Reproductive Genetics Market Size to Reach Valuation of USD 11.23 Billion in 2028 Growing at a CAGR of 12.3%, According to Latest Analysis by Emergen Research

The global reproductive genetics market size is expected to reach USD 11.23 Billion at a steady CAGR of 12.3% in 2028,.

The global reproductive genetics market size is expected to reach USD 11.23 Billion at a steady CAGR of 12.3% in 2028,. The market is expected to witness increased investment and growth owing to surge in demand for genetic testing and improvement in reimbursement for medical tests.

Reproductive genetics deal with relationship between reproduction and genotype. It studies the transmission of genetic material from one generation to the next and the effects of abnormalities in the genetic material. Increase in availability of next-generation technologies that allow early-stage screening of fetus during pregnancy for genetic disorders is another factor propelling growth of the market.

Reproductive genetics contributes to predicting and preventing genetic disorders during reproductive procedures. It offers vital information about the probability of having children with genetic specific disorders. Genetic makeup can lead to serious problems in reproduction, which creates the need for genetic diagnosis and counseling.

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Increasing preference for genetic testing of embryos during pregnancy and of those created through IVF to check for possible genetic disorders is driving growth of reproductive genetics market. The U.K. government allows cloning of human embryos for R&D purposes in disease treatments, but does not permit cloning of a person. This creates a question whether it will be possible to prevent human cloning if research continues. Development of possible cures for diseases is worth the risk of potential unethical application of cloning human embryos. This is a major factor hampering market growth to a significant extent, and the trend is expected to continue going ahead.

Some Key Highlights From the Report

  • In March 2020, Agilent Technology announced the launch of three new microarrays for prenatal and postnatal research. The microarray includes updated clinically relevant content from respected databases. Progression of next-generation sequencing is uncovering new gene-disease associations and databases are rapidly evolving to include these discoveries.
  • Carrier screening is a type of genetic test that can provide insights as to whether a patient carries a gene for genetic disorders. These patients display no symptoms but may be at risk of transferring it to their children. Carrier screening can be done before pregnancy, and it gives people a wide range of options and more time to make decisions.
  • Microarray analysis is done on a pregnant patient with one or more major structural abnormalities that were identified by ultrasonographic examination and is undergoing invasive prenatal diagnosis. Microarray test can replace the need for fetal karyotype. Microarray segment revenue is expected to register a rapid growth rate during the forecast period owing to increasing number of pregnant women seeking to gain insights into the prospects of having children and possibilities of genetic disorders.
  • Structural chromosomal abnormality can occur accidentally when the fetus is at early development stage. Mother’s age and certain environmental factors play a crucial role in genetic errors. Prenatal testing and screening can be done to examine chromosomal abnormalities. Chromosomal abnormalities can lead to disease, miscarriage, problem in growth or Down Syndrome.
  • North America accounted for largest revenue share in 2020 due to increase in number of IVF procedures, adoption of genomic techniques, and ongoing trend of replacement of traditional genomic technologies with advanced techniques. Presence of key market players in the region is also driving market revenue growth.
  • Key players in the market include Illumina, Inc., Agilent Technologies, Inc., PerkinElmer, Inc., Quest Diagnostics, Thermo Fisher Scientific Inc., Fulgent Genetics, Inc., Centogene AG, Myriad Genetics, Inc., Qiagen N.V., and OPKO Health, Inc.

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Emergen Research has segmented the global reproductive genetics market on the basis of product type, procedure type, technology, application, and region:

  • Product Type Outlook (Revenue, USD Billion; 2018–2028)
    • Laboratory Developed Tests (LDT)
    • Kits
    • Reagents and Consumables
  • Procedure Type Outlook (Revenue, USD Billion; 2018–2028)
    • Pre-Natal Screening
    • Pre-Implantation Genetic Testing
    • Infertility Genetic Testing
    • Carrier Screening
  • Technology Outlook (Revenue, USD Billion; 2018–2028)
    • Next-Generation Sequencing (NGS)
    • Microarray
    • Polymerase Chain Reaction (PCR)
    • In-Situ Hybridization (ISH)
  • Application Outlook (Revenue, USD Billion; 2018–2028)
    • Single Gene Disorder
    • Aneuploidy
    • Structural Chromosomal Abnormality
    • Others

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  • Regional Outlook (Revenue, USD Billion; 2018–2028)
    • North America
      1. U.S.
      2. Canada
      3. Mexico
    • Europe
      1. Germany
      2. U.K.
      3. France
      4. Spain
      5. BENELUX
      6. Rest of Europe
    • Asia Pacific
      1. China
      2. India
      3. Japan
      4. South Korea
      5. Rest of APAC
    • Latin America
      1. Brazil
      2. Rest of LATAM
    • Middle East & Africa
      1. Saudi Arabia
      2. UAE
      3. Israel
      4. Rest Of MEA

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