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Carrier Screening Market is Estimated to Witness High Growth Owing to Opportunity of Increasing Incidence of Genetic Disorders

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Saya Bonde
Carrier Screening Market is Estimated to Witness High Growth Owing to Opportunity of Increasing Incidence of Genetic Disorders

Carrier screening refers to a genetic test that identify whether a person carries a genetic variant associated with a certain genetic disorder. A carrier is a person who harbors a genetic variant but does not display any symptoms of the associated genetic disease. Carrier screening is usually performed before or during pregnancy to determine the risk of having a baby with a genetic disorder. The global carrier screening market includes tests such as carrier screening for Cystic fibrosis, spinal muscular atrophy, fragile X syndrome. These tests aid in screening and detection of gene mutations to identify prospective parents who are carriers of genetic disorders. The global carrier screening Market is estimated to be valued at US$ 2.34 Bn in 2023 and is expected to exhibit a CAGR of 17% over the forecast period 2023 to 2030.

Market Opportunity:

The increasing incidence of genetic disorders globally presents a lucrative opportunity for growth of carrier screening market. Though a relatively small percentage of the general population carry such disorders, carrier screening can identify them and help reduce risk of having children with genetic disorders. According to data, approximately 1 in 30 individuals are carriers of diseases such as Cystic fibrosis, Tay-Sachs disease and Canavan disease. With increasing awareness among prospective parents regarding the benefits of carrier screening, more individuals are opting for these tests. This is estimated to increase the demand for carrier screening over the forecast period and drive the market growth.

Porter's Analysis

Threat of new entrants: New companies face high costs for screening, testing and genetic analysis equipment and technological capabilities. Regulatory barriers add to costs.

Bargaining power of buyers: Individual consumers have little bargaining power as a screening is typically covered by insurance.

Bargaining power of suppliers: Suppliers of screening kits and testing services have some power as the market is consolidating around large players.

Threat of new substitutes: No close substitutes exist currently as carrier screening offers unique health benefits over prenatal or postnatal testing.

Competitive rivalry: The market is growing rapidly attracting new players but competition is intensifying among major players.

SWOT Analysis

Strengths: Non-invasive screening technology. Growing awareness and demand. Risk assessment accuracy improving.

Weaknesses: High costs. Coverage limitations. Complexity of genomics understanding.

Opportunities: Expanding to new population segments and geographical regions. Integration with obstetric practices.

Threats: Regulatory hurdles. Technological disruptions. Ethical concerns around expanding scope.

Key Takeaways

The global carrier screening market size is expected to reach US$ 8.29 Bn by 2030, rising at a CAGR of 17% during the forecast period.

Regional Analysis: North America dominates currently due to advances in genomics and favorable policies. However, Asia Pacific is emerging as the fastest growing region on back of rising healthcare spend, growing middle class and increasing awareness.

Key players operating in the carrier screening market are Eurofins Scientific (US), Invitae (US), OPKO Health (US), Fulgent Genetics (US), Quest Diagnostics (US), Sema4 (US), Myriad Genetics (US), Illumina (US), and Thermo Fisher Scientific (US). These players are focusing on product development and strategic acquisitions to gain market share. For instance, Invitae acquired genetic testing companies like YouScript and Diploid to expand its carrier screening portfolio.

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