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Monthly Archives: March 2014
When Did Chickens Cross The Pacific Ocean? DNA Shows No Evidence Of Pre-Columbian Contact
Posted: March 18, 2014 at 9:44 pm
Ancient chicken DNA may shed light on the migratory patterns of early Polynesian people.
According to a new study published in the Proceedings of the National Academy of Sciences, ancient Polynesian chickens might not have migrated to South America as some scientists believe. Researchers came to their conclusion after comparing mitochondrial DNA taken from chicken bones from archeological sites in several Pacific islands with DNA taken from 122 feathers from modern chickens in the South Pacific.
"We were able to re-examine bones used in previous studies that had linked ancient Pacific and South American chickens, suggesting early human contact, and found that some of the results were contaminated with modern chicken DNA, which occurs at trace levels in many laboratory components," Professor Alan Cooper a professor from the University of Adelaide's Australian Centre for Ancient DNA said in a statement. "We were able to show that the ancient chicken DNA provided no evidence of any pre-Columbian contact between these areas."
The results showed that the chicken DNA had a distinct genetic marker that is not found in modern South American chickens, which suggests that the Polynesian and South American people did not have much contact.
"Indeed, the lack of the Polynesian sequences [of DNA] in modern South American chickens ... would argue against any trading contact as far as chickens go," Cooper told National Geographic.
By sequencing the ancient DNA, researchers were able to track the early movements and trading patterns in the Pacific.
"We can show [from chicken DNA] that the trail heads back into the Philippines," Cooper said. "We're currently working on tracing it farther northward from there. However, we're following a proxy, rather than the actual humans themselves."
The history behind the settlement of the Pacific Islands remains largely a mystery. Historians have determined the colonizing of the region took place in two phases: the first was more than 3,000 years ago when seafarers from Papua New Guinea sailed to islands like Vanuatu, Fiji, Tonga, Samoa, New Caledonia and populated them. The second took place around 800 A.D. when settlers came to the islands such as Tahiti, Bora Bora, the Marquesas, Easter Island, and Hawaii. To this day, exactly why and how these voyages were accomplished has left more questions than answers. Very few artifacts or writings remain.
"There are still many theories about where the early human colonists of the remote Pacific came from, which routes they followed and whether they made contact with the South American mainland, Jeremy Austin, ACAD Deputy Director said in a statement. Domestic animals, such as chickens, carried on these early voyages have left behind a genetic record that can solve some of these long standing mysteries."
One lingering question is whether the Polynesian people made it all the way to South America, and if they beat Christopher Columbus to it. The latest study says suggests this did not happen, but many scientists disagree.
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When Did Chickens Cross The Pacific Ocean? DNA Shows No Evidence Of Pre-Columbian Contact
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TeselaGen provides a rapid prototyping platform for DNA synthesis
Posted: at 9:44 pm
Following recent progress in DNA sequencing, California-based TeselaGen has developed a prototyping platform to help streamline synthetic biology experiments.
As the costs of DNA sequencing and synthesis plummet, a host of computer science-meets-biotech startups are emerging in Silicon Valley. Among the new players is San Francisco- headquartered TeselaGen, which creates middleware third party software which enables different IT applications to talk to each other for biotech labs looking to speed up the design and iteration of new DNA constructs. The company builds tools that help researchers set up and manage synthetic biology experiments and interpret data from lab equipment. According to TeselaGen CEO Mike Fero, the companys vision in developing a platform for rapid prototyping in synthetic biology is to help laboratories doing analysis to close the design-build-test-and-evolve loop. The company is currently backed by about $1 million in Small Business Innovation Research grants from theNational Science Foundation, an independent US government agency whose mission is to promote science and engineering through research programs and education projects.
The IT platform developed by TeselaGen aims to shorten the time frame it takes to get your DNA built and run more experiments, explains Mike Fero. TeselaGen has built visual tools that help researchers view, edit and manage sequences quickly and easily. The team has also created a design canvas that supports Synthetic Biology Open Language, an open set of standards that help synthetic biologists and genetic engineers share DNA designs. In addition they are leveraging j5, which is a new software-based tool that automates DNA assembly and design, promoting a faster design-build-test-and-evolve process. Like other companies in the field, TeselaGen gives its product away free to academic researchers, but charges corporate clients annual subscription fees.
