Page 2,711«..1020..2,7102,7112,7122,713..2,7202,730..»

Category Archives: Transhuman News

Roche Takes Control of Innovative DNA Test Maker Foundation Medicine

Posted: January 12, 2015 at 8:48 pm

A $1 billion deal for tests that can steer patients to the right drug.

The pharmaceutical giant Roche plans to spend $1 billion to acquire majority control of Foundation Medicine, a five-year old company that developed an innovative DNA test to match patients to specific cancer drugs.

We profiled Foundation in back in 2012 (see Foundation Medicine: Personalizing Cancer Drugs), highlighting how the spinout of the MIT-Harvard Broad Institute was one of the first to introduce tests to sequence the DNA of a tumor biopsy to pinpoint the exact mutations driving a persons tumor, and possibly steer treatment. At the time, we described Foundations pricey $5,800 cancer test, called FoundationOne, this way:

Foundations business model hinges on the convergence of three recent developments: a steep drop in the cost of decoding DNA, much new data about the genetics of cancer, and a growing effort by pharmaceutical companies to develop drugs that combat the specific DNA defects that prompt cells to become cancerous.

Foundation tried something new and important. But it turns out that its hard to make money in diagnostics, and the technology of DNA testing is developing and changing very quickly, too. All that helps explain why the company agreed to sell a little over half its shares to Roche, which sells more cancer drugs than anyone. As the New York Times says today:

Roche, which is the worlds largest seller of cancer drugs, said it would use some insights from that testing to develop drugs and better tailor them for specific groups of patients. In addition, Roche, which also has a huge diagnostics business, will sell Foundations tests outside the United States.

I think it just brings personalized health care in oncology to a new level, Daniel ODay, who runs Roches pharmaceutical business, said in an interview.

The Foundation deal appears to be the largest in a series of takeovers by Roche of innovative diagnostics firms. A few years back, Roche tried and failed to acquire Illumina, the sequencing machine company whose technology underlies the explosion in DNA research. But Roche is finding no shortage of companies that are willing to sell. During the last twelve months, it bought Ariosa, a prenatal testing company, as well as Genia Technologies, which Roche paid $350 million for, and Bina Technologies, which develops bioinformatics software.

Foundations test is used to analyze a tumor for several hundred cancer-linked genes. As we reported in 2013, an early and famous customer for this technology was Apple founder Steve Jobs (see Steve Jobs Left a Legacy on Personalized Medicine):

It turns out that Jobs was one of the first peopleand certainly the best-knownto try this kind of all-in genetic strategy to beat cancer. As recounted in Walter Isaacsons biography of the Apple CEO, Jobs spent $100,000 to learn the DNA sequence of his genome and that of the tumors killing him. Jobs was jumping between treatments and hoped DNA would provide clues about where to turn next.

Read the original post:
Roche Takes Control of Innovative DNA Test Maker Foundation Medicine

Posted in DNA | Comments Off on Roche Takes Control of Innovative DNA Test Maker Foundation Medicine

Animal DNA on the Go Seen for First Time

Posted: at 8:48 pm

A type of DNA for the first time has been observed moving from one cell to another in animals.

Genetic material called mightocondria convert energy from food into a form that can be used by cells. In the experiment, a tumor cell without mitrochondrial DNA formed tumors after pulling in DNA from normal cells.

Our findings overturn the dogma that genes of higher organisms are usually constrained within cells except during reproduction," Mike Berridge, a professor from the Malaghan Institute of Medical Research in New Zealand, said in a statement. "It may be that mitochondrial gene transfer between different cells is actually quite a common biological occurrence.

Berridge along with Jiri Neuzil from Griffith University in Queensland, Australia, led a team that examined breast cancer tumors in mice. Mitochondrial DNA was removed from cells, which then pulled replacement DNA from surrounding, normal mouse tissue.

The effect has been observed in the lab before, the researchers said, but not in an animal tumor.

The researchers initially thought the cells had adapted to grow without the mitochondrial DNA that had been removed. But after testing, the scientists discovered the cells did have mitochondrial DNA pulled from non-tumor cells.

