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세계의 차세대 시퀀싱(NGS) 서비스 시장 : 기술, 용도, 최종 사용자, 서비스 유형, 지역별(2024-2031년)Next-Generation Sequencing Services Market By Technology, Application, End-User (Hospitals and Clinics, Contract Research Organizations ), Service Type, & Region for 2024-2031 |
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차세대 시퀀싱(NGS) 서비스에 대한 수요 증가는 맞춤형 의료 및 진단에 대한 파괴적인 영향으로 인한 것입니다. 진단 및 치료에 접근하는 방법을 변경했습니다. NGS는 전체 유전체 또는 선택 선택 영역의 신속하고 신뢰성 있는 시퀀싱을 가능하게 함으로써, 표적 의약품에 정보를 제공할 수 있는 유전자 변화의 검출을 가능하게 하고, 그 결과 시장은 2024년에 95억 3,000만 달러의 수익 돌파하고 2031년에는 약 183 억 5,000만 달러의 평가에 도달하여 환자의 결과를 개선할 것으로 예상됩니다.
예방 헬스케어 중시 증가가 NGS 서비스 수요를 밀어 올리고 있습니다. 조기 개입을 가능하게합니다. 게놈약학 분야에서 특히 중요하며 NGS는 개인이 특정 의약품에 어떻게 반응하는지 예측하는데 사용되기 때문에 2024년부터 2031년에 걸쳐 21.25%의 연평균 복합 성장률(CAGR)로 시장이 성장한다는 것을 가능하게 할 것입니다.
차세대 시퀀싱(NGS) 서비스는 DNA 또는 RNA의 신속한 시퀀싱을 가능하게하고 유전자 정보를 대규모로 평가하는 첨단 유전체 기술입니다. 의료 등 폭넓은 용도로 필요한 유전자 변이, 돌연변이, 유전자 발현에 관한 중요한 통찰을 줍니다.
차세대 시퀀싱(NGS) 서비스에는 유전학, 의료 진단, 맞춤형 의료 등 수많은 용도가 있습니다. NGS는 유전체 전체 또는 특정 영역의 신속하고 높은 처리량 시퀀싱를 가능하게 하고, 암, 낭포성 섬유증, 심혈관 질환 등의 질병을 유발하는 유전자 변이에 대한 광범위한 정보를 밝혀줍니다.
차세대 시퀀싱(NGS) 서비스의 향후 사용은 맞춤형 의료 및 유전체학를 포함한 건강 관리의 많은 측면을 변화시킬 것으로 기대되고 있습니다. NGS는 상세한 종양 프로파일링을 제공하고 암 증식을 일으키는 특정 유전자 이상을 발견할 수 있습니다.
차세대 시퀀싱(NGS) 서비스의 이용은 주로 맞춤형 의료에서의 응용 증가, 유전체 연구의 진보, 시퀀싱 기술 비용의 저하에 의해 추진되고 있습니다. 다양한 용도로 NGS의 이용을 촉진하고 있습니다. 맞춤형 의료는 NGS 서비스 보급의 주요 추진력입니다. 이상이 맞춤형 의료로, 그 대부분은 NGS 기술을 이용해 개발된 것입니다.
미국 국립 인간 유전체 연구소(NHGRI)에 따르면, 인간 유전체의 염기 시퀀싱에 드는 비용은 2001년 약 1억 달러에서 2022년에는 1,000 달러 이하로 10만분의 1로 떨어졌습니다. 또 다른 중요한 요인은 암 연구와 치료에서 NGS의 응용이 확대되고 있다는 것입니다. 미국 국립암 연구소의 암 유전체 아틀라스(TCGA)는 33개 암종에서 채취한 2만 개 이상의 원발성 암과 그에 적합한 정상 샘플을 평가하기 위해 NGS 기술을 사용했습니다. 종양학에서 이러한 광범위한 용도는 NGS 서비스 산업을 전진하고 있습니다.
윤리적 및 법적 고려사항은 차세대 시퀀싱(NGS) 서비스 분야의 확대에 큰 영향을 미칩니다. 주요 윤리적 고려사항 중 하나는 프라이버시와 유전자 데이터의 취급입니다. NGS 서비스에는 인간 유전체 시퀀싱이 포함되어 있으므로 적절하게 보호되지 않으면 악용될 수 있는 민감한 개인 정보가 생성됩니다. 유전자 데이터에 대한 무단 접근은 고용과 보험에서 유전적 차별과 같은 악용과 관련된 문제를 일으킵니다.
