Monthly Archives: June 2020

As a Black woman descended from enslaved people, I often see ads for DNA ancestry kits that promise they will connect me to my roots, and I feel sorely tempted. Where in Africa were my ancestors stolen from? What languages did they speak, what beliefs did they hold? Could I somehow recover even the tiniest little piece of those identities stolen so long ago?

It is not a yearning exclusive to the Black community by any means, considering the various populations across the globe that have been forced from their ancestral lands and/or had their heritage and culture forcibly suppressed throughout the ages, but it is particularly common to the Black community. While I dont have hard statistics, from personal experience and anecdotal evidence I do feel that at-home DNA kits have been targeting Black consumers on the ancestry front more and more, realizing the particular allure their claims have for the many descendants of enslaved ancestors stolen from their homelands and purposefully stripped of their identitiestheir beliefs, their families, even their names. Ive started hearing more friends and family talking about using at-home DNA kits; I see more and more Black actors in DNA kit advertisements; at a Juneteenth celebration I attended one speaker openly encouraged the practice, enthusiastically sharing her own results.

I understand the yearning. I feel it myself and I know both sides of the coinI know exactly the sense of place and heritage Im missing on my fathers side because I have it on my mothers. While my fathers ancestry is full of questions and a surname that once belonged to a white man who owned my forebears, my mother is Irish, born and raised in a small town on the same land her family has farmed for generations. I spent most of my childhood summers there, exploring the dilapidated farmhouse that started off as a one-room stone cottage predating the Irish Potato Famine, hearing about how (for reasons I have never uncovered) my ancestors fared better when the blight came than several other nearby tenant farmers, who, so the story goes, would rummage through our garbage heap in search of turnip peels.

There is a sense of belonging and legacy in knowing a place like that, in being able to go to exactly where your ancestors lived and died, to sit in the shade of a tree you know a forebear planted. It is a privilege so widespread in some communities they have little notion of its specialness, or how many people have had that privilege stolen from them, sometimes several times over.

The prospect of being able to reclaim some of that privilege through genetic ancestry testing is hugely alluring. Unfortunately, it is also too good to be true, a promise that cannot really be kept, a stack of half-truths and statistical guesswork presented under a false veneer of certainty.

Consumer genetics companies sell us all a narrativea narrative of ourselves, of science certified self-discovery. Its a very tempting narrative, and theres now a multi-billion dollar industry that indicates they have gotten very good at selling it.

Most of these companies really sell three different thingsancestry, health information, and genealogy (i.e. connecting family trees)and sell them as if all three are equally accurate and scientifically backed. This is absolutely false. If connecting relatives and flagging genetic alleles of potential medical concern is like going outside and seeing what the weather is like, attempting to trace ones ethnicity and ancestral heritage via genomics is a lot more like looking at the tail end of a 30-day forecast. Theres a scientific basis to the projection at some level, but also significant room for error and, in the case of ancestry testing, lots of suppositions at play that can never be fully verified.

Theres been some reportage in the past few years regarding how DNA kit consumers have actually seen their ancestry results shift enormously as companies revamp their predictive models, but not nearly enough discussion of what that means, and exactly what it says about the half-truths and misconceptions on which this hugely profitable sector of the genomics industry is based.

Sure, companies lie through their teeth in advertising all the time, but theres something particularly disgraceful and infuriating about building an entire business around the impossible promise of revealing the truth, so lets break it down.

No matter how tempting the find your heritage message may be, or how adept DNA testing kit companies have gotten at pushing it, the thing that always stops me from succumbing to the siren song is a memory of a single PowerPoint slide from a Genetics course I took in college.

