▶ 調査レポート

遺伝子検査の世界市場:タイプ別(保因者検査、診断検査、新生児スクリーニング、予測的検査・発症前診断、出生前検査、ニュートリゲノミクスによる検査)、疾病別(アルツハイマー病、がん、嚢胞性繊維症、鎌状赤血球貧血、デュシェンヌ型筋ジストロフィー、地中海貧血症、ハンチントン舞踏病、特定の疾病、その他)、技術別、地域別分析

• 英文タイトル:Global Genetic Testing Market - Segmented by Treatment Type, Diseases, Technology and Geography - Growth, Trends and Forecasts (2018 - 2023)

Mordor Intelligenceが調査・発行した産業分析レポートです。遺伝子検査の世界市場:タイプ別(保因者検査、診断検査、新生児スクリーニング、予測的検査・発症前診断、出生前検査、ニュートリゲノミクスによる検査)、疾病別(アルツハイマー病、がん、嚢胞性繊維症、鎌状赤血球貧血、デュシェンヌ型筋ジストロフィー、地中海貧血症、ハンチントン舞踏病、特定の疾病、その他)、技術別、地域別分析 / Global Genetic Testing Market - Segmented by Treatment Type, Diseases, Technology and Geography - Growth, Trends and Forecasts (2018 - 2023) / B-MOR-040832資料のイメージです。• レポートコード:B-MOR-040832
• 出版社/出版日:Mordor Intelligence / 2018年2月
• レポート形態:英文、PDF、120ページ
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レポート概要
本資料は、遺伝子検査の世界市場について調べ、遺伝子検査の世界規模、市場動向、市場環境、タイプ別(保因者検査、診断検査、新生児スクリーニング、予測的検査・発症前診断、出生前検査、ニュートリゲノミクスによる検査)分析、疾病別(アルツハイマー病、がん、嚢胞性繊維症、鎌状赤血球貧血、デュシェンヌ型筋ジストロフィー、地中海貧血症、ハンチントン舞踏病、特定の疾病、その他)分析、技術別分析、アメリカ市場規模、ヨーロッパ市場規模、アジア市場規模、日本市場規模、中国市場規模、企業の競争環境、関連企業情報などをまとめた調査レポートです。
・イントロダクション
・エグゼクティブサマリー
・遺伝子検査の世界市場インサイト
・遺伝子検査の世界市場環境
・遺伝子検査の世界市場動向
・遺伝子検査の世界市場規模
・遺伝子検査の世界市場規模:タイプ別(保因者検査、診断検査、新生児スクリーニング、予測的検査・発症前診断、出生前検査、ニュートリゲノミクスによる検査)
・遺伝子検査の世界市場規模:疾病別(アルツハイマー病、がん、嚢胞性繊維症、鎌状赤血球貧血、デュシェンヌ型筋ジストロフィー、地中海貧血症、ハンチントン舞踏病、特定の疾病、その他)
・遺伝子検査の世界市場規模:技術別
・遺伝子検査の世界市場:地域別市場規模・分析
・遺伝子検査の北米市場規模・予測
・遺伝子検査のアメリカ市場規模・予測
・遺伝子検査のヨーロッパ市場規模・予測
・遺伝子検査のアジア市場規模・予測
・遺伝子検査の日本市場規模・予測
・遺伝子検査の中国市場規模・予測
・遺伝子検査のインド市場規模・予測
・遺伝子検査の韓国市場規模・予測
・関連企業情報・競争状況

As of 2017, the global genetic testing market was valued at USD 9,367.0 million and is expected to record a CAGR of around 10.4% during 2018-2023 (the forecast period). In 2017, the North American genetic testing segment of the market studied accounted for the highest revenue and Asia-Pacific is expected to register the highest CAGR of 12.6% over the forecast period

Growing Demand for Personalized Medicine

Personalized medicine, where tailored therapy is made available to patients with an understanding of the molecular basis of diseases, has become popular over the recent years. Genetic testing and genome sequencing are two of the most important tools that are used to understand the molecular basis of a disease. European countries are screened for several genetic diseases, as an early detection of these diseases can prevent the onset of symptoms, or minimize the severity of the disease. Genetic testing for cancer diagnosis can indicate the predisposition of the disease in the gene, before its actual manifestation. This type of diagnostic technique enables a person to take precautionary steps, and avoid possible risks in the future.

Social and Ethical Implications of Genetic Testing

Insurance is an important asset to people. The fear of discrimination by insurance companies discourages people from undertaking genetic tests, which is a restraining factor for the market growth. The expensive nature of genetic tests affects the market, adversely. At times, the payments made by individuals are not reimbursed through insurance, thus, affecting the pockets of these patients. The high-import duty by the government on genetic tests kits also acts as a barrier to the market growth.