법적 문제는 NGS 서비스 사업에 특히 규제 준수 및 지적 재산권 측면에서 장애물입니다. NGS 기술의 진보에 따라 유전체 정보의 이용을 관리하는 법적 틀은 계속 진화하고 있습니다. 국가는 정책에 일관성이 없기 때문에 국제 공동 연구를 방해하고 시장 성장을 제한합니다. 기업은 복잡한 특허 규제, 특히 유전체 서열과 NGS 관련 기술의 소유권에 관한 규제를 관리해야 합니다. 또한, 인간 유전자와 특정 유전체 서열의 특허를 둘러싼 법정 투쟁은 기술 혁신을 방해하고 중요한 NGS 서비스에 대한 접근을 제한할 수 있습니다.
The growing demand for next-generation sequencing (NGS) services is largely due to its disruptive impact on personalized medicine and diagnostics. NGS has transformed how healthcare providers approach disease diagnosis and therapy, especially in oncology, genetic disorders, and infectious diseases. NGS enables the speedy and reliable sequencing of complete genomes or select areas allowing the detection of genetic alterations that can inform targeted medicines, hence improving patient outcomes by enabling the market to surpass a revenue of USD 9.53 Billion valued in 2024 and reach a valuation of aroundUSD 18.35 Billion by 2031.
The increased emphasis on preventative healthcare is driving up the demand for NGS services. As healthcare systems turn toward disease detection and prevention, NGS provides comprehensive genomic screening, identifying predispositions to specific ailments and allowing for earlier interventions. This is especially crucial in the field of pharmacogenomics where NGS is used to anticipate how individuals will react to specific pharmaceuticals, hence reducing bad drug responses by enabling the market to grow at aCAGR of 21.25% from 2024 to 2031.
Next Generation Sequencing (NGS) services are advanced genomic technologies that enable quick sequencing of DNA or RNA to evaluate genetic information on a massive scale. NGS services give critical insights into genetic variants, mutations, and gene expression which are required for a wide range of applications including medical research and diagnostics, drug discovery, and personalized medicine.
Next Generation Sequencing (NGS) services have numerous uses including genetics, medical diagnostics, and customized medicine. One of the most common applications is genetic testing, which identifies inherited genetic abnormalities, mutations, and disease propensity. NGS enables quick, high-throughput sequencing of entire genomes or particular areas revealing extensive information about genetic variants that contribute to disorders including cancer, cystic fibrosis, and cardiovascular disease.
The future usage of next-generation sequencing (NGS) services is expected to transform numerous aspects of healthcare including personalized medicine and genomics. One of the most promising applications is cancer diagnosis and treatment where NGS may give detailed tumor profiling and pinpoint particular genetic abnormalities that cause cancer growth.
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The use of next-generation sequencing (NGS) services is being pushed primarily by increased applications in personalized medicine, advances in genomic research, and lower sequencing technology costs. These characteristics are driving the usage of NGS in a variety of healthcare and life sciences applications. Personalized medicine is a primary driver of NGS service uptake. According to the U.S. Food and Drug Administration (FDA), as of 2022, more than 25% of new pharmaceuticals approved in the past five years were personalized medicines many of which were developed using NGS technologies.
According to the National Human Genome Research Institute (NHGRI), the cost of sequencing a human genome has dropped from approximately USD 100 Million in 2001 to less than $1,000 in 2022, a 100,000-fold decrease. Another key factor is the growing application of NGS in cancer research and treatment. The National Cancer Institute's Cancer Genome Atlas (TCGA) used NGS technology to evaluate over 20,000 primary cancers and matched normal samples from 33 cancer types. This widespread application in oncology is driving the NGS services industry forward.
Ethical and legal considerations have a substantial impact on the expansion of the next generation sequencing (NGS) services sector. One of the main ethical considerations is privacy and the handling of genetic data. Because NGS services include the sequencing of human genomes, sensitive personal information is generated which could be misused if not appropriately protected. Unauthorized access to genetic data raises issues about misuse such as genetic discrimination in employment or insurance.
Legal problems also pose hurdles for the NGS services business, particularly in terms of regulatory compliance and intellectual property rights. As NGS technology progresses, the legal framework governing genomic information use continues to evolve. Inconsistent policies across countries hamper international collaborations and limit market growth. Companies must manage complex patent regulations, particularly those governing ownership of genomic sequences and NGS-related technologies. Furthermore, legal battles over the patenting of human genes or specific genomic sequences can stifle innovation and restrict access to critical NGS services.