Theres a concept known as gene flow that refers to the transfer of genetic variation between different populations, and on that particular slide was a maxim so popular its often abbreviated: One migrant per generation is enough to conserve gene flow between populations, or OMPG. In other words, if there is any interbreeding at all between two groups, they are not going to diverge in any genetically distinguishable way. To apply this to the big picture, all human beings are 99.9% identical, and the variation in that remaining 0.1% really doesnt break down in a way that will tell you much about an individuals ancestral origins since our species, generally speaking, has long had a propensity for moving around and procreating with other human populations encountered along the way.

At this point, you might be wondering what ancestry DNA tests are actually testing, then, and how exactly they generate all those impressively specific percentages and spiffy graphs they give you in your results. The answer to that involves a whole lot of statistical calculations and banking on frequencies.

Heres a quick, hugely simplified run-down: there are regions within the human genome known as single nucleotide polymorphisms, or SNPs (snips). These are basically hotspots for genetic variation, places where its particularly common for random mutation to lead to one nucleotide being swapped out for anothera C to a T, for examplein a way that usually has no impact on an individuals health or development but is from there passed down through the generations (unless, of course, another mutation occurs somewhere down the line). SNPs are, in other words, silent mutations, but they are the lifeblood of ancestry testing because having a lot of SNPs in common suggests shared ancestry. The more SNPs in common, the more recently individuals likely shared a common ancestor. As for what a lot means in this context, of the 3.2 billion nucleotide base pairs in a human genome, some DNA ancestry tests analyze half a million or more SNPs.

As described earlier, there arent specific Somalian or Nigerian or Irish or Italian genes to look for in the DNA itself. What these companies do is take known reference populations to identify SNPs and patterns of SNPs that are particularly prevalent within particular ethnic groups and then analyze a customers DNA for the presence of these.

So, where do these known reference genomes come from and how can we all be so sure these people accurately know their ancestry dating back hundreds of years when the rest of us are being marketed kits to figure that out? The answer is we dont know, and these companies are incredibly tight-lipped about the whole thing.

I tried clicking around the 23andMe website for a while and eventually came to a very long, graph-filled page about the companys state-of-the-art geographic ancestry analysis which quickly boasts about the 14,000 people with known ancestry providing the basis for their analysis. The page then spends several thousand words giving an introductory genomics lesson that manages to not address how their analysis actually works at all, or why anyone should actually put any stock in the results it spits out. When the foundational reference data-set is brought up again, it is described as including genotypes from 14,437 people who were chosen to reflect populations that existed before transcontinental travel and migration were common (at least 500 years ago), which really, if anything, just begs more questions instead of providing any meaningful answers.

On the one hand, if you really believe in the unparalleled integrity of large corporations, you could make the case that such obfuscation is necessary to protect valuable trade secrets and there is nothing more to it than that. On the other, there is room to suspect between the handwaving and the support pages with fine print disclaimers like predicting inheritance is not an exact science that the secrecy might also have something to do with not wanting potential customers to cotton on to the fact that theyre selling a service that is one part science and two parts snake oil. Regardless, theres a distinct irony to having a whole industry built on the assumed accuracy of a known ancestry reference pool that most frequently promotes its product with ads about people thinking they know their heritage and discovering they were wrong.

Genetic testing isnt fundamentally evil or bad. There is a long list of privacy and ethical concerns surrounding the practice that have worryingly not yet been addressed in any meaningful way, but there are a number of legitimate applications for genetic testing that have the potential to do a lot of good if regulated appropriately. I, myself, have taken a particular kind of genetic test before and found it helpful. I deal with depression, and when trying to find a medication that was a good fit, my psychiatrist at the time suggested I do pharmacogenomics testing, or drug-gene testing, which specifically looks at your genes for variations known to be correlated with limited efficacy or experiencing side effects from a range of medications. My results indicated that the mechanism of action at work in many common antidepressants would be likely ineffective in my case, so the psychiatrist ended up prescribing a relatively new drug that worked differently. It ended up being a good fit for me. Odds are she would have suggested something else if I hadnt done the testing, and I ultimately think the test was worth it.

