Genotyping Assay Market Demand Share Size Analysis 2022-2029

The Genotyping Assay Market is expected to grow at a CAGR of 19.99% during the forecast period 2022-2029. North America region has the highest market share in the Genotyping Assay Market, and it is further continuing its dominance during the forecast period.

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Our research report gives wide perceptions of the latest trends and development prospects of the market analysis, detailed segmentation analysis, volume, size, share, growth drives, and opportunities in the market. In-depth regional and country-level illustration of the competitive landscape depends on several phases and status of clinical trials over the prominent economies of the globe, and also report contains a number of major companies profiled in the relevant market.

Market Drivers:

Genotyping can be used to investigate large DNA structural changes and genetic variants like single nucleotide polymorphisms (SNPs). Microarrays and other high-throughput genomic technologies like next-generation sequencing (NGS) make it possible to gain a deeper comprehension of the molecular aetiology of disease.

An analysis needs to be both flexible and precise because there are multiple genomic targets that could cause a disease. SNP genotyping and copy number variation (CNV) data analysis tools can look at the results of millions of markers and probes and find sample outliers, revealing the functional effects of genetic variation. Understanding disease mechanisms, predicting an individual's risk of developing certain diseases, and even assisting in the development of personalized therapies can all be facilitated by genotyping. TaqMan SNP genotyping assays from Biosystems for Applied Research have been used to find variants that are linked to blood disorders and other diseases. The Taq polymerase enzyme, a double-stranded DNA template, and two forward and reverse primers specific to the amplified sequence are required for TaqMan SNP genotyping assays. SNP detection, in contrast to gene expression qPCR, requires the use of two probes with distinct fluorescent reporters. Samples with homozygous and heterozygous genotypes can be distinguished by this.

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Market Segmentation:

By Product:
• Reagents & Kits
• Instruments
• Other

By Technology:
• PCR, Microarrays
• Sequencing
• Capillary Electrophoresis
• Other

By End-User:
• Pharmaceutical and Biopharmaceutical Companies
• Diagnostic and Research Laboratories
• Other

Geographical Classification:
• North America
• Latin America
• Europe
• Asia Pacific
• Middle East
• Africa

Major Companies Listed:
Thermo Fisher Scientific, Illumina, QIAGEN, Agilent Technologies, LGC, Biosearch Technologies, Roche Diagnostics, Fluidigm Corporation, PerkinElmer, Bio-Rad Laboratories, Integrated DNA Technologies.

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This release was published on openPR.