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市场调查报告书
商品编码
1666233
北美基因分型市场预测至 2031 年 - 区域分析 - 按产品类型、技术、应用和最终用户North America Genotyping Market Forecast to 2031 - Regional Analysis - by Product Type, Technology, Application, and End user |
2023 年北美基因分型市值为 120.4457 亿美元,预计到 2031 年将达到 629.0063 亿美元;预计 2023 年至 2031 年的复合年增长率为 23.0%。
遗传疾病和罕见疾病诊断应用推动北美基因分型市场发展
根据世界卫生组织 (WHO) 的数据,2050 年可能会出现约 3,500 万例新发癌症病例,比 2022 年的 2,000 万例增加 77%。这种疾病影响了超过600万各个年龄层的美国人。根据该协会的估计,截至 2022 年,650 万 65 岁以上的美国人患有阿兹海默症,其中 73% 年龄在 75 岁以上。根据《健康监测杂誌》发表的一项研究,全球有多达 3 亿人患有罕见疾病。儘管单一疾病很罕见,但它们共同为全球医疗保健系统带来了重大挑战。
由于癌症、阿兹海默症和罕见疾病在临床上难以识别,基因分型成为族群诊断检测的支柱。可以将从基因分型获得的 DNA 序列与样本或参考序列进行比较以确定变异。基因分型也用于检测单核苷酸多态性(SNP),即群体内遗传互补的微小变异。人类基因组拥有近6.6亿个SNP,这是最常见的遗传变异。此外,透过比较健康和患病人群的多态性,全基因组关联研究 (GWAS) 可以揭示常见疾病与 SNP 之间的关联。 GWAS 可以透过寻找可能的原因来解开潜在疾病状态的分子机制。 SNP 甚至存在于单细胞生物中,例如细菌。 SNP 基因分型可以区分微生物分离株,甚至可以用于识别抗生素抗药性菌株。基于SNP的菌株检测对各个药物和临床分析都有重大的影响,在传染病流行病学中也得到了应用。
北美基因分型市场概览
北美基因分型市场分为美国、加拿大和墨西哥。越来越多地采用技术先进的产品和解决方案以及不断涌现的研究和开发活动是该地区基因分型市场受益的因素。此外,政府主导的计画(例如「我们所有人的研究计画」)、各个基因组学界发起的倡议以及人们对基因分型服务的日益认识是推动北美市场扩张的主要驱动力。
北美基因分型市场收入及预测(百万美元)
北美基因分型市场细分
北美基因分型市场分为产品类型、技术、应用、最终用户和国家。
根据产品类型,北美基因分型市场分为仪器、试剂和试剂盒、生物资讯学和基因分型服务。试剂和试剂盒部分在 2023 年占据了最大的市场份额。
根据技术,北美基因分型市场分为微阵列、毛细管电泳、定序、聚合酶炼式反应(PCR)、基质辅助雷射解吸/MALDI-TOF 和其他技术。聚合酶链反应 (PCR) 领域在 2023 年占据了最大的市场份额。
根据应用,北美基因分型市场细分为药物基因组学、诊断和个人化医疗、动物遗传学、农业生物技术和其他应用。 2023 年,诊断和个人化医疗领域占据最大的市场份额。
就最终用户而言,北美基因分型市场分为製药和生物製药公司、诊断和研究实验室、学术机构和其他最终用户。 2023 年,製药和生物製药公司部门占据了最大的市场份额。
依国家划分,北美基因分型市场分为美国、加拿大和墨西哥。 2023 年美国占据北美基因分型市场的主导份额。
Hoffmann-La Roche Ltd、QIAGEN NV、Merck KGaA、Thermo Fisher Scientific Inc、BioTek Instruments, Inc、TRIMGEN CORPORATION、Illumina Inc、Danaher Corp、Bio-Rad Laboratories Inc、GE HealthCare Technologies Inc、Standard BioTools Inc、Laboratory Corp of America、Sooratory Corp.是北美基因分型市场的一些领导公司。
The North America genotyping market was valued at US$ 12,044.57 million in 2023 and is expected to reach US$ 62,900.63 million by 2031; it is estimated to record a CAGR of 23.0% from 2023 to 2031.
