Human Genetics Market 2022 Share, Size, Trend, SWOT Analysis and Forecast to 2030
Human genetics is the broad field of studying human
inheritance and comprises sub-sections such as cytogenetics, molecular
genetics, genetic counseling, clinical genetics, and others. It helps to
understand gene functionalities and the consequences of abnormalities in them.
Through human genetics, the human genome is studied to diagnose genetic
disorders and provide related treatment much more efficiently.
The
global human genetics market is expected to have a market value of USD
60,821.20 million by 2030.The
growth of human genetics is driven by the growing adoption of genetic testing.
However, high cost of genetic testing is likely to restrain the market
growth.
Major Key Players:
MRFR recognizes Human Genetics Market Players are— Myriad Genetics
(US), Synlab Group (Germany), Eurofins Megalab S.A
(Spain), Biomarker Technology (US), Echevarne Laboratory
(Spain), Elabscience Biotechnology Inc (US), NIMGenetics
(Spain), Sistemas Genómicos (Spain), FullGenomics (Spain), GENinCode
(UK), Atrys Health (Spain), Genyca (Spain), Igenomix
(India), Genologica (Spain), Bode Technology Group Inc (US).
Key Findings of the Study
US accounted for the largest share of the global human
genetics market due to the increasing demand for genetic testing by the
population are driving the market in the region. For instance, according to
Healthline Media (US), in October 2019, United HealthCare Services, Inc. (US),
the largest health insurance company in the US, started providing insurance
coverage for multi-panel genetic testing. According to the National Institutes
of Health (NIH), in July 2022, over 77,000 genetic tests are currently used in
the US, and more are under development.
Regional
Analysis
The global human molecular genetics
market, based on region, has been divided into US, Canada, UK, Germany, Spain, Japan, others.
The human genetics market in the
US benefits from a high healthcare expenditure, increasing demand for genetic
testing by the population, and high public awareness regarding early detection
of diseases and preventive care. Moreover, the availability of reimbursements
in the US for genetic tests further improves market growth in the country. For
instance, in October 2019, United HealthCare Services, Inc. (US), the largest
health insurance company in the US, started providing insurance coverage for
multi-panel genetic testing. According to the National Institutes of Health
(NIH), in July 2022, over 77,000 genetic tests are currently used in the US,
and more are under development.
Public-funded genetic testing in
Canada is highly restricted and is only available to a select few who fall into
certain criteria, such as a family history of cancer and early onset of cancer.
Additionally, people in Canada who want their genetic testing done can opt for
direct-to-consumer genetic tests such as color and invitae. Results from these
tests can then be consulted with genetic counselors. Furthermore, there are
human genetics programs to test patients with genetic disorders across Canada.
For instance, the Hereditary Cancer Program is based in British Columbia,
Canada, conducting genetic counseling and tests to detect hereditary cancer.
Clinically directed genetic
testing has been available for several decades in the NHS for predictive
testing for family members and molecular genetic investigation of a clinical
presentation. Genomic health data in the UK is generated in three major areas,
including large-scale research programs, the healthcare system, and purchasing
of direct-to-consumer genetic testing. Moreover, the rise in the number of
initiatives undertaken by the public as well as private organizations is
further aiding the market growth. For instance, in April 2022, GEN inCode UK
Limited announced its collaboration with Royal Brompton and Harefield hospitals
(RB&H) for providing cardiovascular disease clinical genetic testing and
reporting. In August 2022, DnaNudge announced the completion of its Series A
investment round of USD 60 million led by Ventura Capital
The rising prevalence of genetic
disorders, cancer, increasing awareness and acceptance regarding personalized
medicines, and growing focus on R&D activities contribute to the country's
growth. As per the data published by Global Cancer Observatory in March 2022,
cancer accounted for 628,516 new cases and 252,065 deaths in Germany in 2022.
In addition, the government is implementing a number of favorable and
collaborative policies to incorporate genetic testing into the healthcare
system and provide insurance reimbursements to citizens, which, in turn, is
driving the market growth.
Segmentation
The global human genetics market
is segmented into application, end user and region. The application segment is
further segmented into wellness & E-commerce, preventive
medicine, diagnostic & treatment. The diagnostic & treatment segment
is further sub-segmented into oncology, cardiology, assisted reproduction,
neurology, gynecology, others. The neurology segment is further
sub-segmented into neuropediatric, others. The test segment is further
segmented into NIPT, carrier testing, pharmacogenomic testing, karyotype
testing, thrombophilia testing, septin 9 biomarker
testing, NGS, others. The NGS segment is further sub-segmented into
oncology, cardiology, others.
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