Rare Disease Genetic Testing Market

Rare Disease Genetic Testing Market Size, Share, Growth Analysis, By Disease Type(Neurological Disease, Immunological Disorders), By Technology(Next-Generation Sequencing (NGS), Array Technology), By Specialty(Molecular Genetic Tests, Chromosomal Genetic Tests), By End-Use(Research Laboratories & CROs, Hospitals & Clinics), By Regional Scope(North America, Europe) - Industry Forecast 2024-2031


Report ID: UCMIG35H2211 | Region: Global | Published Date: Upcoming |
Pages: 165 | Tables: 55 | Figures: 60

Rare Disease Genetic Testing Market Insights

Market Overview:

The global rare disease genetic testing market demonstrated a significant value of USD 887.79 million in 2022, indicating its substantial presence in the Health Care industry. Forecasts suggest that the market is poised to experience substantial growth, with a projected compound annual growth rate (CAGR) of 14.30% between 2023 and 2030. This anticipated expansion reflects the increasing demand for accurate and efficient genetic testing methods to diagnose and manage rare diseases. Factors such as advancements in genetic sequencing technologies, growing awareness among Health Care professionals, and rising investment in research and development initiatives are expected to drive the market's growth over the forecast period.

Rare Disease Genetic Testing Market, Forecast & Y-O-Y Growth Rate, 2020 - 2028
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This report is being written to illustrate the market opportunity by region and by segments, indicating opportunity areas for the vendors to tap upon. To estimate the opportunity, it was very important to understand the current market scenario and the way it will grow in future.

Production and consumption patterns are being carefully compared to forecast the market. Other factors considered to forecast the market are the growth of the adjacent market, revenue growth of the key market vendors, scenario-based analysis, and market segment growth.

The market size was determined by estimating the market through a top-down and bottom-up approach, which was further validated with industry interviews. Considering the nature of the market we derived the Biotechnology by segment aggregation, the contribution of the Biotechnology in Pharmaceuticals, Biotechnology & Life Sciences and vendor share.

To determine the growth of the market factors such as drivers, trends, restraints, and opportunities were identified, and the impact of these factors was analyzed to determine the market growth. To understand the market growth in detail, we have analyzed the year-on-year growth of the market. Also, historic growth rates were compared to determine growth patterns.

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FAQs

The market for Rare Disease Genetic Testing was estimated to be valued at US$ XX Mn in 2021.

The Rare Disease Genetic Testing Market is estimated to grow at a CAGR of XX% by 2028.

The Rare Disease Genetic Testing Market is segmented on the basis of Disease Type, Technology, Specialty, End-Use, Regional Scope.

Based on region, the Rare Disease Genetic Testing Market is segmented into North America, Europe, Asia Pacific, Middle East & Africa and Latin America.

The key players operating in the Rare Disease Genetic Testing Market are Quest Diagnostics Inc., Centogene N.V., Invitae Corp., 3billion, Inc., Arup Laboratories, Eurofins Scientific, Strand Life Sciences, Ambry Genetics, Perkin Elmer, Inc., Realm IDX, Inc., Macrogen, Inc., Baylor Genetics, Color Genomics, Inc., Health Network Laboratories, PreventionGenetics, Progenity, Inc., Coopersurgical, Inc., Fulgent Genetics Inc., Myriad Genetics, Inc., Laboratory Corporation of America Holdings, Opko Health, Inc., Artemis DNA.

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Rare Disease Genetic Testing Market

Product ID: UCMIG35H2211

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