Who's Your Daddy? Mobile Truck Offers DNA Tests to Go

Aug 16, 2012 4:06pm

Image credit: WABC

In what may be a first anywhere, a Whos Your Daddy truck is cruising New York City selling DNA tests to people who want to confirm their childs paternity or even whether their parents are biologically related to them.

The brown and white RV, which is bedecked in eye catching signs advertising its services, is more than just a moving billboard, according to driver and operator Jared Rosenthal. The RV is set up to be a drug testing clinic and a DNA testing clinic, he told ABC News. Its essentially a mobile office so while were working people will walk up and ask questions and sometimes even take a test right on board.

Rosenthal, who works at mobile and clinic based testing company Health Street, came up with the idea for the truck himself.Necessity is the mother of invention, he said. Icouldntafford to rent an office, so I thought, we can convert the RV to a mobile office. People love the artworkit makes them smile and they share it with their friends on social media and get in touch with people who maybe do need DNA tests.

But its not all smiles aboard the Whos Your Daddy Truck, which often plays host to the full spectrum of human emotions. DNA really gets at a persons identity, it gets to the core of their identity, who your parents are, who your children are, how you define yourself ethnically and culturally. Rosenthal said The RV is a little more intimate than a clinic,clients tend to talk more they tell us things, we experience some of these life-changing moments with them.

Rosenthal brought up the story of one woman in her early 20s who came in for a test, only to find out that the people she believed to be her father and her three half-sisters was not related to her at all. In fact, the test revealed she was from an entirely different ethnic background. When she found out her father wasnt her biological father it totally rocked her identity to the core, he said.

He recounted meeting an 18-year-old woman from another state who had contacted the man she believed to be her father living in New York. A DNA test at the truck proved it was true, bringing a broken family back together. He began to form a relationship with this woman and it was great. Rosenthal said. They lost 18 years but they found each other.

Drama aside, Rosenthal insists that the truck is much more than a mobile Maury, providing a service that is very approachable, very accessible, and very available to the community.

The DNA, drug, and alcohol tests, which range in price from $79 to$599 are available at the truck or at local health street clinics. Although based in New York, the organization has partnered with out-of-state clinics and the US Consulate to provide testing in the event that one or more of the parties may live out of the state or country.

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Who's Your Daddy? Mobile Truck Offers DNA Tests to Go

Posted in DNA

DNA Data Storage

Researchers code a book into DNA, demonstrating the possibility of using the biological molecule for long-term data storage.

Coding messages into DNA was first demonstrated in the 1980s, but technology at the time would only allow one graphical symbol to be encoded. While that capacity has grown over the last 3 decades, the largest project to date, completed in 2010, managed just 7,920 bits of data, equating to approximately half a page of typed text. Using a novel technique, detailed today in Science, researchers at Harvard and Johns Hopkins Universities, have now encoded a 53,000-word book into DNA, including 11 JPG images and one JavaScript program.

Others have pointed out that DNA has certain advantages, said study co-author Sriram Kosuri. But no one had really taken it to a level that we were able to code really useful amounts of information.

Those advantages include the density of information that can be stored: an estimate of maximum capacity predicts that one gram of single-strand DNA could store as much as an exabyte (1018 bytes) of data. However, synthesizing and sequencing DNA carries a lot of inherent errors. Synthetic DNA typically has one incorrect nucleotide in every 70, and next gen sequencing techniques can make many mistakes when interpreting the stored data.

To overcome such errors, the team assigned the bases A and C as 0s, and G and T as 1s, creating a digital data stream. The manuscript and its accompanimentsa draft version of a book co-authored by one of the studys authors, George Church, called Regenesis: How Synthetic Biology Will Reinvent Nature and Ourselveswas converted to HTML before being translated into the stream of 0s and 1s that could be written into the DNA sequence. The resulting stream was 5.27 megabits long, or 5.27 million 0s and 1s.

Previous methods have faced problems when trying to create whole streams in one long DNA sequence, a tricky and expensive process. The teams solution was to split the stream into smaller sections. They coded 96 bits per short nucleotide section, called an oligonucleotide, each of which contained a 19-bit address to order the information in the overall sequence. Each oligonucleotide was synthesized multiple times, so that upon reading, errors could be compared in each copy and a consensus reading could be reached.

Its a similar in the way that when you sequence the human genome, you dont sequence it once, you sequence it at 30 or 50 times coverage, and you just take consensus at each position, said Kosuri.

