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Results for tag: "Carrier Screening"

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Human Genetics and Genomics. Edition No. 4 - Product Thumbnail Image

Human Genetics and Genomics. Edition No. 4

  • Book
  • January 2013
  • 288 Pages
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The Carrier Screening market within the context of Genomics is a rapidly growing field that focuses on the detection of genetic mutations that can cause inherited diseases. Carrier Screening tests are used to identify individuals who are carriers of a genetic mutation, even if they do not show any symptoms of the disease. This type of testing is often used to identify potential risks for couples planning to have children, as well as for individuals who have a family history of a particular genetic disorder. Carrier Screening tests are typically performed using a variety of methods, including next-generation sequencing, microarray-based testing, and Sanger sequencing. These tests can be used to detect a wide range of genetic mutations, including those associated with cystic fibrosis, sickle cell anemia, and Tay-Sachs disease. Some companies in the Carrier Screening market include Illumina, Myriad Genetics, Invitae, Counsyl, and GeneDx. Show Less Read more