A biologist might want to test 10,000 different variants of a design, with minor alterations in each. Right now, the cost of synthesizing each and every one of those constructs would be too expensive, and Mike Fero is hoping that that some of the products TeselaGen is building could in the future help to bring the costs of such experiments down considerably. Meanwhile, the advent of automated procedures in the biotechnology domain is reflected in the growth of companies such as scientific outsourcing provider Transcriptic, which runs fully automated labs, and Genome CompilerCorporation, which builds (CAM/CAD) design and manufacturing tools for biologists. Genome Compiler provides similar solutions to the sequence visualization tools that TeselaGen offers researchers, the major differences being that they are not based on Synthetic Biology Open Language and that Genome Complier does not use any equivalent to the j5 protocol. In the same way that large data flows are changing the way we solve problems nowadays, the next generation of synthetic biologists could well be relying solely on programming interfaces to carry out their experiments.
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TeselaGen provides a rapid prototyping platform for DNA synthesis
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There Is No Evidence For Evolution The Genome part 4 by Jason Burns – Video
Posted: at 9:43 pm
There Is No Evidence For Evolution The Genome part 4 by Jason Burns
Jason Burns can be found on the links below https://www.youtube.com/user/Zwemer100/featured https://www.youtube.com/user/TheBurnsShow/featured.
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There Is No Evidence For Evolution The Genome part 4 by Jason Burns - Video
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Scientists track evolution of a superbug
Posted: at 9:43 pm
Date:
March 17, 2014
Source:
NIH/National Institute of Allergy and Infectious Diseases
Summary:
Using genome sequencing, scientists have tracked the evolution of the antibiotic-resistant bacterium Klebsiella pneumoniae sequence type 258 (ST258), an important agent of hospital-acquired infections. While researchers had previously thought that ST258 K. pneumoniae strains spread from a single ancestor, the team showed that the strains arose from at least two different lineages.
Using genome sequencing, National Institutes of Health (NIH) scientists and their colleagues have tracked the evolution of the antibiotic-resistant bacterium Klebsiella pneumoniae sequence type 258 (ST258), an important agent of hospital-acquired infections. While researchers had previously thought that ST258 K. pneumoniae strains spread from a single ancestor, the NIH team showed that the strains arose from at least two different lineages. The investigators also found that the key difference between the two groups lies in the genes involved in production of the bacterium's outer coat, the primary region that interacts with the human immune system. Their results, which appear online in Proceedings of the National Academy of Sciences, promise to help guide the development of new strategies to diagnose, prevent and treat this emerging public health threat.
ST258 K. pneumoniae is the predominant cause of human infections among bacteria classified as carbapenem-resistant Enterobacteriaceae (CRE), which kill approximately 600 people annually in the United States and sicken thousands more. Most CRE infections occur in hospitals and long-term care facilities among patients who are already weakened by unrelated disease or have undergone certain medical procedures. In the new study, scientists from the NIH's National Institute of Allergy and Infectious Diseases (NIAID) and their colleagues sequenced the complete genomes of ST258 K. pneumoniae strains collected from two patients in New Jersey hospitals. By comparing these reference genomes with gene sequences from an additional 83 clinical ST258 K. pneumoniae isolates, the scientists found that the strains divided broadly into two distinct groups, each with its own evolutionary history. Further analysis revealed that most differences between the two groups occur in a single "hotspot" of the genome containing genes that produce parts of the bacterium's outer shell. The investigators plan to further study how these genetic differences may affect the bacterium's ability to evade the human immune system.
The findings from this study highlight the wealth of information that can be gained from genome sequencing. They also demonstrate the importance of sequencing to the surveillance and accurate tracking of bacterial spread. Study collaborators included NIAID-funded scientists from Public Health Research Institute and New Jersey Medical School-Rutgers University, as well as researchers from Case Western Reserve University, the Houston Methodist Research Institute and Hospital System and NIAID's Rocky Mountain Laboratories, where the comparative genome sequencing took place.
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From DNA to Diagnosis: USTAR Center for Genetic Discovery to Integrate Genome Data into Patient Care
Posted: at 9:43 pm
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Newswise SALT LAKE CITY The USTAR Center for Genetic Discovery is partnering with California based Omicia, Inc, to make analyzing a patients genome as routine as performing a blood test. The center, co-directed by Mark Yandell, Ph.D., and Gabor Marth, D.Sc., was launched this month with $6 million from the University of Utah and the state-funded Utah Science Technology and Research (USTAR) initiative.
Compared to 10 years ago, sequencing the human genome has plummeted in cost by 1 million-fold and can be completed in a fraction of the time. Yet there are still barriers preventing DNA sequence information from routinely being incorporated into patient care.
Current systems are not prepared for the increasing amounts of data we will be seeing within the next few years, said Marth, a computer scientist who was instrumental in the success of high profile projects such as the Human Genome Project, HapMap Project, and 1,000 Genomes Project. He relocated to the University of Utah from Boston College to apply his skills in a medical setting.
