Carrier Screening Market, by Test Type (Expanded Carrier Screening and Targeted Disease Carrier Screening), by Disease Type (Cystic Fibrosis, Sickle Cell Disease, Spinal Muscular Atrophy, Fragile X Syndrome, Thalassemia, and Others), by End User (Hospitals, Reference Laboratories, and Others), and by Region (North America, Latin America, Europe, Asia Pacific, Middle East, and Africa) - Size, Share, Outlook, and Opportunity Analysis, 2019 – 2027

Genetic disorders are diseases caused due to change in the normal DNA sequence. These changes are known as mutations, which can occur in one or multiple genes. A person carries genes in pair, one from each parent. The person carrying the mutated gene for the genetic disorder is known as the carrier. If both the parents are carriers of the gene associated with the genetic disorder, then there is 25% chance that the child will be born with the disorder. If only one parent is the carrier of the mutated gene then there is 50% chance that the child will be carrying the mutated gene.

Carrier screening is a type of test which helps in determining the risk of having a child with a genetic disease. Carrier screening determines whether a healthy person carries the recessive gene of genetic diseases such as cystic fibrosis, sickle cell disease, and others.

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Global Carrier Screening Market – Dynamics

Rising mergers, agreements, and acquisitions by market players are expected to drive the global carrier screening market over the forecast period. For instance, in July 2017, Counsyl, Inc., entered into an expanded agreement with Angsana Molecular & Diagnostics Laboratory, a multinational laboratory services company, to commercialize expanded carrier screening (ECS) test in Hong Kong. Furthermore, in July 2018, Counsyl, Inc. was acquired by Myriad Genetics, Inc. The acquisition is expected to strengthen the genetic tests portfolio of Myriad Genetics, Inc.

Moreover, various launches and approvals of new carrier screening tests are likely to propel growth of the carrier screening market during the forecast period. For instance, in June 2018, Invitae Corporation, announced the launch of Invitae Carrier Screen, which is a test designed for enhanced risk assessment to determine the possibility of the child having a genetic disorder.

Global Carrier Screening Market – Regional Insights

North America accounted for the largest market share in 2018, owing to product approvals and launches of new carrier screening tests in the region. For instance, in October 2019, Sema4, announced the launch of Expanded Carrier Screen, a test which determines the risk of an inherited genetic disorder in the child.

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Europe is also witnessing lucrative growth in the carrier screening market owing to launches and approvals of new screening tests in the region. For instance, in June 2019, QIAGEN, a German provider of sample and assay technologies for molecular diagnostics, launched QIAseq Expanded Carrier Screening Panel. The QIAseq provides information about the targets and genes that are responsible for 200 disease indications.

Global Carrier Screening Market – Competitive landscape

Key players operating in the global carrier screening market include Invitae Corporation, Thermo Fisher Scientific, Quest Diagnostics, Sema4, Myriad Genetics, Inc., Illumina, Inc., Fulgent Genetics, Gene by Gene, CENTOGENE N.V., QIAGEN, Eurofins Scientific, Luminex Corporation, Medgenome, and others.

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