The researches say the findings may help in understanding more about 200 diseases besides cancer that involve defective mitochondrial DNA. "It could also usher in a new field where synthetic mitochondrial DNA is custom-designed to replace defective genes," the researchers wrote.

If mitochondrial DNA sounds familiar, that may be because it's used in studying human ancestry. The genetic material is passed down only by one's mother, and has been instrumental in tracing a common human ancestor back to Africa 60-70,000 years ago.

The results were published in the journal Cell Metabolism.

View original post here:
Animal DNA on the Go Seen for First Time

Posted in DNA | Comments Off on Animal DNA on the Go Seen for First Time

23andMe Gives Pfizer DNA Data as Startup Seeks Growth

Posted: at 8:48 pm

Jan. 12 (Bloomberg) -- 23andMe Director of Business Development Emily Drabant Conley discusses her companys collaboration with Pfizer to help find new targets to treat disease and to design clinical trials. She speaks on "Bloomberg West." (Source: Bloomberg)

23andMe Inc., the genetic-testing startup backed by Google Inc. (GOOG), is sharing DNA data on about 650,000 individuals with Pfizer Inc. (PFE), to help find new targets to treat disease and to design clinical trials.

The collaboration with Pfizer is the broadest announced so far in 23andMes ambitious plan to become a repository for humanitys genetic makeup, and to turn data gathered from $99 saliva tests sold to consumers into multimillion-dollar deals with drugmakers.

The agreement unveiled today gives the U.S.s largest drugmaker access to anonymous, aggregated information from consumers who bought 23andMes test over the past seven years to learn about their own genetic histories. It includes only people who agreed to let their data be used in research. Pfizer and 23andMe declined to give the deals value.

Related: 23andme Aims to End FDA Standoff This Year After Public Shaming

The Silicon Valley startup, named for the 23 pairs of chromosomes in human cells, is betting its growing troves of genetic data will prove essential to drug companies, medical researchers and even health and wellness companies.

Even as it seeks to expand its consumer tests around the world, the company is repairing relations with the U.S. Food and Drug Administration. An agency ruling in late 2013 left 23andMe unable to sell health analyses from the saliva tests.

Anne Wojcicki, co-founder and chief executive officer of 23andMe Inc., speaks during a Bloomberg Television interview in San Francisco, California, on Oct. 9, 2014. Close

Anne Wojcicki, co-founder and chief executive officer of 23andMe Inc., speaks during a... Read More

Close

See more here:
23andMe Gives Pfizer DNA Data as Startup Seeks Growth

Posted in DNA | Comments Off on 23andMe Gives Pfizer DNA Data as Startup Seeks Growth

DNA Connect gets into Aerohive

Posted: at 8:48 pm

Aerohives architecture and cloud management platform will open up business opportunities for MSPs

Distributor, DNA Connect has added US-based Wi-Fi and cloud-managed mobile networking vendor, Aerohive Networks, to its portfolio.

Aerohive's mobility platform takes advantage of the cloud and a distributed architecture to provide intelligent, simplified and cost-effective networks.

DNA Connect executive director, Munsoor Khan, said Aerohives architecture and cloud management platform opens up a new line of business for managed service providers (MSP).

Were already seeing traction with MSPs offering customers a fixed monthly price per access point with the MSP managing everything in the cloud, Khan said.

The distributor is also investing in certifying its engineers to help conduct in-country certification training for the channel and users.

As a value-added distributor were looking for ways to help grow the Aerohive channel, Khan said. Were encouraging channel partners of all types - regardless of which wireless vendors they may be working with, to take a look at the Aerohive solution and to keep up with the market as it continues to move to cloud-based services.

Aerohive Networks country manager, Peter Davison, said its controller-less Wi-Fi architecture was growing in the market.

The contract was only signed just prior to the Christmas break, and its already yielding. Theyll springboard us to doubling our revenue within the next 18 months, Davison said.

The addition of Aerohive complements DNA's existing vendor line up such as Splunk, Huawei, Imperva and Ixia.