At some point all of humanity will be sequenced, and potentially more than one genome per individual, he continued. Marth and Yandell will lead efforts to tame the big data to come not only from personal genomes, but also tumor genomes and metagenomes from infectious disease agents such as viruses and bacteria.
Knowing the DNA sequence of a cancer patients tumor, for example, may reveal a personalized treatment plan for combatting the disease. Pinpointing tiny sequence variations in personal genomes will expose inherited diseases that, in some cases, may be life-threatening.
What we want to be able to do is help the kid who is born with a hard-to-diagnose genetic disorder, said Yandell. Our genome interpretation tools will be able to identify that disorder and guide treatment.
Together with Omicia, Inc., the USTAR Center for Genetic Discovery is building a web accessible informatics platform, called Opal, to distill genome data to clinically relevant findings. Opal is powered by VAAST, a proven disease gene finder algorithm invented by Yandell. Launched less than two years ago, VAAST has successfully identified causes of inherited diseases, including hard-to-diagnose rare diseases, and is used at 251 institutions worldwide.
The USTAR Center for Genetic Discovery eventually anticipates commercializing its full suite of software tools, and becoming a top genomic health data service provider for medical centers nationwide.
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From DNA to Diagnosis: USTAR Center for Genetic Discovery to Integrate Genome Data into Patient Care
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How To Get Rid Of Eczema Naturally – Video
Posted: at 9:43 pm
How To Get Rid Of Eczema Naturally
How To Get Rid Of Eczema - http://HowToGetRidOfEczemaNaturally.org - Looking for information on how to get rid of eczema naturally, and for good? This video ...
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How To Get Rid Of Eczema Naturally - Video
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NEOSPORIN ECZEMA ESSENTIALS Product Demo Video – Video
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NEOSPORIN ECZEMA ESSENTIALS Product Demo Video
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Eczema Creams that I Use – Video
Posted: at 9:43 pm
Eczema Creams that I Use
Here are the Eczema creams that I use for my Eczema and dry skin. I try to stick to using fragrance free creams and soaps (or soaps with a mild fragrance) as...
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Eczema Creams that I Use - Video
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Psoriasis, causes, treatment, management – Video
Posted: at 9:43 pm
Psoriasis, causes, treatment, management
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Psoriasis, causes, treatment, management - Video
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New gene linked to key heart attack risk factor found by novel gene-finding approach
Posted: at 9:43 pm
Scientists have discovered a previously unrecognized gene variation that makes humans have healthier blood lipid levels and reduced risk of heart attacks -- a finding that opens the door to using this knowledge in testing or treatment of high cholesterol and other lipid disorders.
But even more significant is how they found the gene, which had been hiding in plain sight in previous hunts for genes that influence cardiovascular risk.
This region of DNA where it was found had been implicated as being important in controlling blood lipid levels in a report from several members of the same research team in 2008. But although this DNA region had many genes, none of them had any obvious link to blood lipid levels. The promise of an entirely new lipid-related gene took another six years and a new approach to find.
In a new paper in Nature Genetics, a team from the University of Michigan and the Norwegian University of Science and Technology report that they zeroed in on the gene in an entirely new way.
The team scanned the genetic information available from a biobank of thousands of Norwegians, focusing on variations in genes that change the way proteins function. Most of what they found turned out to be already known to affect cholesterol levels and other blood lipids.
But one gene, dubbed TM6SF2, wasn't on the radar at all. In a minority of the Norwegians who carried a particular change in the gene, blood lipid levels were much healthier and they had a lower rate of heart attack. And when the researchers boosted or suppressed the gene in mice, they saw the same effect on the animals' blood lipid levels.
"Cardiovascular disease presents such a huge impact on people's lives that we should leave no stone unturned in the search for the genes that cause heart attack," says Cristen Willer, Ph.D., the senior author of the paper and an assistant professor of Internal Medicine, Human Genetics and Computational Medicine & Bioinformatics at the U-M Medical School.
"While genetic studies that focused on common variations may explain as much as 30 percent of the genetic component of lipid disorders, we still don't know where the rest of the genetic risk comes from," Willer adds. "This approach of focusing on protein-changing variation may help us zero in on new genes faster."
Willer and Kristian Hveem of the Norwegian University of Science and Technology led the team that published the new result. Intriguingly, Willer and colleagues suggest the same gene may also be involved in regulating lipid levels in the liver -- a finding confirmed by the observations of a team led by Jonathan Cohen and Helen Hobbs, who propose a role for the gene in liver disease in the same issue of Nature Genetics.
Hveem, a gastroenterologist, says that "more research into the exact function of this protein will be needed to understand the role it plays in these two diseases, and whether it can be targeted with new drug therapies to reduce risk -- or treat -- one or both diseases."
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New gene linked to key heart attack risk factor found by novel gene-finding approach
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