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"The global next generation sequencing market is expected to reach USD 19.70 billion by 2025 registering a CAGR of 12.78%. Growing application of NGS methodologies due to rising number of strategic developments initiated by the market participants is one of the key drivers of the market. These novel strategies mark the presence of intense competition between the key firms. Companies are further increasing their installation base by providing sequencing services in different emerging countries. For instance, in April 2018, Illumina entered into a partnership with Loxo Oncology for the development of Illumina TruSight Tumor 170 NGS test as a companion diagnostic for Loxo Oncology's LOXO-292 and larotrectinib for tumor profiling."

Next Generation Sequencing Market

Next Generation Sequencing Market Size - NGS Industry Report, 2025

Next Generation Sequencing Market Size | Global NGS Industry Report, 2028

A fresh report has been published and added, recently, in the massive database of Reports and Insights, which is developed using verified research methodologies and proven analytical approaches. The report determines diverse eminent factors and trends encouraging the market growth of the global Molecular Diagnostics Market. The research study is entitled "Molecular Diagnostics Market: Opportunity Analysis and Future Assessment 2022-2030", which profoundly examines the global market evolution, along with the in-depth knowledge of the future market potential and the statistics implicated in the development of the respective market during the forecast period of 2022-2030. For the avail and interest of the readers, the report arrives at the conclusion with a special emphasis on the comprehensive profiling of the leading players in the global Molecular Diagnostics Market. The global Molecular Diagnostics market is estimated to reach at a value of US$ 9.8 Bn by the end of 2020 and expected to reach at a value of US$ xx Bn by 2028 with a significant CAGR of 8.7% Request a Sample Copy of this Report @: https://reportsandinsights.com/sample-request/1386 Molecular Diagnostics Introduction Molecular diagnostics, also commonly known as molecular pathology, can be comprehended as a medical procedure that comprises taking samples of DNA or RNA from an individual's body, which is a exclusive genetic code found in human cells, and examining the patterns for danger signs that can identify and diagnose the probable emergence of a specific ailment. The molecular diagnostic tests are usually performed to figure out whether or not patients have a gene mutation related with a specific ailment, either as an hereditary or a captured mutation. The test can also be performed to determine a common inherited hereditary cancer. Hereditary disorders can be determined at the newborn, prenatal, and adult stages of life. In addition, the molecular diagnostics test is also performed when

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