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市場調查報告書
商品編碼
2016159
單核苷酸多態性(SNP)基因型鑒定市場報告:按技術、應用和地區分類(2026-2034 年)Single Nucleotide Polymorphism Genotyping Market Report by Technology, Application, and Region 2026-2034 |
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全球單核苷酸多態性(SNP)基因型鑒定市場在2025年達到130億美元。 IMARC Group預測,到2034年,該市場將達到452億美元,2026年至2034年的複合年成長率(CAGR)為14.41%。市場成長的主要促進因素包括與基因分型相關的研發活動的擴大、對個人化醫療和新型藥物遞送系統的需求不斷成長,以及對動植物材料基因分析的需求不斷成長。
單核苷酸多態性(SNP)基因型鑒定是一種透過檢測去氧核糖核酸(DNA)序列中的特定位點來識別和分析個體間遺傳變異的技術。它涉及識別個體DNA中特定SNP位點存在的特定核苷酸。此方法依賴聚合酵素鏈鎖反應(PCR)和DNA定序等先進的分子生物學技術。具體而言,PCR擴增含有SNP的DNA片段,然後透過直接定序擴增的DNA或使用其他方法(例如微陣列或等位基因特異性PCR)來識別SNP位點的核苷酸。這有助於理解群體遺傳學、遷移模式和演化歷史。它在確定藥物反應性、預測疾病易感性以及開發針對特定基因型的治療方法方面也發揮著至關重要的作用。研究人員利用SNP基因型鑒定來闡明複雜疾病的遺傳基礎、識別遺傳風險因子並開發先進的診斷工具。
目前,SNP基因型鑒定需求的不斷成長正在推動市場成長,這主要得益於基因分型研發活動的日益活躍以及生物資訊學在診斷工具和各種疾病有效治療方法開發中的應用。此外,SNP基因型鑒定在闡明癌症、心血管疾病、阿茲海默症和氣喘等多種人類疾病的發病機制方面的應用不斷擴展,也為市場帶來了良好的前景。同時,全球對SNP基因型鑒定的需求也不斷成長,用於建立遺傳關係、解決親子鑑定糾紛以及支持刑事調查。這些需求與蓬勃發展的醫療產業共同推動了市場成長。此外,個人化醫療和新型藥物遞送系統研發管線的擴展也帶動了藥物基因體學需求的成長,進一步促進了市場成長。生命科學領域眾多SNP基因型鑒定技術的應用,包括農業生物技術、診斷研究、製藥、藥物藥物基因體學學以及動物和牲畜育種等,也為市場成長做出了貢獻。全球範圍內糖尿病、心血管疾病和癌症發病率的不斷上升也對市場產生了積極影響。此外,對動植物飼料原料進行基因分析的需求日益成長,也推動了市場成長。
The global single nucleotide polymorphism (SNP) genotyping market size reached USD 13.0 Billion in 2025. Looking forward, IMARC Group expects the market to reach USD 45.2 Billion by 2034, exhibiting a growth rate (CAGR) of 14.41% during 2026-2034. The growing genotype research and development activities, rising demand for personalized medicine and novel drug delivery systems, and increasing demand for genetic analysis in animal and plant feedstock represent some of the key factors driving the market.
Single nucleotide polymorphism (SNP) genotyping is a technique designed to identify and analyze genetic variations among individuals by examining specific locations within their deoxyribonucleic acid (DNA) sequence. It involves determining the specific nucleotide present at a particular SNP site in the DNA of an individual. It relies on advanced molecular biology techniques, such as polymerase chain reaction (PCR) and DNA sequencing, wherein PCR amplifies the DNA segment containing the SNP, and then the nucleotide at the SNP site is determined either by directly sequencing the amplified DNA or using other methods like microarrays or allele-specific PCR. It aids in understanding population genetics, migration patterns, and evolutionary history. It plays a crucial role in determining response to medications, predicting disease susceptibility, and tailoring treatments to specific genetic profiles. SNP genotyping is used by researchers to study the genetic basis of complex diseases, identify genetic risk factors, and develop enhanced diagnostic tools.
At present, the increasing demand for SNP genotyping on account of the rising genotype research and development activities and bioinformatics in the development of diagnostic tools or effective therapeutics for various diseases represents one of the crucial factors supporting the growth of the market. In addition, the growing utilization of SNP genotyping in the etiology of various human diseases, such as cancer, cardiovascular, Alzheimer's, and asthma, is offering a favorable market outlook. Besides this, there is a rise in the demand for SNP genotyping to establish genetic relationships, resolve paternity disputes, and assist in criminal investigations around the world. This, along with the thriving medical industry, is propelling the growth of the market. Moreover, the increasing demand for pharmacogenomics due to the rising pipeline for personalized medicine and novel drug delivery systems is strengthening the growth of the market. Apart from this, numerous technologies of SNP genotyping in the life science field, such as agricultural biotechnology, diagnostic research, pharmaceuticals, pharmacogenomics, and animal and livestock breeding, are contributing to the growth of the market. In line with this, the growing prevalence of diabetes, cardiovascular diseases, and cancer across the globe is positively influencing the market. Furthermore, the rising demand for genetic analysis in animal and plant feedstock is bolstering the growth of the market.
The report has also provided a comprehensive analysis of all the major regional markets, which include North America (the United States and Canada); Asia Pacific (China, Japan, India, South Korea, Australia, Indonesia, and others); Europe (Germany, France, the United Kingdom, Italy, Spain, Russia, and others); Latin America (Brazil, Mexico, and others); and the Middle East and Africa. According to the report, North America was the largest market for single nucleotide polymorphism (SNP) genotyping. Some of the factors driving the North America single nucleotide polymorphism (SNP) genotyping market included favorable government policies towards proper diagnosis, increasing screening and treatment of fatal diseases, availability of enhanced research and development (R&D) facilities, etc.
The report has also provided a comprehensive analysis of the competitive landscape in the global single nucleotide polymorphism (SNP) genotyping market. Detailed profiles of all major companies have been provided. Some of the companies covered include Agilent Technologies Inc., Eurofins Genomics (Eurofins Scientific SE), Illumina Inc., Integrated DNA Technologies, Inc.(Danaher Corporation), LGC Limited, PREMIER Biosoft, Promega Corporation, QIAGEN N.V, Roche Holding AG, Thermo Fisher Scientific Inc., etc. Kindly note that this only represents a partial list of companies, and the complete list has been provided in the report.