Read the original:
DNA Connect gets into Aerohive

Posted in DNA | Comments Off on DNA Connect gets into Aerohive

23andMe Teams With Big Pharma to Find Treatments Hidden in Our DNA

Posted: at 8:48 pm

On Monday, 23andMe announced it is sharing (anonymously) the DNA data it has collected on 650,000 individuals with pharmaceutical giant Pfizer. Sharing resources, the companies say, will help them figure out new ways to treat disease and to design clinical trials.

The terms of the deal were not disclosed publicly, but any good news is a step forward for the beleaguered startup. Since it launched in 2007, the Silicon Valley startup has built its business on analyzing DNA extracted from customers saliva to let them learn more about their ancestry, inherited traits, and risk factors for medical conditions. About 800,000 customers have signed up for 23andMes services over seven years, with two-thirds of them giving consent to let their personal test data be used in research.

Researchers hope to use 23andMes trove of genetic data to decipher connections between DNA and disease.

During those years, the company endured its share of controversy, culminating in a late-2013 clash with the U.S. Food and Drug Administration, which claimed 23andMe was in effect marketing a medical device without proper approvals. The FDA also contended the startup was slow in responding to agency inquiries, further souring their relationship.

The company dealt with the blow in part by selling its tests outside the U.S. And 23andMe CEO Anne Wojcicki recently told Bloomberg that the startup has been trying to repair its ties with the FDA. In May, the company began focusing its efforts on a new test limited to detecting a single genetic disorder, called Bloom syndrome, she said. The hope, according to Wojcicki, is that proceedings will move faster once this test is approved by the agency.

In the meantime, 23andMe appears to have figured out how to capitalize on the trove of personal test data it has already acquired. The anonymized collection of gene scans represents a huge sample of genetic profiles from which researchers hope to decipher connections between DNA and disease. The data appears to be valuable enough that Pfizer isnt the only big pharma company looking to dig further. Last week, according to Forbes, 23andMe inked a deal with Genentech worth $10 million up front, and up to $50 million if further milestones are reached.

With two big names already on their roster of clients, its likely that other major pharmaceutical companies will follow suit in hopes of leveling the competitive playing field. And in fact 23andMe has said it would announce a total of 10 similar deals with drugmakers and biotechnology companies this year. Its also likely, though, that collaborating with so many big pharmaceutical companies will bring renewed scrutiny from privacy advocates who have criticized the collection of so much highly personal data into one place.

But controversy is nothing new to 23andMe, and as its tests sit on the shelf, its understandable the company would look to capitalize on one of its most valuable assets. Leveraging its data has always been part of 23andMes business plan. If pharmaceutical companies are able to sift that data and uncover new treatments, that data could come to benefit us all.

Original post:
23andMe Teams With Big Pharma to Find Treatments Hidden in Our DNA

Posted in DNA | Comments Off on 23andMe Teams With Big Pharma to Find Treatments Hidden in Our DNA

Evaluating and ranking genome assemblers by Michael Barton – Video

Posted: at 8:47 pm


Evaluating and ranking genome assemblers by Michael Barton
Scientific results are shared as manuscripts which researchers read and interpret in their own work. Based in the field of genomics, this talk will show how ...

By: Docker

Read the original post:
Evaluating and ranking genome assemblers by Michael Barton - Video

Posted in Genome | Comments Off on Evaluating and ranking genome assemblers by Michael Barton – Video

Genomics: The Slow Revolution

Posted: at 8:47 pm

Contributed By:

Michelle Leis

OPB | Jan. 12, 2015 12:06 p.m. | Updated: Jan. 12, 2015 1:41 p.m.

In 2003, the first human genome wassequenced through the collaborative effort of 20 research centers. It cost nearly $3billion.

Almost 12 years later, the cost ofsequencing has come down faster than Moores law. We can now sequence an entire genome for $2,000 to $3,ooo in a fraction of the time it took to sequence that first humangenome.

In the first part of a new series on genomics, we examine the ways in which genetic data is used to personalize medicine, and take a look at whats being done in the clinical setting. Specifically, well address how this technology has changedwhat we know about cancer and discuss some of the limitations of what we can accomplish through genomeanalysis.