Use in Diagnosis of Genetic and Rare Diseases Fuels North America Genotyping Market
According to the World Health Organization (WHO), ~35 million new cancer cases are likely to occur in 2050, a 77% increase from the corresponding 20 million cases in 2022. In 2022, the Alzheimer's Association stated that the number of people living with Alzheimer's in the US is rapidly increasing. The disease affects more than 6 million Americans from all age groups. As per the association's estimates, 6.5 million Americans aged more than 65 suffered from Alzheimer's as of 2022, and 73% of this population was aged 75 or older. As per a study published in the Journal of Health Monitoring, up to 300 million people worldwide suffer from rare diseases. Although individual diseases are rare, they collectively pose significant challenges to the global healthcare system.
Since cancer, Alzheimer's disease, and rare diseases are difficult to identify clinically, genotyping stands as the backbone of diagnostic testing in the population. DNA sequences obtained from genotyping can be compared to sample or reference sequences to determine variations. Genotyping is also employed to detect single-nucleotide polymorphisms (SNPs), which are minor variations in genetic complement within the population. The human genome has nearly 660 million SNPs, which makes them the most widespread genetic variation. Moreover, by comparing polymorphisms in healthy and diseased populations, genome-wide association studies (GWAS) can uncover links between common illnesses and SNPs. GWAS can untangle the molecular mechanisms in underlying disease states by finding probable causes. SNPs are even present in single-celled organisms, such as bacteria. SNP genotyping can discriminate between microorganism isolates and could even be accustomed to identifying antibiotic-resistant strains. SNP-based strain detection has a significant impact on each pharmaceutical and clinical analysis, and it has also been used in infectious disease epidemiology.
North America Genotyping Market Overview
The North America genotyping market is segmented into the US, Canada, and Mexico. Increasing adoption of technologically advanced products and solutions, and surging research and development activities are the factors benefiting the genotyping market in this region. Moreover, government-led programs such as the "All of Us Research Program," initiatives by various genomic communities, and the increasing awareness of genotyping services are the key drivers of the market expansion across North America.
North America Genotyping Market Revenue and Forecast to 2031 (US$ Million)
North America Genotyping Market Segmentation
The North America genotyping market is categorized into product type, technology, application, end user, and country.
Based on product type, the North America genotyping market is segmented into instruments, reagents and kits, bioinformatics, and genotyping services. The reagents and kits segment held the largest market share in 2023.
By technology, the North America genotyping market is categorized into microarrays, capillary electrophoresis, sequencing, polymerase chain reaction (PCR), matrix-assisted laser desorption / MALDI-TOF, and other technologies. The polymerase chain reaction (PCR) segment held the largest market share in 2023.
Based on application, the North America genotyping market is segmented into pharmacogenomics, diagnostics and personalized medicine, animal genetics, agricultural biotechnology, and other applications. The diagnostics and personalized medicine segment held the largest market share in 2023.
In terms of end user, the North America genotyping market is bifurcated into pharmaceutical and biopharmaceutical companies, diagnostic and research laboratories, academic institutes, and other end users. The pharmaceutical and biopharmaceutical companies segment held the largest market share in 2023.
By country, the North America genotyping market is segmented into the US, Canada, and Mexico. The US dominated the North America genotyping market share in 2023.
Hoffmann-La Roche Ltd, QIAGEN NV, Merck KGaA, Thermo Fisher Scientific Inc, BioTek Instruments, Inc, TRIMGEN CORPORATION, Illumina Inc, Danaher Corp, Bio-Rad Laboratories Inc, GE HealthCare Technologies Inc, Standard BioTools Inc, Laboratory Corp of America Holdings, Beckman Coulter Inc, BGI, Takara Bio Inc, and DiaSorin SpA. are some of the leading companies operating in the North America genotyping market.