Whole genome sequencing (WGS) is a dominating technology in the next-generation sequencing (NGS) services industry due to its comprehensive nature and wide range of applications across industries. The ability to study genetic variations, mutations, structural changes, and functional elements across the entire genome providing insights into complex biological processes, disease mechanisms, and personalized medicine applications is increasing the use of WGS by researchers, clinicians, and organizations.
In addition, its involvement in discovering novel genetic markers, biomarkers, disease-causing mutations, and therapeutic targets for expanding our understanding of genetic features, hereditary diseases, complex disorders, and genetic predispositions will further accelerate the usage of WGS. In clinical diagnostics and healthcare, WGS is critical for genetic testing, illness diagnosis, and tailored medication. This allows clinicians to identify disease-causing mutations, analyze genetic risk factors, diagnose uncommon genetic illnesses, predict therapy responses, and adapt medicines to individual genomic profiles.
In What Ways are Hospitals and Clinics Driving the Growth of the Next-Generation Sequencing (NGS) Services Market?
The increase in demand for NGS services in hospitals and clinics for a wide range of clinical diagnostic applications including prenatal screening, pharmacogenomics, cancer genomics, rare illness detection, and infectious disease testing is a market profitable factor. NGS enables clinicians to perform the necessity for doctors to conduct complete genomic profiling of patient samples and find genetic mutations, structural variants, and biomarkers to provide accurate prognosis, treatment response, and disease risk data is expected to drive market expansion.
By incorporating genomic information into clinical decision-making, hospitals and clinics can improve treatment outcomes, reduce adverse medication responses, and increase patient happiness and quality of life. Genomic medicine research is widely conducted at hospitals and university medical institutes to improve scientific understanding of hereditary illnesses, molecular pathways, and therapeutic targets. NGS services contribute significantly to genomic research projects by facilitating large-scale DNA sequencing, genome-wide association studies (GWAS), and functional genomics experiments.
North America dominates the next generation sequencing (NGS) services market owing to its advanced healthcare infrastructure and major investments in precision medicine. The Precision Medicine Initiative, initiated by the US government in 2015 with an initial USD 215 Million commitment, has been a significant driver of NGS uptake. The National Institutes of Health's (NIH) "All of Us" Research Program, which is part of this project, seeks to collect genetic data from one million Americans and has already registered over 500,000 people as of 2023.
The NIH's Undiagnosed Diseases Network has employed NGS to diagnose 35% of cases, demonstrating the technology's utility. Furthermore, the Centers for Medicare & Medicaid Services (CMS) enhanced coverage for NGS-based diagnostic tests for individuals with hereditary ovarian or breast cancer in 2020, possibly benefiting up to 100,000 Medicare patients per year. This coverage expansion is projected to dramatically increase the use of NGS services in clinical settings. According to the Centers for Disease Control and Prevention (CDC), more than 1.8 million SARS-CoV-2 genomes will have been sequenced in the United States by 2022, demonstrating the importance of NGS in disease surveillance and pandemic response.
The Asia Pacific region is seeing the highest growth in the next generation sequencing (NGS) services market owing to increased demand for genomic therapies and whole-genome sequencing. Significant government funding, increased research activity, and the region's expanding prevalence of genetic illnesses all contribute to its rapid growth. This investment has already paid off with the number of whole-genome sequencing studies in China increasing by 120% between 2015 and 2020, according to the National Center for Biotechnology Information (NCBI).
Another important factor is the region's rising prevalence of genetic diseases. According to the World Health Organization (WHO), the incidence of genetic disorders in Asia is 53.5 per 1,000 live births which is higher than the global average of 39.7. This has resulted in an increased demand for genetic testing and tailored medicine. Since 2017, the South Korean government's Genome Technology to Business Translation Program has invested USD 70 Million in 100 genomics-based startups. Australia's Genomes Health Futures Mission which is part of the Medical Research Future Fund has committed AU$500 million over ten years to genomes research, with AU$150 million already funded by 2023.
The Next Generation Sequencing (NGS) Services Market is a dynamic and competitive space, characterized by a diverse range of players vying for market share. These players are on the run for solidifying their presence through the adoption of strategic plans such as collaborations, mergers, acquisitions, and political support. The organizations are focusing on innovating their product line to serve the vast population in diverse regions.
Some of the prominent players operating in the next-generation sequencing (NGS) services market include:
Quest Diagnostics Incorporated
ARUP Laboratories
Applied Biological Materials, Inc.
Novogene Co, Ltd.
Azenta Life Sciences (GENEWIZ)
NanoString
Illumina, Inc.
PacBio
Veritas
BGI (Beijing Genomics Institute)
Gene by Gene Ltd.
Lucigen Corporation
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