GUESTS:

In the next part of our series, well look into some of the legal and ethical concerns surrounding geneticresearch.

Rose E. Tucker Charitable Trust

James F. and Marion L. Miller Foundation

View original post here:
Genomics: The Slow Revolution

Posted in Genome | Comments Off on Genomics: The Slow Revolution

Convergence of regulatory, reimbursement forces threaten patient care, experts say

Posted: at 8:47 pm

The Association for Molecular Pathology (AMP), the premier global, non-profit organization serving molecular testing professionals, announced the release of an important white paper addressing the consequences of regulatory and reimbursement forces directed against molecular diagnostic testing that threaten patient care. The paper, titled, "A Molecular Diagnostic Perfect Storm: The Convergence of Regulatory & Reimbursement Forces that Threaten Patient Access to Innovations in Genomic Medicine" is now available online at http://bit.ly/1yGlghJ.

"The breakthroughs made possible by mapping the human genome -- a multi-billion dollar project that took more than a decade to complete -- are being threatened by government regulations, which in turn are threatening patient access to truly revolutionary treatments," said Victoria M. Pratt, PhD, Indiana University School of Medicine, active AMP Member, and lead author of the paper. "We hope that this manuscript further enlightens regulatory and reimbursement stakeholders about the storm brewing in Washington that could dismantle the development and coverage of important molecular diagnostic tests."

Medical professionals in universities, cancer centers, clinical laboratories, and pharmaceutical/manufacturing companies across the country have honored the public trust in the Human Genome Project by developing hundreds of innovative diagnostic tests and therapies that are advancing modern medicine in ways that would have been impossible without this breakthrough. By eliminating the barriers outlined in "The Perfect Storm" paper, genome-based research will continue to play a critical role in the development of more powerful tools to treat complex diseases such as cancer, diabetes, and cardiovascular disease.

Threats stemming from efforts by the U.S. Food and Drug Administration (FDA) and the Centers for Medicare and Medicaid Services (CMS), the two federal agencies that oversee molecular diagnostic testing, are the cause of this "Perfect Storm."

The FDA's new policies will effectively reformulate existing medical device regulations and consider medical professionals as manufacturers which will impose substantially new and duplicative requirements on clinical laboratories and hospitals. Meanwhile, CMS, who runs Medicare, the nation's largest insurer and whose actions are frequently mimicked in the private sector, has taken a heavy handed approach in denying coverage or reducing payment for several medically necessary molecular pathology tests. Unfortunately, health care providers -- those developing and delivering innovative diagnostic tests -along with patients, who are the ultimate intended beneficiaries, are caught in the middle.

"AMP is addressing the consequences of this gathering perfect storm of regulatory and reimbursement challenges directed against molecular diagnostic testing with recommendations designed to preserve patient access to these essential medical services" said AMP President, Janina Longtine, MD. "We are greatly concerned that these forces are coalescing to bring about consolidation of laboratory testing, to the detriment of local testing. This would have far-reaching negative effects on the healthcare system. As such, AMP is committed to working with the regulatory and reimbursement bodies to find a resolution that optimizes patient safety and offers access to important medical tests."

Story Source:

The above story is based on materials provided by Association for Molecular Pathology. Note: Materials may be edited for content and length.

Original post:
Convergence of regulatory, reimbursement forces threaten patient care, experts say

Posted in Genome | Comments Off on Convergence of regulatory, reimbursement forces threaten patient care, experts say

Personal Genome Diagnostics, Inc. And Human Longevity, Inc …

Posted: at 8:47 pm

BALTIMORE and LA JOLLA, Calif., Jan. 12, 2015 /PRNewswire/ --Personal Genome Diagnostics, Inc. (PGDx), a provider of advanced cancer genome analysis and testing services, and Human Longevity, Inc. (HLI), the human health information technology and health care company, today announced that HLI will have access to PGDx's cancer genomics solutions to expand its analysis of cancer genomes, including CancerSelect, PlasmaSelect, CancerXome, METDetect and CancerComplete. HLI has also licensed the PGDx Enterprise Solution platform, which is a turnkey solution that enables laboratories to conduct their own advanced cancer genomic testing using next-generation sequencing.

