Category Archives: Genetics

SOPHiA GENETICS and the Spanish Lung Cancer Group Team Up to Explore the Predictive Potential of Multimodal Health Data in Resectable Stage IIIA…

February 9, 2021 medical

The collaboration with the Spanish Lung Cancer Group (Grupo Espaol de Cncer de Pulmn GECP), a Spanish cooperative group for the research on lung cancer, is to show the potential of SOPHiA Radiomics a groundbreaking application that analyzes medical images for research use put to use in an additional retrospective analysis of the data from the phase 2 NADIM clinical trial (NCT03081689) (the NADIM trial).

The NADIM trial, funded by Bristol-Myers Squibb and part of the European Union's Horizon 2020 research and innovation program, aimed to assess the antitumor activity and safety of neoadjuvant chemoimmunotherapy for resectable stage IIIA NSCLC. The important results recently published in TheLancet Oncology supported the addition of neoadjuvant nivolumab to platinum-based chemotherapy in patients with resectable stage IIIA NSCLC. This very aggressive type of cancer is unfortunately terminal in most patients with locally advanced staged disease; these results could therefore support a change of perception of locally advanced lung cancer as a potentially lethal disease to one that is curable.

Additional data are expected to be generated through the analysis of the radiology images of NADIM patients through the SOPHiA Radiomics Platform. These data will then be combined with clinical, biological, and genomics data, and multimodal machine learning models will be developed to predict response to neoadjuvant treatment, using baseline and pre-surgery data. The predictive analysis will also aim to stratify patient cohorts with regard to progression-free and overall survival.

"We are very happy to collaborate in this innovative and revolutionary project that opens the door to a new precision medicine. Certainly, this partnership will improve the knowledge relating to the treatment for this group of patients and will allow to approach the best prospects for curing early-stage non-small cell lung cancer (NSCLC)," said Dr. Mariano Provencio, Head of the Medical Oncology Department at Puerta de Hierro University Hospital in Madrid and lead investigator of the NADIM trial.

"We are very excited to apply our radiomics and multimodal analytics capabilities to such an important clinical question," said Prof. Thierry Colin, Vice-President of Radiomics Research at SOPHiA GENETICS. "In the Spanish Lung Cancer Group, we have found visionary partners that clearly see the promise of next-generation health data such as radiomics being married with tech-enabled solutions in artificial intelligence to generate entirely novel clinical insights for the benefit of oncology patients."

"Unlocking the synergistic potential of multimodal health data through artificial intelligence holds revolutionary promise for the future of personalized medicine in oncology and many other health conditions. We are inspired by the potential to positively impact on patients by supporting their care providers in predicting the best course of treatment," said Dr. Philippe Menu, Chief Medical Officer at SOPHiA GENETICS.

The NADIM trial involved 18 centers from the Spanish Lung Cancer Network that will contribute their data to the joint project.

Results from the additional analysis of NADIM trial data are expected to be available later this year.

About SOPHiA GENETICS

SOPHiA GENETICS is a health tech company democratizing Data-Driven Medicine to improve health outcomes and economics worldwide. By unlocking the power of new-generation health data for cancer and rare diseases management, the universal SOPHiA Platform allows clinical researchers to act with precision and confidence. The company's innovative approach enables an ever-expanding community of over 1,000 institutions to benefit from knowledge sharing, fostering a new era in healthcare. SOPHiA's achievement is recognized by the MIT Technology Review's "50 Smartest Companies".

More info: SOPHiAGENETICS.COM, follow @SOPHiAGENETICS on Twitter.

About the Spanish Lung Cancer Group

The SLCG is an independent, non-profit, cooperative group founded in 1991 to promote the study and research of lung cancer. The group is composed of 525 medical professionalsoncologists, thoracic surgery specialists, radiotherapists and basic researchersand unites 177 public and private centers across Spain.The group has treated over 37,000 patients in different studies and clinical trials, the results of which have been presented and published at national and international congresses and in leading medical journals.

More info: gecp.com, follow @gecp_org on Twitter.

SOPHIA GENETICS Media ContactSophie ReymondPR & Communications Manager [emailprotected]+41 79 863 11 10

SLCG ContactRita Perales [emailprotected] +34 670 24 70 50

SOURCE SOPHiA GENETICS

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SOPHiA GENETICS and the Spanish Lung Cancer Group Team Up to Explore the Predictive Potential of Multimodal Health Data in Resectable Stage IIIA...