Genetic testing is a powerful tool, and only growing more so as our understanding of genetics evolves and methods become more and more sophisticated. But genetic testing is not all-powerful. There are certain things it cannot really tell us, not because we need bigger data sets or are still waiting on crucial breakthroughs, but because the shoe just doesnt fit, and it never really will.

Heres the thing about race, ethnicity, and culture: its not genetic. Yes, when you look at things like skin color and hair texture, there are connections, but its a Venn diagram with limited overlap. Thats not to say that race, ethnicity, and culture are somehow not real or not important. They are all very real and incredibly important. They just are not ultimately geneticalthough sometimes genetic-adjacent, if you will.

Were clear upfront that DNA is not identity. DNA is not culture, Robin Smith, the head of 23andMes Ancestry Division told STAT News for an article published last year, although clearly not the companys marketing department. Like other DNA ancestry kit companies, it rakes in millions of new customers every year with the allure of discover who you really are, not well send you a guess of who we think you might be based off of contested hypotheses and dodgy methodologies, then sell your genetic data to third parties for hundreds of millions of dollars because somehow people might not be as interested in forking over $100 or so when presented with the second option.

There are a lot of stories out theresome heartwarming, others heartbreakingabout DNA kit results completely reshaping a persons sense of self and family history. Now, if the results tell you that youre positive for a BRCA1 mutation or you have a long-lost cousin or your uncle is actually your dadthats all relatively straightforward, cut-and-dry genomics, and unless a lab technician processed your tube of spit wrong somehow, the findings are almost certainly accurate. But ancestry is a different matter. If you want to do a DNA ancestry kit as a bit of a lark or out of idle curiosity, thats one thing, but know that whatever results come back are just guesses, and can never be anything more.

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Don't Fall for the Impossible Promise of DNA Ancestry Kits - Pajiba

DetailsCategory: DNA RNA and CellsPublished on Tuesday, 23 June 2020 13:17Hits: 270

Century Therapeutics Canada will develop induced pluripotent Stem Cell (iPSC)-derived allogeneic immune cell therapies against glioblastoma (GBM)

PHILADELPHIA, PA, USA I June 23, 2020 ICentury Therapeutics today announced its acquisition of Empirica Therapeutics to leverage its iPSC-derived allogeneic cell therapies against glioblastoma (GBM).

We are pleased to welcome the Empirica team to the Century family. Their deep expertise and unique capabilities will allow us to accelerate efforts to develop iPSC derived immune effector cell products designed to treat and potentially cure brain cancer, said Lalo Flores, PhD, Chief Executive Officer of Century Therapeutics. GBM is a particularly aggressive, often treatment-resistant form of adult brain cancer with an average survival time of under two years. Together, we are in a stronger position to develop potentially curative cell therapies for this devastating disease.

Empirica Therapeutics was founded by Dr. Sheila Singh, MD, PhD, Professor of Surgery and Biochemistry and chief pediatric neurosurgeon at McMaster Childrens Hospital, and Dr. Jason Moffat, PhD, Professor of Molecular Genetics at the University of Toronto and an expert in functional genomics and gene-editing platforms. The companys science is based on a powerful integrative multi-omics platform, combined with its unique patient-derived, therapy-adapted models of recurrent GBM, that has led to the discovery and validation of novel brain tumor targets. Empiricas cutting edge preclinical models of recurrent GBM, have demonstrated the potential of CAR-T cell therapy in GBM, as published in a May 2020 Cell Stem Cell paper.

Our team is excited to become part of Century Therapeutics, whose iPSC-derived allogeneic cell therapies show immense potential for treating solid as well as hematologic malignancies, said Dr. Singh. Dr. Singh served as Empiricas CEO after co-founding the company with Chief Scientific Officer Dr. Moffat. We look forward to combining our unique patient-based cancer models with Centurys platform to create promising treatments for the patients who need them most, Singh said.