PGDx co-founder and Chief Medical Officer Luis Diaz, MD, noted, "As pioneers in the field of cancer genomics, we are delighted to be collaborating with HLI, a visionary company co-founded by genomics legend J. Craig Venter." PGDx co-founder and Chief Scientific Officer Victor Velculescu, MD, PhD, added, "HLI's commitment to changing the way medicine is practiced by systematically harnessing genomics data to address aging-associated diseases aligns well with our goal of transforming the treatment of cancer by enabling researchers, physicians and patients to use genomics data to advance and personalize cancer therapy."

PGDx applies its advanced genomic methods to identify and characterize the unique genomic alterations in tumors using tissue and liquid biopsies from cancer patients. The ES platform utilizes PGDx's proprietary bioinformatics software pipeline that provides industry-leading sensitivity and specificity, while maximizing accuracy in detecting multiple types of tumor-specific mutations. PGDx's targeted gene panels focus on well-characterized genes that have been selected for their high biologic importance in cancer and their relevance to drug targets and pathways.

HLI is building the world's largest and most comprehensive database of human genomic and phenotype data. The company has signed agreements with academic medical centers and large biotechnology companies to sequence and analyze human genomes, including those of cancer patients, to determine more precise treatments and more details about the specific tumor and cancer in that patient. The PGDx suite of solutions will enable even greater precision and detail for HLI's customers and their patients.

As part of the agreement, HLI will perform sequencing and analysis for select PGDx customers and for their own research activities.

"Having access to PGDx's capabilities, targeted cancer panels and Enterprise Solution platform for advanced cancer genomic testing is another important component to our already comprehensive and accurate database of human biological data," said J. Craig Venter, PhD, HLI's Co-founder, Chairman, and Chief Executive Officer. "We are excited to be partnering with PGDx and the extensive cancer genomics expertise and technology innovations developed by the world-class research team at PGDx."

About Personal Genome DiagnosticsPersonal Genome Diagnostics (PGDx) provides advanced cancer genome analyses to oncologyresearchers, drug developers, clinicians and patients. The company uses advanced genomic methods and its deep expertise in cancer biology to identify and characterize the unique genomic alterations in tumors. PGDx's proprietary methods for genome sequencing and analysis are complemented by its extensive experience in cancer genomics and clinical oncology. Co-founders Luis Diaz, MD, and Victor Velculescu, MD, PhD, are internationally recognized leaders in cancer genomics who have extensive experience in the practical application of advanced genomic technologies to research, drug development and clinical practice. PGDx's CLIA-certified facility provides personalized cancer genome analyses to patients and their physicians. For more information, visit http://www.personalgenome.com.

About Human Longevity, Inc.HLI, a privately held company headquartered in San Diego, CA was founded in 2013 by pioneers in the fields of genomics and stem cell therapy. Using advances in genomic sequencing, the human microbiome, proteomics, informatics, computing, and cell therapy technologies, HLI is building the world's most comprehensive database of human genotypes and phenotypes as a basis for a variety of commercialization opportunities to help solve aging related disease and human biological decline. HLI will be licensing access to its database, and developing new diagnostics and therapeutics as part of their product offerings. For more information please visitwww.humanlongevity.com

Contacts

PGDx Corporate: Antony Newton Chief Commercial Officer 443-602-8833 anewton@personalgenome.com

More:
Personal Genome Diagnostics, Inc. And Human Longevity, Inc ...

Posted in Human Longevity | Comments Off on Personal Genome Diagnostics, Inc. And Human Longevity, Inc …

Personal Genome Diagnostics, Inc. And Human Longevity, Inc. Sign Cancer Genomics Agreement

Posted: at 8:47 pm

BALTIMORE and LA JOLLA, Calif., Jan. 12, 2015 /PRNewswire/ --Personal Genome Diagnostics, Inc. (PGDx), a provider of advanced cancer genome analysis and testing services, and Human Longevity, Inc. (HLI), the human health information technology and health care company, today announced that HLI will have access to PGDx's cancer genomics solutions to expand its analysis of cancer genomes, including CancerSelect, PlasmaSelect, CancerXome, METDetect and CancerComplete. HLI has also licensed the PGDx Enterprise Solution platform, which is a turnkey solution that enables laboratories to conduct their own advanced cancer genomic testing using next-generation sequencing.

