市场调查报告书
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2030 年合成基因组学市场预测:按产品、应用、最终用户和地区进行的全球分析Synthetic Genomics Market Forecasts to 2030 - Global Analysis By Product (Adapters, DNA Template, Klenow Fragment, Modifying Enzymes, Primers and Other Products), Application, End User and By Geography |
根据 Stratistics MRC 的数据,2023 年全球合成基因组市场规模将达到 303 亿美元,预计到 2030 年将达到 787 亿美元,预测期内复合年增长率为 14.6%。
合成生物学是一个快速发展的领域,涉及遗传物质的生产和操作,包含在合成基因组学市场中。这个领域涉及创建、建构和改进用于多种用途的合成 DNA 序列,包括创建基因改造生物、人造细胞和客製化遗传电路。合成基因组学对于医学领域的药物开发、基因治疗和个体化医疗至关重要。在农业领域,它有助于创造具有更好特性的基因改造作物。
根据世界经济论坛 2021 年 9 月发布的资料,由于针对病毒的 mRNA 疫苗的开发,合成生物学的进步在控制流行病方面具有巨大潜力。
随着合成基因组学的快速发展,需要额外的研发资金来促进创新和新技术。这些投资用于资助 DNA 合成、基因编辑和其他遗传物质操作的尖端方法的探索。此外,公共和私营部门都认识到合成基因组在医疗保健、农业和工业应用中的巨大潜力,因此增加了对研究计画的财政支持。
由于基因工程复杂且需要尖端技术,中小型企业和研究机构被认为很难进入市场。创建先进的基因编辑工具、DNA合成技术和其他重要技术需要大量资金,这阻碍了许多人从事这一领域的工作。然而,公司在合成基因组学领域探索和创新的能力可能会受到大量初始投资和持续研发成本的限制。
合成基因组学是合成生物学的一个方面,它正在促进各个领域对创新和适应性生物解决方案不断增长的需求。随着公司和教育机构意识到合成基因组学在创造和修改遗传物质方面具有巨大潜力,对客製化生物系统的需求正在增加。这种需求的应用范围很广,包括工业生物技术、医疗保健、农业等。此外,利用合成基因组学,可以对生物体进行工程改造以执行特定任务,例如为工业过程创造生物基材料、具有改进特性的基因工程作物以及药物治疗。
由于操纵遗传物质和产生合成生物体的可能性,引起了人们对将合成基因组学用于邪恶目的的担忧。为了减轻这些担忧,政府和监管机构必须制定严格的法律,禁止非法取得基因技术。可能会製造出具有恶意目的的基因改造生物,例如生物武器,因此需要采取有效的安全预防措施。然而,由于这些担忧,合成基因组市场的公司难以管理合规性要求,减缓了监管核准流程并加强了审查。
全球健康危机已经证明了尖端基因技术在疫苗开发、诊断和替代疗法方面的重要性。合成基因组学使 mRNA 疫苗的快速发展成为可能,并证明该技术可以快速适应新出现的感染疾病。疫情推迟了研究倡议、扭转了供应链并将资源用于紧急医疗保健需求,间接影响了市场成长轨迹。资金筹措限制和经济不确定性影响了该行业规模较小的参与者。
由于 DNA 模板对于准确有效地合成遗传物质至关重要,因此它在合成基因组学市场中占据最大份额。 DNA 合成技术的进步,包括自动化 DNA 合成平台和创新方法,现在使研究和生物技术研究人员能够以前所未有的速度和精度设计和製造客製化的 DNA 序列。此外,各种应用(包括基因治疗、药物药物研发和基因改造牲畜的培育)对合成生物解决方案的需求不断增长,也是推动 DNA 模板领域兴起的因素。
由于器官移植在解决器官短缺相关挑战方面具有变革性作用,预计该产业在预测期内将出现盈利成长。为了解决与器官排斥和器官稀缺相关的问题,合成基因体学已成为生产具有更高相容性的器官和组织的有效方法。此外,精确基因工程器官的能力提供了为特定患者量身定制移植物、抑制免疫反应并提高移植成功率的潜力。
在预测期内,亚太地区占据了最大的市场份额。这是由于该地区经济的快速工业化和技术进步,以及人们日益认识到合成基因组学在许多领域的革命性潜力。中国、日本、印度等国家正在进行大规模的研发投入,为合成基因体学的发展创造了完美的环境。学术机构、研究机构和生物技术公司积极推动前沿倡议,以促进创新和新应用的创造。
随着对精准医疗和个人化医疗保健的日益关注,由于医疗保健相关计划的增加,亚太地区正在经历盈利成长。合成基因组学对于这些努力至关重要,因为它能够客製化遗传干预、基因疗法和诊断工具。合成基因组学技术的使用因其解决当地健康问题和提供定製药物疗法的潜力而受到推动。此外,新加坡和中国等国家的政府正在积极支持合成生物学和生物技术领域的努力,投入资源和基础设施来支持这些领域的研究和开发的进步。
According to Stratistics MRC, the Global Synthetic Genomics Market is accounted for $30.3 billion in 2023 and is expected to reach $78.7 billion by 2030 growing at a CAGR of 14.6% during the forecast period. The rapidly growing field of synthetic biology, which involves the production and manipulation of genetic material, is included in the Synthetic Genomics Market. It involves the creation, building, and refinement of synthetic DNA sequences for a variety of applications, including the creation of genetically modified creatures, artificial cells, and tailored genetic circuits. Synthetic genomics is essential to drug development, gene therapy, and customized medicine in the field of medicine. It aids in the creation of genetically engineered crops with enhanced attributes in agriculture.
