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Results for tag: "Carrier Screening"

Carrier Screening - Global Strategic Business Report - Product Thumbnail Image

Carrier Screening - Global Strategic Business Report

  • Report
  • April 2024
  • 173 Pages
  • Global
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Carrier Screening Global Market Report 2024 - Product Thumbnail Image

Carrier Screening Global Market Report 2024

  • Report
  • February 2024
  • 200 Pages
  • Global
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Direct-to-Consumer (DTC) Genetic Testing Global Market Report 2024 - Product Thumbnail Image

Direct-to-Consumer (DTC) Genetic Testing Global Market Report 2024

  • Report
  • February 2024
  • 175 Pages
  • Global
From
Prenatal and Newborn Genetic Testing Global Market Report 2024 - Product Thumbnail Image

Prenatal and Newborn Genetic Testing Global Market Report 2024

  • Report
  • February 2024
  • 175 Pages
  • Global
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Global Prenatal Genetic Testing - Forecast to 2026 - Product Thumbnail Image

Global Prenatal Genetic Testing - Forecast to 2026

  • Report
  • October 2022
  • 70 Pages
  • Global
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Global Carrier Screening Market 2022-2026 - Product Thumbnail Image

Global Carrier Screening Market 2022-2026

  • Report
  • March 2022
  • 120 Pages
  • Global
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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