Global Preimplantation Genetic Screening Market Trends, Business Overview, Industry Growth and Forecast to 2022-2028
The application of preimplantation genetic screening is also increasing for the detection of single-gene disorder in people. According to the article published by the YourGenome, the single-gene disorder is a very rare condition represented by the mutated version of the gene responsible for the disorder. An estimation of around 1% of the global population is affected by a single-gene disorder. Furthermore, the application of preimplantation genetic screening is also increasing for several other purposes, including the detection of human leukocytes, structural chromosome abnormalities, X-linked disorders, and gender identity before birth as it offers several benefits, such as less uncertainty, improved embryo selection, gender selection during fertilization, prevention of various abnormal genetic transmissions, optimized chance of getting pregnant, and identification of fertility treatment.
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• The market number available for - 2021-2028
• Base year- 2021
• Forecast period- 2022-2028
• Segment Covered-
o By Technology
o By Application
• Regions Covered-
o North America
o Rest of the World
• Competitive Landscape- Thermo Fisher Scientific Inc., Illumina Inc., Agilent Technologies Inc., PerklinElmer Inc., and Abbott, among others.
Key questions addressed by the report
• What is the market growth rate?
• Which segment and region dominate the market in the base year?
• Which segment and region will project the fastest growth in the market?
• How has COVID-19 impacted the market?
o Deviation from the pre-COVID-19 forecast
o Most affected region and segment
• Who is the leader in the market?
• How players are addressing challenges to sustain growth?
• Where is the investment opportunity?
A full report of Global Preimplantation Genetic Screening Market is available at:
Global Preimplantation Genetic Screening Market Report by Segment
• Next-Generation Sequencing (NGS)
• Polymerase Chain Reaction (PCR)
• Fluorescence In Situ Hybridization (FISH)
• Comparative Genomic Hybridization (CGH)
• Single Nucleotide Polymorphism (SNP)
• Single Gene Disorder
• Structural Chromosome Abnormalities
• X-Linked Disorder
• Human Leukocyte
• Gender Identification
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