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市場調査レポート
商品コード
1439025
アジア太平洋の希少疾患遺伝子検査市場:分析と予測(2023年~2033年)Asia-Pacific Rare Disease Genetic Testing Market: Analysis and Forecast, 2023-2033 |
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カスタマイズ可能
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アジア太平洋の希少疾患遺伝子検査市場:分析と予測(2023年~2033年) |
出版日: 2024年02月29日
発行: BIS Research
ページ情報: 英文 104 Pages
納期: 1~5営業日
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主要市場統計 | |
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予測期間 | 2023年~2033年 |
2023年の評価 | 5億8,000万米ドル |
2033年予測 | 24億米ドル |
CAGR | 15.25% |
アジア太平洋の希少疾患遺伝子検査市場は、2023年に5億8,000万米ドルとなりました。
同市場は、2033年には24億米ドルに達すると予測され、予測期間の2023年~2033年のCAGRは15.25%になると予測されています。全ゲノムシーケンシング(WGS)や全エクソームシーケンシング(WES)のような先進技術は、それぞれ個人の全遺伝コード(ゲノム)または特定のタンパク質コード領域(エクソーム)を解析します。これらの技術は、希少疾患に関連する遺伝的変異、突然変異、異常の検出に役立ちます。
アジア太平洋の希少疾患遺伝子検査市場は、様々な要因によって著しい成長を遂げています。認知度の向上、遺伝子検査技術の進歩、医療費の増加が市場拡大に寄与しています。さらに、この地域の人口の多さと多様な遺伝子プロファイルは、遺伝子検査プロバイダーに大きな機会をもたらしています。ヘルスケアインフラの改善と遺伝子検査サービスへのアクセス拡大を目指す政府の取り組みは、市場成長をさらに促進します。さらに、ヘルスケア機関、研究機関、業界関係者の協力により、この地域特有のニーズに合わせた革新的な遺伝子検査ソリューションの開発と導入が促進されています。精密医療と個別化ヘルスケアへの注目が高まる中、APACの希少疾患遺伝子検査市場は、当面、継続的な拡大と革新が見込まれます。
当レポートでは、アジア太平洋の希少疾患遺伝子検査市場について調査し、市場の概要とともに、疾患タイプ別、技術別、国別の動向、および市場に参入する企業のプロファイルなどを提供しています。
The Asia Pacific Rare Disease Genetic Testing Market Expected to Reach $2.40 Billion by 2033
Introduction to Asia-Pacific Rare Disease Genetic Testing Market
KEY MARKET STATISTICS | |
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Forecast Period | 2023 - 2033 |
2023 Evaluation | $0.58 Billion |
2033 Forecast | $2.40 Billion |
CAGR | 15.25% |
The Asia-Pacific rare disease genetic testing market was valued at $0.58 billion in 2023 and is anticipated to reach $2.40 billion by 2033, witnessing a CAGR of 15.25% during the forecast period 2023-2033. Advanced technologies like whole-genome sequencing (WGS) and whole-exome sequencing (WES) analyze an individual's entire genetic code (genome) or specific protein-coding regions (exome), respectively. They aid in detecting genetic variations, mutations, or abnormalities linked to rare diseases.
Market Introduction
The Asia-Pacific (APAC) rare disease genetic testing market is witnessing notable growth driven by various factors. Increased awareness, advancements in genetic testing technologies, and rising healthcare expenditure contribute to market expansion. Moreover, the region's large population base and diverse genetic profiles present significant opportunities for genetic testing providers. Government initiatives aimed at improving healthcare infrastructure and expanding access to genetic testing services further propel market growth. Additionally, collaborations between healthcare organizations, research institutions, and industry players facilitate the development and adoption of innovative genetic testing solutions tailored to the region's specific needs. With a growing focus on precision medicine and personalized healthcare, the APAC rare disease genetic testing market is poised for continued expansion and innovation in the foreseeable future.
Market Segmentation:
Segmentation 1: by Disease Type
Segmentation 2: by Technology
Segmentation 3: by Country
How Can This Report Add Value to an Organization?
Product/Innovation Strategy: The APAC rare disease genetic testing market has been extensively segmented based on various categories, such as disease type, technology, and country. This can help readers understand which segments account for the largest share and which are well-positioned to grow in the coming years.
Competitive Strategy: The APAC rare disease genetic testing market has numerous established players paving their way into providing tests, panels, and assays in the market. Key players in the global rare disease genetic testing market analyzed and profiled in the study involve established players offering various disease-specific panels and multiplex instruments.
Key Market Players and Competition Synopsis
The companies that are profiled have been selected based on inputs gathered from primary experts and analysing the company's coverage, product portfolio, its market penetration.
Some of the prominent names established in this market are:
Research Methodology