Genetics

Science reveals genetic reasons behind different face shapes – Open Access Government

February 9, 2021 medical

The human face has endless ways of existing, this immense variation witnessed for centuries across ethnicities and continents, across gender and language barriers.

Despite this multitude of ways to have a face, the global cosmetic surgery industry is expected to hit $50.5 billion by 2027.

It is currently the age of The Instagram Face leading individuals to pursue a specific set of features, which celebrity makeup artist Colby Smith described as: an overly tan skin tone, a South Asian influence with the brows and eye shape, an African-American influence with the lips, a Caucasian influence with the nose, a cheek structure that is predominantly Native American and Middle Eastern.

Despite how multicultural this ideal face appears, it is dismissive of genetic difference. The faces that are extensively crafted to look like this, via surgery or filter, have a racial ambiguity that disowns any real affiliation to race. This in itself is a worrying sentiment, as darker skinned people across the world remain at risk of discrimination.

Researchers in this study wanted to understand the legacy of the faces we have today where did they come from? And what could those genes tell them about ancestral adaptions of the face?

Recently, UCL researchers found 32 gene regions that influenced features such as nose, lip, jaw, and brow shape. Nine of these regions were completely new discoveries, while the others validated genes with little prior evidence.

The team analysed data from more than 6,000 volunteers across Latin America. This study compared genetic information from the study participants with characteristics of their face shape, quantified with 59 measurements (distances, angles and ratios between set points) from photos of the participants faces in profile.

The international research team, led from UCL, Aix-Marseille University and The Open University, found that one of the genes appears to have been inherited from the Denisovans. They are an extinct group of ancient humans, who lived tens of thousands of years ago.

The team found that the gene, TBX15, which contributes to lip shape, was linked with genetic data found in the Denisovan people, providing a clue to the genes origin.

One of the newly discovered genes found in this study is VPS13B, which influenced nose pointiness the researchers also found that this gene affects nose structure in mice. This further suggests there is a link between mammal gene influences.

Co-corresponding author Dr Kaustubh Adhikari (UCL Genetics, Evolution & Environment and The Open University) commented: The face shape genes we found may have been the product of evolution as ancient humans evolved to adapt to their environments. Possibly, the version of the gene determining lip shape that was present in the Denisovans could have helped in body fat distribution to make them better suited to the cold climates of Central Asia, and was passed on to modern humans when the two groups met and interbred.

The Denisovans lived in central Asia, and other studies suggest they interbred with modern humans, as some of their DNA lives on in Pacific Islanders and Indigenous people of the Americas.

Co-first author Dr Pierre Faux (Aix-Marseille University) said: To our knowledge this is the first time that a version of a gene inherited from ancient humans is associated with a facial feature in modern humans.

In this case, it was only possible because we moved beyond Eurocentric research; modern-day Europeans do not carry any DNA from the Denisovans, but Native Americans do.

Co-corresponding author Dr Kaustubh Adhikari (UCL Genetics, Evolution & Environment and The Open University) said: The face shape genes we found may have been the product of evolution as ancient humans evolved to adapt to their environments. Possibly, the version of the gene determining lip shape that was present in the Denisovans could have helped in body fat distribution to make them better suited to the cold climates of Central Asia, and was passed on to modern humans when the two groups met and interbred.

Read the full study here.

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Science reveals genetic reasons behind different face shapes - Open Access Government

Genetics

Evenings with Genetics: Race and Genetics | BCM – Baylor College of Medicine News

February 5, 2021 medical

Do racial categories obscure our genetic similarities and differences? How do we quantify ancestry and is it important in precision medicine? This month, Baylor College of Medicine is hosting two Evenings with Genetics webinars to address these questions and other issues involving race and genetics.

The webinars will take place on Tuesday, Feb. 9, and Tuesday, Feb. 16, at 7 p.m. CST. Both sessions will address the role of race in genetic research and clinical care, as well as racial justice and bioethics in precision medicine.

This series focused on race and Black history is exciting and timely, said Dr. Debra Murray, assistant professor of molecular and human genetics at Baylor and co-organizer of the event. The invited speakers will bring to light several areas where genetics has been influenced by race. In order to pursue social justice, we must ensure science without bias. People with non-European ancestry should not be prevented from enjoying the promise of precision medicine.