Janelle Anderson, PhD, Chief Strategy Officer at Century Therapeutics, shepherded the deal forming the subsidiary, which will be known as Century Therapeutics Canada and based in Hamilton, Ontario. Financial terms of the deal have not been disclosed.

About Century Therapeutics

Century Therapeutics is harnessing the power of stem cells to develop curative cell therapy products for cancer that overcome the limitations of first-generation cell therapies. Our genetically engineered, universal iPSC-derived immune effector cell products (iNK, iT) are designed to specifically target hematologic and solid tumor cancers. Our commitment to developing off-the-shelf cell therapies will expand patient access and provides an unparalleled opportunity to advance the course of cancer care. Century was launched in 2019 by founding investor Versant Ventures in partnership with Fujifilm and Leaps by Bayer. For more information, please visit http://www.centurytx.com.

About Glioblastoma (GBM)

Glioblastoma (GBM) is one of the most common types of primary brain tumor in adults and is almost uniformly lethal, with less than 5% of patients living beyond five years. GBM has an incidence rate of 3 per 100,000 people annually in the United States of America. The standard of care for GBM consists of tumor resection following by chemotherapy and radiation. Despite aggressive multimodal treatment, almost all patients experience relapse 7-9 months post-diagnosis and median survival has not extended beyond 16-20 months over the past decade. Recent studies suggest that the primary GBM tumor evolves significantly during the course of therapy and presents itself as a much more aggressive tumor at the time of recurrence. The treatment-resistant nature of GBM to standard therapies provides compelling motivation for developing novel treatment approaches.

SOURCE: Century Therapeutics

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Century Therapeutics Announces Acquisition of Empirica Therapeutics | DNA RNA and Cells | News Channels - PipelineReview.com

Personalized cancer test developer ArcherDX is walking away from plans to take itself public and into the arms of genetic testing company Invitae.

Earlier this month, ArcherDX announced it was filing for a $100 million Nasdaq IPObut instead it will reap a deal worth $1.4 billion, counting upfront cash, Invitae shares and future milestone payments. The two companies plan to integrate their genomics, tumor profiling and liquid biopsy technologies through one, overarching service.

"From the beginning, Invitae's goal has been to aggregate the world's genetic tests into a single platform in service of our mission to bring comprehensive genetic information into mainstream medicine. Today, we take another major step forward in that effort, Invitae co-founder and CEO Sean George said in a statement.

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The transaction begins with $325 million in cash plus 30 million shares of Invitae common stock; an additional 27 million shares are linked to milestones. The move has been approved by the boards of both companies and is expected to close within several months, the companies said.

To help carry the acquisition, Invitae has set up a strategic financing with over $400 million in commitments from investors, led by Perceptive Advisors. Invitae has agreed to sell $275 million of stock in a private placement at $16.85 a share, supported by Casdin Capital, Deerfield Management, Driehaus Capital Management, Farallon, PBM Capital, Redmile Group, Rock Springs Capital, Soleus Capital and an unnamed institutional investor.

RELATED: ArcherDX expands co-marketing, in vitro diagnostics partnerships with Illumina

Invitae has also secured a credit facility for up to $200 million with Perceptive Credit Opportunities Funds. Following the deals announcement, Invitaes stock rose nearly 50% from about $18 to over $26 a share.

We are thrilled to unite with Invitae to form the leading hub for precision oncology, diagnostics, therapy optimization and monitoring, with an opportunity to accelerate both patient care and shareholder value," said ArcherDXs co-founder and CEO Jason Myers.

ArcherDX currently counts over 325 unique products in its research services catalog and is developing in vitro cancer diagnostics with FDA submissions slated for later this year. The companys Stratafide DX and Personalized Cancer Monitoring efforts have both received breakthrough device designations from the agency.

ArcherDX also recently launched separate collaborations with AstraZeneca and Bristol Myers Squibb to apply its minimal residual disease assays to the drugmakers clinical cancer research.