North America to Dominate the Market

The genetic testing market is segmented by treatment type, diseases, technology, and geography. By geography, the market has been segmented into North America, Europe, Asia-Pacific, the Middle East & Africa, and South America.
Owing to the presence of well-established healthcare facilities and new discoveries in the field of genetic markers, North America dominates the genetic testing market. The Asia-Pacific market is expected to register the highest CAGR, as government and private firms are making significant investments in the healthcare industry. Over the last couple of years, to invest in the Japanese market, several mergers, acquisitions, and collaborations between companies have taken place.

Key Developments in the Market

• September 2017: Myriad Launched riskScore to enhance the hereditary cancer test myRisk. riskScore determines the risk of women to get breast cancer by analyzing their genome.
• July 2017: Admera Health Partners collaborates with Helix to Launch Genetic Tests to Assess the Risk of Inherited High Cholesterol, Sudden Cardiac Death, and Inherited Diabetes

Major Players: 23 AND ME INC., ABBOTT MOLECULAR INC, ARIOSA DIAGNOSTICS INC, BIOCARTIS SA, CEPHEID, ILLUMINA INC, LUMINEX CORPORATION, SEQUENOM INC, MYRIAD GENETICS, TRANSGENOMIC INC. amongst others.

Reasons to Purchase This Report

• Market analysis for the Global Genetic testing Market, with region-specific assessments and competition analysis on the global and regional scale
• Analyzing various market perspectives, with the help of Porter’s five forces analysis
• The treatment type that is expected to dominate the market
• Regions that are expected to witness fastest growth during the forecast period
• Identify the latest developments, market shares, and strategies employed by the major market players
• 3 months analyst support, along with the Market Estimate sheet (in excel)

Customization of the Report

• This report can be customized to meet your requirements. Please connect with our analyst, who will ensure you get a report that suits your needs.

レポート目次

1. Introduction
1.1 Market Definition
2. Research Methodology
3. Executive Summary
4. Key Inferences
5. Market Overview
5.1 Current Market Scenario
5.2 Porter’s Five Forces Analysis
5.2.1 Bargaining Power of Suppliers
5.2.2 Bargaining Power of Consumers
5.2.3 Threats of New Entrants
5.2.4 Threat of Substitute Product And Services
5.2.5 Competitive Rivalry Within the Industry
6. Drivers, Restraints, Opportunities And Challenges Analysis (DROC)
6.1 Market Drivers
6.1.1 Increasing Emphasis on Early Disease Detection and Prevention
6.1.2 Growing Demand for Personalized Medicine
6.1.3 Increasing Application of Genetic Testing in Oncology
6.2 Market Restraints
6.2.1 High Costs of Genetic Testing
6.2.2 Social and Ethical Implications of Genetic Testing
6.3 Opportunities
6.4 Key Challenges
7. Market Segmentation
7.1 Segmentation-By Type
7.1.1 Carrier Testing
7.1.2 Diagnostic Testing
7.1.3 Newborn Screening
7.1.4 Predictive and Presymptomatic Testing
7.1.5 Prenatal Testing
7.1.6 Nutrigenomic Testing
7.2 Segmentation-By Disease
7.2.1 Alzheimer’s Diseases
7.2.2 Cancer
7.2.3 Cystic Fibrosis
7.2.4 Sickle Cell Anemia
7.2.5 Duchenne Muscular Dystrophy
7.2.6 Thalassemias
7.2.7 Huntington’s Disease
7.2.8 Special Diseases
7.2.9 Others
7.3 Segmentation-By Technology
7.3.1 Cytogenetic Testing
7.3.2 Biochemical Testing
7.3.3 Molecular Testing
7.4 Segmentation-By Geography
7.4.1 North America
7.4.1.1 US
7.4.1.2 Canada
7.4.1.3 Mexico
7.4.2 Europe
7.4.2.1 France
7.4.2.2 Germany
7.4.2.3 UK
7.4.2.4 Italy
7.4.2.5 Spain
7.4.2.6 Rest Of Europe (RoE)
7.4.3 Asia-Pacific
7.4.3.1 China
7.4.3.2 Japan
7.4.3.3 India
7.4.3.4 Australia & New Zealand
7.4.3.5 South Korea
7.4.3.6 Rest Of Asia-Pacific
7.4.4 Middle East & Africa
7.4.4.1 GCC
7.4.4.2 South Africa
7.4.4.3 Rest Of the Middle East & Africa
7.4.5 South America
7.4.5.1 Brazil
7.4.5.2 Argentina
7.4.5.3 Rest Of South America
8. Competitive Landscape
8.1 Mergers & Acquisition Analysis
8.2 Agreements, Collaborations, and Partnerships
8.3 New Products Launches
9. Key Players
9.1 23 and Me Inc.
9.2 Abbott Molecular Inc.
9.3 Ariosa Diagnostics Inc.
9.4 Biocartis SA
9.5 Cepheid
9.6 Illumina Inc.
9.7 Luminex Corporation
9.8 Sequenom Inc.
9.9 Myriad Genetics
9.10 Transgenomic Inc.
10. Future of the Market