PGDx co-founder and Chief Medical Officer Luis Diaz, MD, noted, "As pioneers in the field of cancer genomics, we are delighted to be collaborating with HLI, a visionary company co-founded by genomics legend J. Craig Venter." PGDx co-founder and Chief Scientific Officer Victor Velculescu, MD, PhD, added, "HLI's commitment to changing the way medicine is practiced by systematically harnessing genomics data to address aging-associated diseases aligns well with our goal of transforming the treatment of cancer by enabling researchers, physicians and patients to use genomics data to advance and personalize cancer therapy."

PGDx applies its advanced genomic methods to identify and characterize the unique genomic alterations in tumors using tissue and liquid biopsies from cancer patients. The ES platform utilizes PGDx's proprietary bioinformatics software pipeline that provides industry-leading sensitivity and specificity, while maximizing accuracy in detecting multiple types of tumor-specific mutations. PGDx's targeted gene panels focus on well-characterized genes that have been selected for their high biologic importance in cancer and their relevance to drug targets and pathways.

HLI is building the world's largest and most comprehensive database of human genomic and phenotype data. The company has signed agreements with academic medical centers and large biotechnology companies to sequence and analyze human genomes, including those of cancer patients, to determine more precise treatments and more details about the specific tumor and cancer in that patient. The PGDx suite of solutions will enable even greater precision and detail for HLI's customers and their patients.

As part of the agreement, HLI will perform sequencing and analysis for select PGDx customers and for their own research activities.

"Having access to PGDx's capabilities, targeted cancer panels and Enterprise Solution platform for advanced cancer genomic testing is another important component to our already comprehensive and accurate database of human biological data," said J. Craig Venter, PhD, HLI's Co-founder, Chairman, and Chief Executive Officer. "We are excited to be partnering with PGDx and the extensive cancer genomics expertise and technology innovations developed by the world-class research team at PGDx."

About Personal Genome DiagnosticsPersonal Genome Diagnostics (PGDx) provides advanced cancer genome analyses to oncologyresearchers, drug developers, clinicians and patients. The company uses advanced genomic methods and its deep expertise in cancer biology to identify and characterize the unique genomic alterations in tumors. PGDx's proprietary methods for genome sequencing and analysis are complemented by its extensive experience in cancer genomics and clinical oncology. Co-founders Luis Diaz, MD, and Victor Velculescu, MD, PhD, are internationally recognized leaders in cancer genomics who have extensive experience in the practical application of advanced genomic technologies to research, drug development and clinical practice. PGDx's CLIA-certified facility provides personalized cancer genome analyses to patients and their physicians. For more information, visit http://www.personalgenome.com.

About Human Longevity, Inc.HLI, a privately held company headquartered in San Diego, CA was founded in 2013 by pioneers in the fields of genomics and stem cell therapy. Using advances in genomic sequencing, the human microbiome, proteomics, informatics, computing, and cell therapy technologies, HLI is building the world's most comprehensive database of human genotypes and phenotypes as a basis for a variety of commercialization opportunities to help solve aging related disease and human biological decline. HLI will be licensing access to its database, and developing new diagnostics and therapeutics as part of their product offerings. For more information please visitwww.humanlongevity.com

Contacts

PGDx Corporate: Antony Newton Chief Commercial Officer 443-602-8833 anewton@personalgenome.com

See the original post:
Personal Genome Diagnostics, Inc. And Human Longevity, Inc. Sign Cancer Genomics Agreement

Posted in Human Longevity | Comments Off on Personal Genome Diagnostics, Inc. And Human Longevity, Inc. Sign Cancer Genomics Agreement

Page 2,711«..1020..2,7102,7112,7122,713..2,7202,730..»