The 15th anniversary of this series is the perfect opportunity to offer our community these discussions on the perception of race as we strive to ensure precision medicine is available to all, said Susan Fernbach, assistant professor of molecular and human genetics at Baylor and co-organizer of the event.

Panelists on Feb. 9 include Dr. Charmaine Royal, professor of African & African American studies, biology, global health and family medicine and community health at Duke University, Dr. Clayton Yates, professor in the Department of Biology and Center for Cancer Research at Tuskegee University, and Shawneequa Callier, associate professor in the Department of Clinical Research and Leadership at the George Washington University School of Medicine and Health Sciences.

Panelists on Feb. 16 include Dr. Rick Kittles, professor and director of the Division of Health Equities in the Department of Population Sciences at City of Hope, Dr. Charmita Hughes-Halbert, professor in the Department of Psychiatry and Behavioral Sciences at Medical University of South Carolina, and patient advocate J.H. Jones.

The program is free and open to the public, but registration is required. A Zoom link will be sent to all registered participants. For more information, call 713-798-8407 or visit the event registration pages for Feb. 9 and Feb. 16. Videos of both sessions will be available online here at a later date.

This event is sponsored by the Department of Molecular and Human Genetics, the Office of Diversity, Equity and Inclusion, the Human Genome Sequencing Center and Baylor Genetics.

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Evenings with Genetics: Race and Genetics | BCM - Baylor College of Medicine News

Genetics

What 23andMe’s filing to go public says about the big genetics business – STAT

February 5, 2021 medical

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What 23andMe's filing to go public says about the big genetics business - STAT

Genetics

From Ancestry to Genetics-Based Drug Development, Richard Branson Takes 23andMe Public – BioSpace

February 5, 2021 medical

Billionaire Sir Richard Branson believes in healthcare. This week he put more of his money where his mouth is by using his SPAC to take consumer DNAtesting company23andMepublic in a massive deal.

At Virgin, we try to partnerwith companies that can make a real difference in the world like healthcare companies...saidBransonin an interview.

The essentially reverse merger delivers $759 million to 23andMe and bumps up the companys value to $3.5 billion.Launched in2006,for most, it was a neat way to find out who youare, who your ancestors were, where they came from, and even your genetic predispositions that put you at higher risk for certain diseases.But the company has grownintoevenmore than that.

Ancestry and health have always been key components of the product but more and more the future is the health side. How is it that you can get your genetic information and really benefit from the Human Genomeand life a healthier life?saidCEOand co-founderAnne Wojcicki.

Its these exciting opportunities in the healthcare aspect that convinced Branson the company was ripe for his next big investment.

23andMe, for instance, just their drug development side could shorten the development of a new drug using allthe knowledge that theyve gained over the last twelve years by as much as 3 years which makes coming up with drugs that much quicker, said Branson.

Both Branson and Wojcicki personally contributed $25 million to the deal. Branson was also an early investor in the company, having contributed to 23andMes Series A.

23andMes first program,Move Forward, is now in humantrialswithpartnerGlaxoSmithKline.Theimmuno-oncologyprogram was GSKs, validated by 23andMes proprietary algorithm.Wojcicki was tightlippedfor nowon the timeline for any data.

If you think back on our mission statement, its about helping customers access, understand and benefit from the Human Genome. And the key thing that were doing right now is helping our customers benefit. Theyregoing to benefit in two ways. One is they are going to be empowered with information to help them live a healthier life. And second is on the therapeutic side. 23andMe is working hard to say how do we analyze all this data? How do weunderstand those genetics so we can develop very personalized therapeutics that could potentially cure diseases, saidWojcicki.

All data studied as part of the collaboration with GSK and all 23andMe research is from customers who opted-in to a separate research consent. Privacy is a majorconcern for consumers in todays data age.

Last January,Spanish pharma companyAlmirallin-licensed a bispecific monoclonal antibodyfrom 23andMethat blocksallmembers of the IL-36 cytokinesubfamily. Associated with multiple inflammatory diseases and dermatological conditions, Almirall is developing and commercializing the antibody for global use.

Window into the genetics behind equine reproduction grows ever wider, say researchers – Horsetalk

February 5, 2021 medical

The genetic origins behind reproductive traits are still far from clear, and this is especially so for horses, researchers say. Photo by Phinehas Adams

The knowledge of the reproductive architecture of horses on a genetic level is likely to grow considerably over the next few years, the authors of a just-published review predict.