RELATED: Invitae to buy DNA-counseling chatbot developer Clear Genetics for $50M

Together, the two companies aim to offer research and clinical trial support to biopharma companies as well as biomarker identification and companion diagnostic development while providing test reports, consultations and genetic counseling through Invitaes central laboratory.

"Integrating all aspects of cancer genetics can transform care for patients and the flexibility that comes from both centralized and decentralized capabilities will uniquely position Invitae to meet the needs of customers worldwide," said George. "By joining together, we will unite world-class capabilities in the hands of a talented team with complementary expertise and strong brands in service of a shared goal to improve healthcare for patients."

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ArcherDX drops IPO plans in favor of a $1.4B takeover by Invitae - FierceBiotech

Global DNA and RNA Sample Preparation Market: Trends Estimates High Demand by 2027

DNA and RNA Sample Preparation Market report 2020, discusses various factors driving or restraining the market, which will help the future market to grow with promising CAGR. The DNA and RNA Sample Preparation Market research Reports offers an extensive collection of reports on different markets covering crucial details. The report studies the competitive environment of the DNA and RNA Sample Preparation Market is based on company profiles and their efforts on increasing product value and production.

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The final report will add the analysis of the Impact of Covid-19 in this report DNA and RNA Sample Preparation industry.

Adapting to the recent novel COVID-19 pandemic, the impact of the COVID-19 pandemic on the global DNA and RNA Sample Preparation market is included in the present report. The influence of the novel coronavirus pandemic on the growth of the DNA and RNA Sample Preparation market is analyzed and depicted in the report.

Some of the companies competing in the DNA and RNA Sample Preparation market are: Agilent Technologies, Becton, Dickinson and Company, Bio-Rad Laboratories Inc., DiaSorin S.p.A., F. Hoffmann-La Roche, Illumina, PerkinElmer, QIAGEN, Sigma Aldrich Corp., Tecan Group AG ., and Thermo Fisher Scientific

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The report scrutinizes different business approaches and frameworks that pave the way for success in businesses. The report used Porters five techniques for analyzing the DNA and RNA Sample Preparation Market; it also offers the examination of the global market. To make the report more potent and easy to understand, it consists of info graphics and diagrams. Furthermore, it has different policies and development plans which are presented in summary. It analyzes the technical barriers, other issues, and cost-effectiveness affecting the market.

Global DNA and RNA Sample Preparation Market Research Report 2020 carries in-depth case studies on the various countries which are involved in the DNA and RNA Sample Preparation market. The report is segmented according to usage wherever applicable and the report offers all this information for all major countries and associations. It offers an analysis of the technical barriers, other issues, and cost-effectiveness affecting the market. Important contents analyzed and discussed in the report include market size, operation situation, and current & future development trends of the market, market segments, business development, and consumption tendencies. Moreover, the report includes the list of major companies/competitors and their competition data that helps the user to determine their current position in the market and take corrective measures to maintain or increase their share holds.

What questions does the DNA and RNA Sample Preparation market report answer pertaining to the regional reach of the industry

The report claims to split the regional scope of the DNA and RNA Sample Preparation market into North America, Europe, Asia-Pacific, South America & Middle East and Africa. Which among these regions has been touted to amass the largest market share over the anticipated duration

How do the sales figures look at present How does the sales scenario look for the future

Considering the present scenario, how much revenue will each region attain by the end of the forecast period

How much is the market share that each of these regions has accumulated presently

How much is the growth rate that each topography will depict over the predicted timeline

The scope of the Report:

The report segments the global DNA and RNA Sample Preparation market on the basis of application, type, service, technology, and region. Each chapter under this segmentation allows readers to grasp the nitty-gritties of the market. A magnified look at the segment-based analysis is aimed at giving the readers a closer look at the opportunities and threats in the market. It also address political scenarios that are expected to impact the market in both small and big ways.The report on the global DNA and RNA Sample Preparation market examines changing regulatory scenario to make accurate projections about potential investments. It also evaluates the risk for new entrants and the intensity of the competitive rivalry.

