%라는 현저한 CAGR을 기록하며, 대폭적인 성장이 전망되고 있습니다. 이러한 급격한 증가는 맞춤형 의료에 대한 수요 증가와 전 세계 유전성 질환의 유병률 증가를 반영하고 있습니다. 정밀의료의 핵심 요소인 유전자 검사는 개인이 다양한 질병에 대한 유전적 소인을 평가할 수 있게 함으로써 환자와 의료진에게 예방적 개입과 맞춤형 치료 전략에 대한 귀중한 인사이트을 제공합니다. 기술의 발전으로 유전자 검사의 정확성과 접근성이 지속적으로 향상됨에 따라 이 시장은 의료 서비스 제공에 혁명을 일으키며 전 세계에서 예방 및 맞춤 의료의 시대를 열어가고 있습니다.
전게놈 및 엑솜 시퀀싱 시장은 유전체 기술의 발전, 시퀀싱 비용의 감소, 정밀의료, 진단, 맞춤형 의료에 대한 유전체 데이터의 적용 확대로 인해 빠르게 성장하고 있습니다. 전게놈 시퀀싱(WGS)은 생물의 전체 유전자 구성에 대한 종합적인 인사이트을 제공합니다. 반면, 전체 엑솜 시퀀싱(WES)은 유전자의 코드 영역에 초점을 맞추고 질병 메커니즘을 이해하는 데 매우 중요합니다. 종양학, 희귀질환 진단, 약물유전체학 분야의 유전자 검사에 대한 수요 증가, 유전체학 연구에 대한 투자 증가, 정부의 유전체 연구 지원 정책으로 인해 시장이 활성화되고 있습니다. 그 결과, 임상 현장에서 WGS와 WES의 통합이 더욱 보편화되고 있으며, 혁신적인 헬스케어 솔루션과 환자 결과 개선의 길을 열어가고 있습니다.
세계의 전게놈 및 엑솜 시퀀싱 시장에 대해 조사했으며, 시장의 개요와 제품별, 워크플로우별, 용도별, 최종사용자별, 지역별 동향 및 시장에 참여하는 기업의 개요 등을 제공하고 있습니다.
Introduction of Whole Genome and Exome Sequencing
Whole genome sequencing (WGS) and exome sequencing (WES) are cutting-edge genomic technologies that enable comprehensive analysis of an organism's genetic material. WGS involves sequencing the entire genome, encompassing both coding and non-coding regions, providing a complete genetic blueprint. In contrast, WES focuses on sequencing only the exonic regions, which are the protein-coding parts of the genome, representing about 1-2% of the genome but containing the majority of known disease-related variants. These technologies have revolutionized genomics by offering unprecedented insights into genetic variation, disease mechanisms, and evolutionary biology. Their applications span clinical diagnostics, personalized medicine, oncology, rare disease research, and more, driving significant advancements in healthcare and biomedical research. With continuous technological improvements, decreasing costs, and expanding applications, WGS and WES are becoming indispensable tools in modern genomics.
Market Introduction
| KEY MARKET STATISTICS | |
|---|---|
| Forecast Period | 2024 - 2033 |
| 2024 Evaluation | $2,101.2 Million |
| 2033 Forecast | $7,467.6 Million |
| CAGR | 15.13% |
The global whole genome and exome sequencing market, initially valued at $1,873.8 million in 2023, is poised for substantial growth, projected to reach $7,467.6 million by 2033, marking a remarkable compound annual growth rate (CAGR) of 15.13%. This surge reflects the escalating demand for personalized medicine and the increasing prevalence of genetic disorders worldwide. Hereditary genetic testing, a pivotal component of precision healthcare, enables individuals to assess their genetic predispositions to various diseases, empowering them and healthcare providers with invaluable insights for proactive intervention and tailored treatment strategies. As advancements in technology continue to enhance the accuracy and accessibility of genetic testing, the market is primed to revolutionize healthcare delivery, ushering in an era of preventive and personalized medicine on a global scale.
The whole genome and exome sequencing market has been experiencing rapid growth driven by advancements in genomic technologies, decreasing sequencing costs, and the expanding applications of genomic data in precision medicine, diagnostics, and personalized healthcare. Whole genome sequencing (WGS) provides comprehensive insights into the entire genetic makeup of an organism. In contrast, whole exome sequencing (WES) focuses on the coding regions of genes, which are crucial for understanding disease mechanisms. The market has been fueled by increasing demand for genetic testing in oncology, rare disease diagnosis, pharmacogenomics, rising investments in genomics research, and favorable government initiatives supporting genetic research. As a result, the integration of WGS and WES in clinical practice is becoming more prevalent, paving the way for innovative healthcare solutions and improved patient outcomes.
Industrial Impact
The industrial impact of the whole genome and exome sequencing market has been profound, significantly influencing various sectors, including healthcare, pharmaceuticals, biotechnology, and research. In healthcare, the adoption of these sequencing technologies has been transforming diagnostics and treatment strategies by enabling precise identification of genetic mutations and tailored therapeutic interventions. This precision medicine approach not only enhances patient care but also reduces healthcare costs by minimizing trial-and-error treatments. In the pharmaceutical industry, whole genome and exome sequencing have been pivotal in drug discovery and development, allowing for the identification of novel drug targets and biomarkers, thereby accelerating the development of targeted therapies. Biotechnology companies are leveraging these technologies to advance research in gene editing, synthetic biology, and agricultural biotechnology, leading to innovations in crop improvement and sustainable agriculture. Moreover, the increasing use of sequencing in academic and clinical research has been driving scientific discoveries and expanding one's understanding of genetic diseases and human biology. Overall, the integration of whole genome and exome sequencing across these industries is fostering innovation, improving efficiency, and opening new avenues for economic growth and development.