The genetic origins behind reproductive traits are still far from clear, and this is especially so for horses.

Nora Laseca and her colleagues, writing in the journal Animals, said reproductive traits are complex and usually determined by multiple genes.

They also have low heritability, which makes them particularly sensitive to environmental and management factors, such as age, nutrition, training, temperature at mating, and breeding season.

By that reason, modeling reproductive traits from a genetic point of view is difficult, they wrote in their review of recent advances and studies analyzing genomic mechanisms affecting reproductive function in mares and stallions.

This is particularly important in equines, whose fertility is considerably lower than that observed in other domestic species, they said.

In addition, equine reproductive efficiency is limited by their own physiology, characterized by single births in almost all the foalings, seasonality in mares, long generation intervals delaying genetic improvement, and a lack of systematized collection of phenotypic information reproductive traits.

Nevertheless, a certain degree of genetic influence has been described and modelized from a quantitative viewpoint, in mares and stallions.

For instance, gestation length in mares is affected by maternal lineage or inbreeding, while changes in sperm traits are related to the genetic background of the individual, lineage and breed, as well as by the inbreeding value.

However, there are very few reports which describe the molecular mechanisms involved in such genetic influence or which detect the candidate genes involved in the biological processes.

The advent of genomics has led to the development of new approaches to genetic analysis in livestock, including the detection of specific mutations and other genetic issues.

However, their use in equines is still limited, probably due to the delay in the development of a reliable reference genome, in comparison with most livestock species, such as pigs or cattle, but also by a lack of reliable expected progeny differences and phenotypic values associated to the variations in fertility in the species.

Laseca and her colleagues noted that, although the use of genomic methods in horses has increased significantly over the past five years, studies focusing on reproductive traits remain few and far between.

There are even fewer which aim to dissect and quantify more accurately the influence of the genetic background and the environment in the expression of the observable traits, they noted.

Horse genomics is currently undergoing an exponential expansion, not least due to the adaptation of new genomic methodologies to the species, the existence of a new, accurate reference genome, and the exponential increase in the number of equines which have been genotyped.

It is, therefore, highly likely that our knowledge of the reproductive architecture of horses will grow considerably over the next few years.

However, large-scale datasets of reproductive phenotypes are still scarce in horses, probably due to the lack of availability of reliable reproductive phenotypes (particularly in mares).

Therefore, the development of new phenotypes to measure reproductive fitness more objectively and their systematic use by breeder associations are essential to allow a more in-depth study of the reproductive function in horses.

In addition, the search for candidate genes is a highly promising way to obtain a better understanding of the processes involved in horse fertility.

They not only can help to elucidate which physiological functions could be affected by a specific genotype, but also to predict which genotypes could be more affected by environmental challenges, and they can be integrated into breeding programs to detect, even at very young ages, the potential fertility (increased, normal, or decreased) of a given mare or stallion.

The authors said the lack of consistency observed in candidate genes associated with fertility detected in different breeds or populations of horses, (most of them detected by a single study) will be reduced only with an increase in the volume of evidence gathered.

In this sense, only 11 genes reviewed in their paper were detected by two or more studies, and only five were detected using more than one approach.

It was recently shown that combined genomic approaches in the same study can increase accuracy and reliability in detecting candidate genes. However, no combined studies have yet been reported in horses. Such combined approaches would constitute the best approach in our search for a better, more reliable understanding of genetic effects on horse fertility.

The review team comprised Laseca, Gabriel Anaya, Zahira Pea and Antonio Molina, with the University of Crdoba in Spain; and Yamila Pirosanto and Sebastin Demyda Peyrs, with the National University of La Plata and the Higher Council for Scientific and Technological Research, both in La Plata, Argentina.

Laseca, N.; Anaya, G.; Pea, Z.; Pirosanto, Y.; Molina, A.; Demyda Peyrs, S. Impaired Reproductive Function in Equines: From Genetics to Genomics. Animals 2021, 11, 393. https://doi.org/10.3390/ani11020393

The review, published under a Creative Commons License, can be read here.

