Newborn and Prenatal Genetic Testing Market, by Technology (Massively Parallel Sequencing, Array-based Technologies, Traditional Sanger Sequencing, Amplicon-based Sequencing, NGS Technology), by Application (Genome Analysis, Inborn Errors of Metabolism, Preterm Birth Risk Detection, Screening and Detection of Disease Mutations, Prenatal Breast Cancer Diagnosis) and, by End User (Research and Academic Institutes, Hospitals and Clinics, Commercial Laboratories, Other End Users): Opportunity Analysis and Industry Forecast, 2023-2032

An Overview

The report covers a study of by technology, by application, by end user. Region wise, the Newborn and prenatal genetic testing market trends are analyzed across North America, Europe, Asia-Pacific, and LAMEA. North America includes the U.S., Canada, and Mexico. Europe includes Germany, France, the UK, Italy, and rest of Europe. Asia-Pacific includes China, India, Japan, South Korea, and rest of Asia-Pacific. LAMEA includes Latin America, Middle East, and Africa. Moreover, the study covers quantitative analysis for Newborn and prenatal genetic testing market from 2023 to 2032. The CAGR is calculated from 2024 to 2032, considering all the micro- and macro-economic factors, which impact the growth of the Newborn and prenatal genetic testing market. In addition, the study includes various parameters such as market dynamics (drivers, restraints, and opportunities), parent/peer market analysis, value chain analysis, pricing analysis, Porter’s five force analysis, top player positioning in the base year, and impact of government regulations on the market, which impact the market growth.

Key companies identified in the report are Canon Medical Systems Corporation, Thermo Fisher Scientific, Illumina, Inc., Agilent Technologies, Sequenom, Inc., QIAGEN, Laboratory Corporation of America, PerkinElmer, Inc., Eurofins Scientific, NeuMoDx Molecular, Inc.

Key insights of Newborn and prenatal genetic testing market report

• The report includes in-depth analysis of different segments and provides market estimations between 2024 to 2032.

• This study presents the analytical depiction of the Newborn and prenatal genetic testing market with the current trends and future estimations to determine the imminent investment pockets

• The report includes the factors responsible for the market growth.

• The forecast period of the market is analyzed from 2024 to 2032 to highlight the Newborn and prenatal genetic testing market growth scenario.

• The report offers information related to key drivers, restraints, challenges, and opportunities with detailed analysis of the market size and share.

• Porter’s five forces model illustrates the potency of buyers & sellers, which is estimated to assist the market players to adopt effective strategies.

• The key market players are profiled to gain an understanding of the strategies adopted by them.

• This report provides a detailed analysis of the current trends and future estimations from 2024 to 2032, which helps to identify the prevailing market opportunities.

• The report provides detailed profiles for leading market players.

• The companies profiled include company overview, operating business segments, business overview, product portfolio, and recent developments.

  Newborn and Prenatal Genetic Testing Market, by Technology Report Highlights

Aspects	Details
By Technology	Massively Parallel Sequencing Array-based Technologies Traditional Sanger Sequencing Amplicon-based Sequencing NGS Technology
By Application	Genome Analysis Inborn Errors of Metabolism Preterm Birth Risk Detection Screening and Detection of Disease Mutations Prenatal Breast Cancer Diagnosis
By End User	Research and Academic Institutes Hospitals and Clinics Commercial Laboratories Other End Users
By Region	North America  (U.S., Canada, Mexico) Europe  (France, Germany, Italy, Spain, UK, Russia, Rest of Europe) Asia-Pacific  (China, Japan, India, South Korea, Australia, Thailand, Malaysia, Indonesia, Rest of Asia-Pacific) LAMEA  (Brazil, South Africa, Saudi Arabia, UAE, Argentina, Rest of LAMEA)
Key Market Players	Thermo Fisher Scientific Inc., QIAGEN, Eurofins Scientific, Canon Medical Systems Corporation, Laboratory Corporation of America, PerkinElmer, Sequenom, NeuMoDx Molecular, Agilent Technologies, Illumina

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