Market Segmentation
Segmentation 1: by Product
In the global whole genome and exome sequencing market, as of 2023, the kits segment holds the largest share at 62.83%. This dominance can be attributed to the essential role kits play in the sequencing process, encompassing DNA extraction, library preparation, and target enrichment, which are crucial for accurate and efficient sequencing. Kits are widely adopted due to their ease of use, reliability, and cost-effectiveness, streamlining laboratory workflows and ensuring consistent results. This rapid growth is expected to be driven by the increasing need for advanced bioinformatics tools and data analysis services to handle the vast amounts of data generated by sequencing technologies. Software solutions enhance data management, interpretation, and visualization, while services provide technical support, training, and consultancy, making sequencing data more accessible and actionable for clinical and research applications.
Segmentation 2: by Workflow
Based on workflow, the global whole genome and exome market was led by the WES segment, which held a 64.92% share in 2023. The whole exome sequencing (WES) workflow begins with the extraction, isolation, and purification of DNA from biological samples such as blood or saliva. This is followed by library preparation, where the DNA is fragmented and adaptors are added, and library quantification to ensure accurate DNA concentration. Next, target enrichment involves hybridizing the DNA library with probes that capture the exonic regions, enriching these target sequences. The enriched library is then sequenced using next-generation sequencing (NGS) technology. The resulting data undergoes bioinformatics analysis, where it is aligned to a reference genome, and genetic variations are identified, annotated, and interpreted for their potential impact on gene function and disease association.
Segmentation 3: by Application
Segmentation 4: by End User
In the global whole genome and exome sequencing (WGS and WES) market, as of 2023, the research and academic institutes segment holds the largest share at 39.69%, driven by extensive use in genomic research, significant government funding, and collaborative projects that advance scientific understanding of genetic diseases.
Segmentation 5: by Region
The whole genome and exome market in the North America region is expected to witness a significant growth rate of 14.80% during the forecast period, marked by the increasing prevalence of genetic disorders and the growing demand for personalized medicine and robust government initiatives. However, the Asia-Pacific region is expected to reach $1,784.8 million in 2033 from $372.9 million in 2023, at a CAGR of 17.26% during the forecast period 2024-2033.
Recent Developments in the Whole Genome and Exome Market
Demand - Drivers, Challenges, and Opportunities
Market Demand Drivers:
Growing Applications of Whole Genome and Exome Sequencing in Clinical Diagnostics: The increasing clinical applications of whole genome sequencing (WGS) and whole exome sequencing (WES) are significantly influencing the overall sequencing market. The adoption of WGS in clinical diagnostics for rare diseases is providing a more comprehensive genetic analysis compared to traditional methods. According to a study, "Whole Exome and Genome Sequencing in Mendelian Disorders: A Diagnostic and Health Economic Analysis," published in Nature Journal in August 2022, WGS can detect a broader range of genetic variants, including those in non-coding regions, which are often missed by WES. This comprehensive detection capability improves diagnostic accuracy, thereby enhancing patient care and outcomes.
Market Challenges:
Privacy and Ethical Concerns due to Increased Risk of Security Breaches: Ethical concerns related to privacy, confidentiality, and the return of results are prominent in the context of sequencing and must be addressed during the informed consent process. The method of data storage is crucial in managing privacy risks for participants. Privacy and ethical concerns have become significant challenges in the whole genome and exome sequencing market, especially with the increasing risk of security breaches.
Market Opportunities:
Increasing Usage of Sequencing Methodologies in Emerging Markets: The increasing application of whole genome and whole exome sequencing in developing countries presents a significant growth opportunity for the global market. As these technologies become more affordable and accessible, they are being integrated into healthcare systems in regions that were previously limited by cost and infrastructure. The availability of these advanced sequencing methods allows for the precise diagnosis and treatment of genetic diseases, which can significantly improve healthcare outcomes in these regions. This integration is facilitated by international collaborations and support from global health initiatives, which aim to enhance the capabilities of local healthcare providers.
How can this report add value to an organization?
Product/Innovation Strategy: The report offers in-depth insights into the latest technological advancements and emerging applications in genome and exome sequencing, enabling organizations to drive innovation and develop cutting-edge products tailored to market needs.
Growth/Marketing Strategy: By providing comprehensive market analysis and identifying key growth opportunities, the report equips organizations with the knowledge to craft targeted marketing strategies and expand their market presence effectively.
Competitive Strategy: The report includes a thorough competitive landscape analysis, helping organizations understand their competitors' strengths and weaknesses and allowing them to strategize effectively to gain a competitive edge in the market.
Methodology
Key Considerations and Assumptions in Market Engineering and Validation
Primary Research:
The primary sources involve industry experts in whole genome and exome, including the market players offering products and services. Resources such as CEOs, vice presidents, marketing directors, and technology and innovation directors have been interviewed to obtain and verify both qualitative and quantitative aspects of this research study.
The key data points taken from the primary sources include:
Secondary Research
Open Sources
The key data points taken from the secondary sources include:
Key Market Players and Competition Synopsis
Profiled companies have been selected based on inputs gathered from primary experts and analyzing company coverage, product portfolio, and market penetration.
In 2023, Illumina, Inc. held major share of the whole genome and exome sequencing market, reflecting its leading position and extensive portfolio of advanced sequencing technologies. Thermo Fisher Scientific Inc., Qiagen N.V., Pacific Biosciences (PacBio) and Oxford Nanopore Technologies plc are the other major players with, leveraging its broad range of genomic solutions and strong market presence. The companies are recognized for their innovative sequencing technologies that provide unique capabilities in long-read sequencing and real-time analysis. The competitive landscape, with Illumina leading significantly while other key players continue to innovate and capture niche segments within the market.
Some prominent names established in this market are:
Scope and Definition