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Window into the genetics behind equine reproduction grows ever wider, say researchers - Horsetalk

Genetics

Animal Genetics Market to Witness Robust Expansion by 2027 with Top Key players like Genus Plc, Hendrix Genetics, Ew Group Gmbh, Grimaud Groupe, Alta…

February 5, 2021 medical

Animal genetics refers to the branch of genetics that deals with the study of inheritance and gene variation in domestic and wild animals. This involves gene expression, animal breeding and physical genetic traits such as coat color, body structure, facial shape, and others which is entirely based on heredity. Animal genetics are used for DNA testing, genetic trait testing, and genetic disease training. The animal genetics market is anticipated to increase due to the rapid demand, consumption of animal proteins, and increase in urban population, which exhibits demand for meat products across the globe during the forecast period.

The global Animal Genetics Market size is expected to Expand at Significant CAGR of +6% during forecast period (2021-2027).

The report on the global Animal Genetics market is a complete overview of the market, covering various aspects product definition, segmentation based on various parameters, and the prevailing vendor landscape. It compiles in-depth information and research methodologies. It is also combined with relevant charts and tables to enable readers to get a better perspective of this global market.

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Top Key Players Profiled in this Report:

Genus Plc, Hendrix Genetics, Ew Group Gmbh, Grimaud Groupe, Alta Genetics, Inc., Crv Holding B.V., Neogen Corporation, Zoetis, Inc., Envigo (Harlan Laboratories, Inc.), Animal Genetics Inc., Vetgen.

This report provides a detailed and analytical look at the various companies that are working to achieve a high market share in the global Animal Genetics market. Data is provided for the top and fastest growing segments. This report implements a balanced mix of primary and secondary research methodologies for analysis. Markets are categorized according to key criteria. To this end, the report includes a section dedicated to the company profile. This report will help you identify your needs, discover problem areas, discover better opportunities, and help all your organizations primary leadership processes. You can ensure the performance of your public relations efforts and monitor customer objections to stay one step ahead and limit losses.

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Market Penetration:Comprehensive information on the product portfolios of the top players in the Animal Genetics market.

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Competitive Assessment: In-depth assessment of the market strategies, geographic and business segments of the leading players in the market.

Market Development:Comprehensive information about emerging markets. This report analyzes the market for various segments across geographies.

Market Diversification:Exhaustive information about new products, untapped geographies, recent developments, and investments in the Animal Genetics market.

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The report gathers the essential information including the new strategies for growth of the industry and the potential players of the global Animal Genetics Market. It enlists the topmost industry player dominating the market along with their contribution to the global market. The report also demonstrates the data in the form of graphs, tables, and figures along with the contacts details and sales of key market players in the global Animal Genetics Market.

Global Animal Genetics Market Segmentation:

Market Segmentation: By Type

Market Segmentation: By Application

For extensive comprehension of market dynamics, the Animal Genetics Market is bifurcated among various regions:

Years considered for this report:

Table of Contents

Global Animal Genetics Market Research Report 2021 2027

Chapter 1 Animal Genetics Market Overview

Chapter 2 Global Economic Impact on Industry

Chapter 3 Global Market Competition by Manufacturers

Chapter 4 Global Production, Revenue (Value) by Region

Chapter 5 Global Supply (Production), Consumption, Export, Import by Regions

Chapter 6 Global Production, Revenue (Value), Price Trend by Type

Chapter 7 Global Market Analysis by Application

Chapter 8 Manufacturing Cost Analysis

Chapter 9 Industrial Chain, Sourcing Strategy and Downstream Buyers

Chapter 10 Marketing Strategy Analysis, Distributors/Traders

Chapter 11 Market Effect Factors Analysis

Chapter 12 Global Animal Genetics Market Forecast

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Genetics

JK Agri Genetics reports standalone net loss of Rs 2.70 crore in the December 2020 quarter – Business Standard

February 5, 2021 medical

Sales rise 9.57% to Rs 34.47 crore

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First Published: Fri, February 05 2021. 17:52 IST

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JK Agri Genetics reports standalone net loss of Rs 2.70 crore in the December 2020 quarter - Business Standard

Genetics

Genetic Testing Market Analysis 2021 with Top Companies, Production, Consumption, Price and Growth Rate 23andMe, Abbott, Ambry, Genetics BGI KSU |…

February 5, 2021 medical

This market study on Genetic Testing Market covers the global and regional market with an in-depth breakdown of the inclusive growth prospects in the market. Also, it sheds light on the wide-ranging competitive landscape of the global Genetic Testing market. It defines about the recent innovations, applications and end users of the market.The report first introduces the market basics like definitions, classifications, applications, and industry chain overview, and then industry policies and plans, product specifications, manufacturing processes, cost structures, and so on.Global Genetic Testing market report lends a hand with businesses to thrive in the market by providing them with an array of insights about the market and the industry. Inputs from various industry experts, essential for the detailed market analysis, have been used very carefully to generate this finest market research report.