Reasons for Read this Report

This report provides pin-point analysis for changing competitive dynamics

It provides a forward looking perspective on different factors driving or restraining market growth

It provides a six-year forecast assessed on the basis of how the market is predicted to grow

It helps in understanding the key product segments and their future

It provides pin point analysis of changing competition dynamics and keeps you ahead of competitors

It helps in making informed business decisions by having complete insights of market and by making in-depth analysis of market segments

TABLE OF CONTENT:

Chapter 1: DNA and RNA Sample Preparation Market Overview

Chapter 2: Global Economic Impact on Industry

Chapter 3: DNA and RNA Sample Preparation 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: DNA and RNA Sample Preparation Market Effect Factors Analysis

Chapter 12: Global DNA and RNA Sample Preparation Market Forecast to 2027

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COVID19 Impact- Global DNA and RNA Sample Preparation Market Recent Industry Developments and Growth Strategies Adopted by Top Key Players Agilent...

Tennis world number one Novak Djokovic has been tested positive for coronavirus, joining a slew of other infected players who took part in his Adria Tour exhibition tournament in the Balkans.

"Novak Djokovic tested positive for a virus COVID-19," read a statement from his staff. "He is not showing any symptoms," it added.

Djokovic's wife Jelena also tested positive while the results of their children are negative, the statement read.Everything we did in the past month we did with a pure heart and sincere intentions, the statement reads.

I am extremely sorry for each individual case of infection.

The other tennis stars who have been tested positive are Grigor Dimitrov, Borna Coric, and Viktor Troicki

The tournament, which also had top names such as Dominic Thiem and Alexander Zverev, was held in Belgrade, and Zadar and the players were also pictured playing basketball and dancing together without following social distancing protocols, Reuters reported.

As for Zverev, the German tennis star on Monday confirmed that he and his team have tested negative for coronavirus.

"I have just received the news that my team and I have tested negative for COVID-19. I deeply apologize to anyone that I have potentially put at risk by playing this tour. I will proceed to follow the self-isolating guidelines advised by our doctors. As an added precaution, my team and I will continue with regular testing. I wish everyone who has tested positive a speedy recovery. Stay safe," Zverev wrote on Twitter.

The ATP and WTA Tours, which were suspended in March due to the pandemic, are set to resume in August with the US Open and French Open beginning on August 31 and September 27, respectively.

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Novak Djokovic tests positive for COVID-19, joins list of infected tennis players who appeared in Adria Tour - DNA India

Global DNA and Gene Chips Market: Trends Estimates High Demand by 2027

The DNA and Gene Chips Market 2020 report includes the market strategy, market orientation, expert opinion and knowledgeable information. The DNA and Gene Chips Industry Report is an in-depth study analyzing the current state of the DNA and Gene Chips Market. It provides a brief overview of the market focusing on definitions, classifications, product specifications, manufacturing processes, cost structures, market segmentation, end-use applications and industry chain analysis. The study on DNA and Gene Chips Market provides analysis of market covering the industry trends, recent developments in the market and competitive landscape.

It takes into account the CAGR, value, volume, revenue, production, consumption, sales, manufacturing cost, prices, and other key factors related to the global DNA and Gene Chips market. All findings and data on the global DNA and Gene Chips market provided in the report are calculated, gathered, and verified using advanced and reliable primary and secondary research sources. The regional analysis offered in the report will help you to identify key opportunities of the global DNA and Gene Chips market available in different regions and countries.

The final report will add the analysis of the Impact of Covid-19 in this report DNA and Gene Chips industry.

