The global Next Generation Sequencing market was valued at USD 8.26 Billion in 2022 and growing at a CAGR of 19.24% from 2023 to 2032. The market is expected to reach USD 48.01 Billion by 2032. The next-generation sequencing technologies (NGS) market has grown significantly since it was first commercialized. This technology is massively parallel, providing ultra-high scalability, throughput and speed. It is used for finding the ordering of nucleotides in the targeted areas of DNA or RNA or complete genomes. NGS has completely transformed the biological sciences, helping the labs to work on a wide variety of applications and research on biological systems at a level that was not possible earlier. NGS helps the lab rapidly sequence the whole genomes and deeply sequence the target regions. It also has the application of using RNA sequencing for discovering novel RNA variants and merging the sites. It is also used for quantifying mRNAs for gene expression analysis. In the lab, it also helps in analyzing epigenetic factors like DNA protein interactions and genome-wide DNA methylation. It is used in the labs for sequencing cancer samples and studying rare somatic variants and tumour subclones. It is also used to study the human microbiome and identify novel pathogens.
Next-generation sequencing (NGS) is a parallel processing method that determines the sequence of nucleotides in the full genome with fast speed, scalability, and ultra-high capacity. Also, the NGS is slowly being used in medical laboratory research, disease diagnosis and screening in the healthcare sector. It is broadly used for personalized medicine, and it helps accelerate the drug research process. The unmet clinical requirement for a better tool for predicting, treating, diagnosing, and monitoring disease and progressively efficient sequencing technologies are some of the factors driving the Next Generation Sequencing Market. Also, a growing understanding of the molecular basis of disease, investment by the industries, patient demand and the regulations that support the marketing of tests without the need for FDA authorization fuel the market's growth. Different potential sequencing techniques like RNA sequencing, whole exome and targeted sequencing and whole-genome sequencing, among others, are broadly used by researchers to obtain a complete sample analysis. Also, compared to conventional Sanger sequencing technology, the NGS is less costly and offers increased throughput for DNA sequencing. The surge in the automation for the pre-sequencing protocols, post-sequencing protocols, and data study is positively influencing the NGS market. Using novel platforms for developing personalized medicine by medical analysis at the genetic level also enhances the demand for the NGS market. Hence, the growing focus on personalized medicine and companion diagnostics, advancements in technology like cloud computing and data integration, and the growing availability of genomic and proteomic data offer huge opportunities for the Next Generation Sequencing market. NGS diagnostic methods can potentially find the virus's genomic sequence and thus help scientists understand the mutations. Also, during the COVID-19 pandemic, governments worldwide collaborated with the corporate sector for the introduction of NGS technology as a properly functioning diagnostic tool in the market.
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This study forecasts revenue at global, regional, and country levels from 2019 to 2032. The Brainy Insights has segmented the global Next Generation Sequencing market based on below mentioned segments:
Global Next Generation Sequencing Market by Technology:
Global Next Generation Sequencing Market by Application:
Global Next Generation Sequencing Market by End User:
Global Next Generation Sequencing by Region:
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