Genetic testing market is expected to gain market growth in the forecast period of 2021 to 2028. Data Bridge Market Research analyses the market to reach at an estimated value of 585.81 billion and grow at a CAGR of 11.85% in the above-mentioned forecast period. Increase in incidences of genetic disorders and cancer drives the genetic testing market.

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The major players who are leading the market throughout the globe are:

The Genetic Testing market report comprises of several market dynamics and estimations of the growth rate and the market value based on market dynamics and growth inducing factors. For generation of an excellent market research report, principal attributes such as highest level of spirit, practical solutions, dedicated research and analysis, innovation, talent solutions, integrated approaches, most advanced technology and commitment plays a key role. The report contains reviews about key players in the market, major collaborations, merger and acquisitions along with trending innovation and business policies. While preparing the winning Genetic Testing report, markets on the local, regional as well as global level are explored.

Genetic Testing Market Segmentation:

By Type (Predictive & Presymptomatic Testing, Carrier Testing, Prenatal & Newborn Testing, Diagnostic Testing, Pharmacogenomic Testing, Others)

By Technology (Cytogenetic Testing, Biochemical Testing, and Molecular Testing)

By Application (Cancer Diagnosis, Genetic Disease Diagnosis, Cardiovascular Disease Diagnosis, Others)

By Disease (Alzheimers Disease, Cancer, Cystic Fibrosis, Sickle Cell Anemia, Duchenne Muscular Dystrophy, Thalassemia, Huntingtons Disease, Rare Diseases, Other Diseases)

MAJOR TOC OF THE REPORT:-

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Competitive Landscape and Genetic TestingMarket Share Analysis

Genetic testing market competitive landscape provides details by competitor. Details included are company overview, company financials, revenue generated, market potential, investment in research and development, new market initiatives, global presence, production sites and facilities, production capacities, company strengths and weaknesses, product launch, product width and breadth, application dominance. The above data points provided are only related to the companies focus related to genetic testing market.

The major players covered in the genetic testing market report are 23andMe, Inc., Abbott., Ambry Genetics., BGI, Biocartis, BIO-HELIX, bioMrieux SA, Blueprint Genetics Oy, Cepheid., deCODE genetics, GeneDx, Inc., Exact Sciences Corp, HTG Molecular Diagnostics, Genomictree., Illumina, Inc, Invitae Corporation, Laboratory Corporation of America Holdings, Luminex Corporation., ICON plc, Myriad Genetics, Inc, Natera, Inc., Pacific Biosciences of California, Inc, Pathway Genomics, QIAGEN, Quest Diagnostics Incorporated, F. Hoffmann-La Roche Ltd and Siemens Healthcare Private Limited among other domestic and global players. Market share data is available for Global, North America, Europe, Asia-Pacific (APAC), Middle East and Africa (MEA) and South America separately. DBMR analysts understand competitive strengths and provide competitive analysis for each competitor separately.

Significant Highlights of the Report:

Centered Study on Strategy, Development & market Scenario

Global Top Companies Share Analysis in Genetic Testing Market

Achieve strategic insights on competitor information to develop powerful industry growth

Identify emerging players and create effective counter-strategies to cross the competitive edge

Identify crucial and various product types/distribution channel offering provided by major players for Genetic Testing market growth

To provide a more accurate market forecast, all our reports will be updated before delivery taking into account the effects of COVID-19.

Global Genetic Testing Market Scope and Market Size

Genetic testing market is segmented on the basis of type, technology, application, disease and product. The growth amongst these segments will help you analyse meagre growth segments in the industries, and provide the users with valuable market overview and market insights to help them in making strategic decisions for identification of core market applications.

Genetic Testing Market Country Level Analysis:

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Genetic Testing Market Analysis 2021 with Top Companies, Production, Consumption, Price and Growth Rate 23andMe, Abbott, Ambry, Genetics BGI KSU |...

Genetics