Some of The Companies Competing in The DNA and Gene Chips Market are: Bio MrieuxSA, Thermo Fisher Scientific Inc., Savyon Diagnostics, Agilent Technologies, Applied Micro Arrays Illumina Inc., Toshiba Hokuto Electronics Corporation, TOSHIBA Perkin Elmer Inc., Oxford Gene Technology, Arrayit Corporation, MYcroarray Macrogen Inc., Greiner Bio One, Asper Biotech, CapitalBio Corporation, and Microarrays Inc.

Get a Sample Copy of the [emailprotected] https://www.reportsandmarkets.com/sample-request/covid-19-impact-on-global-dna-and-gene-chips-market-size-status-and-forecast-2020-2026?utm_source=coleofduty&utm_medium=24

The report scrutinizes different business approaches and frameworks that pave the way for success in businesses. The report used Porters five techniques for analyzing the DNA and Gene Chips Market; it also offers the examination of the global market. To make the report more potent and easy to understand, it consists of info graphics and diagrams. Furthermore, it has different policies and improvement plans which are presented in summary. It analyzes the technical barriers, other issues, and cost-effectiveness affecting the market.

Global DNA and Gene Chips Market Research Report 2020 carries in-depth case studies on the various countries which are involved in the DNA and Gene Chips market. The report is segmented according to usage wherever applicable and the report offers all this information for all major countries and associations. It offers an analysis of the technical barriers, other issues, and cost-effectiveness affecting the market. Important contents analyzed and discussed in the report include market size, operation situation, and current & future development trends of the market, market segments, business development, and consumption tendencies. Moreover, the report includes the list of major companies/competitors and their competition data that helps the user to determine their current position in the market and take corrective measures to maintain or increase their share holds.

What questions does the DNA and Gene Chips market report answer pertaining to the regional reach of the industry?

The report claims to split the regional scope of the DNA and Gene Chips market into North America, Europe, Asia-Pacific, South America & Middle East and Africa. Which among these regions has been touted to amass the largest market share over the anticipated duration

How do the sales figures look at present how does the sales scenario look for the future?

Considering the present scenario, how much revenue will each region attain by the end of the forecast period?

How much is the market share that each of these regions has accumulated presently

How much is the growth rate that each topography will depict over the predicted timeline

A short overview of the DNA and Gene Chips market scope:

Global market remuneration

Overall projected growth rate

Industry trends

Competitive scope

Product range

Application landscape

Supplier analysis

Marketing channel trends Now and later

Sales channel evaluation

Market Competition Trend

Market Concentration Rate

Reasons to Read this Report

This report provides pin-point analysis for changing competitive dynamics

It provides a forward looking perspective on different factors driving or restraining market growth

It provides a six-year forecast assessed on the basis of how the market is predicted to grow

It helps in understanding the key product segments and their future

It provides pin point analysis of changing competition dynamics and keeps you ahead of competitors

It helps in making informed business decisions by having complete insights of market and by making in-depth analysis of market segments

TABLE OF CONTENT:

Chapter 1:DNA and Gene Chips Market Overview

Chapter 2: Global Economic Impact on Industry

Chapter 3:DNA and Gene Chips 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: DNA and Gene Chips Market Effect Factors Analysis

Chapter 12: GlobalDNA and Gene Chips Market Forecast to 2027

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About Us:

Reports And Markets is part of the Algoro Research Consultants Pvt. Ltd. and offers premium progressive statistical surveying, market research reports, analysis & forecast data for industries and governments around the globe. Are you mastering your market? Do you know what the market potential is for your product, who the market players are and what the growth forecast is? We offer standard global, regional or country specific market research studies for almost every market you can imagine.

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Sanjay Jain

Manager Partner Relations & International Marketing

http://www.reportsandmarkets.com

Ph: +1-352-353-0818 (US)

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Research on DNA and Gene Chips Market (impact of COVID-19) with Top Players: Bio MrieuxSA, Thermo Fisher Scientific Inc., Savyon Diagnostics, Agilent...