According to a data published by the World Economic Forum in September 2021, the advancements in the synthetic biology have a vast potential to manage the pandemic for the development of mRNA vaccine against virus.
As synthetic genomics develops rapidly, additional funding for research and development is needed to promote innovation and new technologies. These investments fund the examination of cutting-edge methods for DNA synthesis, gene editing, and other genetic material manipulation. Additionally, growing financial support for research initiatives is a result of both the public and private sectors recognizing the enormous potential of synthetic genomes in healthcare, agriculture, and industrial applications.
Due to the complexity of genetic engineering and the requirement for cutting-edge technologies, smaller businesses and research institutions consider it difficult to enter the market. Significant money is needed to create advanced gene editing tools, DNA synthesis techniques, and other critical technologies, which prevents numerous individuals from working in this field. However, companies' capacity to explore and innovate in synthetic genomics may be constrained by the significant initial investment and ongoing research and development costs.
Synthetic genomics, a fundamental aspect of synthetic biology, contributes to the growing demand for innovative and adaptable biological solutions in a range of sectors. Customized biological systems are becoming more and more in demand as companies and educational institutions realize the enormous promise synthetic genomics has for creating and modifying genetic material. Applications for this demand are wide-ranging and include industrial biotechnology, healthcare, and agriculture. Moreover, with the use of synthetic genomics, biological organisms can be designed to do specific duties, such as creating bio-based materials for industrial processes, genetically modified crops with improved features, and medicinal treatments.
Fears regarding the exploitation of synthetic genomics for malevolent terminates are triggered by the manipulation of genetic material and the potential production of synthetic creatures. To mitigate these worries, governments and regulatory agencies must impose stringent laws that prohibit illegal access to genetic technologies. Effective safety precautions are necessary due to the possibility of creating genetically modified organisms with malicious intent, such as bioweapons. However, companies in the synthetic genome market find it difficult to manage compliance requirements as a result of these worries, which also slow down the regulatory approval process and raise scrutiny.
The relevance of cutting-edge genetic technologies for vaccine development, diagnostics, and treatment alternatives has been demonstrated by the global health crisis. The rapid development of mRNA vaccinations was made possible by synthetic genomics, demonstrating the technology's capacity to adapt rapidly to new infections. The pandemic managed to indirectly affect the market's growth trajectory by delaying research initiatives, reversing supply chains, and directing resources to urgent healthcare requirements. Funding limitations and economic uncertainty had an impact on the industry's smaller participants.
Due to its crucial significance in the accurate and effective synthesis of genetic material, the DNA template segment held the largest share in the synthetic genomics market. Researchers and biotechnologists can design and manufacture customized DNA sequences with previously unattainable speed and accuracy because of advancements in DNA synthesis technology, including automated DNA synthesis platforms and innovative approaches. Furthermore, the growing need for synthetic biology solutions for a variety of applications, such as gene therapy, drug discovery, and the generation of genetically modified livestock, is the factor that is causing this rise in the DNA template sector.
Because organ transplantation has a transformative effect on addressing the challenges associated with organ shortages, the segment is expected to grow profitably during the projected period. To address the issues associated with organ rejection and scarcity, synthetic genomics has emerged as a potentially efficient way of producing organs and tissues with improved compatibility. Additionally, the capacity to precisely modify organs genetically offers the possibility of customizing grafts for particular patients, reducing immunological reactions, and raising transplant success rates.
Over the course of the projected period, the Asia Pacific region had the largest share of the market due to the region's economies experiencing rapid industrialization and technological improvement, as well as the increasing awareness of the revolutionary potential of synthetic genomics across numerous sectors. Significant R&D investments have been made by nations like China, Japan, and India, creating an optimal environment for the development of synthetic genomics. Cutting-edge initiatives are being actively promoted by academic institutions, research organizations, and biotech corporations, which promote innovation and the creation of new applications.
With an increasing focus on precision medicine and tailored healthcare, the Asia-Pacific area is experiencing profitable growth as a result of an increase in healthcare-related projects. Because it renders it feasible to customize genetic interventions, gene therapies, and diagnostic tools, synthetic genomics is essential to these initiatives. The use of synthetic genomics technology is being propelled by its potential to address regional health concerns and offer customized medicinal therapies. Moreover, governments in nations like Singapore and China are actively supporting efforts in the domains of synthetic biology and biotechnology, offering resources and infrastructure to support the advancement of these fields' research and development.
Some of the key players in Synthetic Genomics market include Biocompare Inc , Boster Biological Technology, Eurofins Genomics, Genewiz, GenScript, Integrated DNA Technologies Inc, Synthetic Genomics Inc, Thermo Fisher Scientific Inc and Twist Bioscience .
In October 2023, Global genomics solutions provider Integrated DNA Technologies (IDT), an operating company in the Life Sciences segment of Danaher Corporation announced the completion of its new Therapeutic Oligonucleotide Manufacturing facility in Coralville, Iowa. The milestone marks a significant achievement in the company's 35-year-history-its entrance into the therapeutics space-and enables IDT to manufacture products for research use through to current good manufacturing practice (cGMP) grade cell and gene therapy reagents to provide researchers with a single partner that can help them rapidly transition from the lab to therapeutic development.
In February 2023, Ultima Genomics, Inc., a developer of a revolutionary new ultra-high throughput sequencing architecture, announced a strategic collaboration with global genomics solutions provider Integrated DNA Technologies (IDT) to enable key next generation sequencing (NGS) applications on Ultima platforms.
In February 2023, Twist Bioscience announces technology early access of enhanced whole genome sequencing solution at AGBT. eWGS is a novel solution that enables researchers to obtain simultaneous low-pass whole genome data together with deep coverage of selected regions, in a high-throughput and cost-effective workflow.