After synthesizing the sequence and attaching drops of DNA to microarray chips, the data was stored at 4 degrees Celsius for 3 months before being dissolved in water, amplified by PCR, and sequenced. By storing multiple copies, and sequencing each copy many times to reach consensus, the team managed to decode the entire 5.27-million-bit sequence with only 10 bit errors.

Theyve come up with a very clever way of managing error in the creation of the information, said synthetic biologist Steven Benner at the Foundation for Applied Molecular Evolution, who was not involved in the study. [The authors] provide some clever ways to get around the problems, allowing the reading of the minority molecules containing the desired information amid the larger numbers of molecules that do not.

While DNA storage is not re-writable, and not intended to replace your hard drive, the idea of long-term storage of large amounts of data in a very small space has advantages for archiving records and data. In contrast to a flat disc like a CD, with data only inscribed on the surface, a sheet of DNA has data stored throughout its thickness. The major challenge that remains, however, is the cost and efficiency of todays synthesizing and sequencing technologies, which currently make this system impractical for regular use. As sequencing costs continue to drop and technologies continue to advance, however, such DNA storage strategies may soon become much more practical.

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DNA Data Storage

Posted in DNA

Reading and Writing a Book With DNA

16 August 2012Harvard University researchers converted a 53 000-word book into DNA and then read the DNA-encoded book using gene-sequencing technology, the researchers report this week in Science. The project is by far the largest demonstration of digital information storage in DNA and the densest consolidation of data in any medium, the authors say.

There is a clear need for improved long-term storage of massively large data, says George Church, a geneticist at Harvards Wyss Institute and one of the leaders of the research. There is data that we are throwing away or dont collect because we cant afford to store it, such as video surveillance of public spaces and large research projects, he says. Someday that wont be necessary. The question is, What will get us there first: electronic or molecular memory?

DNA offers advantages over electronic storage, but whether it will ever make sense practically or economically is unclear. DNA can store more digital information per cubic millimeter than flash memory or even cutting-edge experimental memories such as quantum holography. Data stored in DNA is also recoverable for millennia (consider the 7000-year-old DNA archaeologists have extracted from human remains). And given DNAs biological importance, we can safely assume its going to remain a readable standard for a long time. If you look at the size per bit of stored memory as DNA, its unlikely that well ever get better than that, says Joseph Jacobson, a synthetic biologist at MIT who was not involved in the project.

But making and reading DNA isnt yet practical. Synthesizing and sequencing DNA is expensive, although the cost for both of these technologies has been dropping at a rate of five- and twelvefold per year, respectively. Whats more, unlike electronic bits, most DNA data cannot be changed once its written. And with todays technology, information in DNA usually has to be accessed as a whole, not in parts. (There is no way to make random-access DNA memory.)

Church and his colleagues set out to demonstrate a simple way to densely store data in DNA. They converted an html draft of a book comprising 53 426 words, 11 JPG images, and one JavaScript program into a 5.27 megabit set of zeros and ones. Using software they wrote, zeros were assigned the letter A or C for the DNA bases adenine and cytosine, and ones were assigned the letter G or T for DNA bases guanine and thymine. A lowercase f from the book, for example, was represented in binary as 01100110 and encoded in DNA as ATGAATTC.

Synthesizing that string of bits would yield a stretch of DNA that was 5.27 million bases long. Such long stretches of DNA are particularly expensive to work with, so Church and his colleagues split the DNA sequence into short chunks that were each 96 bases long. Each chunk included a 19-bit bar code, or address, to show where that chunk belonged in the whole of the book. The DNA was synthesized, inkjet-printed on a glass DNA microchip, and then cleaved off and dried to form a 50-nanogram clump smaller than a speck of pollen.

To convert the DNA back to a book, Church and his colleagues read out the bases using commercially available sequencing technology. They then arranged the sequence, decoded it back to zeros and ones, and converted those back to an HTML book. The researchers were able to complete the project with errors in only 10 bits out of 5.27 millionon par with the raw error rate of other storage media, says Sriram Kosuri, a staff scientist at the Wyss Institute who also worked on the project.

The tome that got the honor of becoming the worlds first biological book is the forthcoming Regenesis: How Synthetic Biology Will Reinvent Nature and Ourselves. The book, coauthored by Church, will be published in more conventional forms this fall.

Similar approaches have been demonstrated before, but on a smaller scale. In 2001, Carter Bancroft and his colleagues at the Mount Sinai School of Medicine encoded in DNA the opening lines of Charles Dickenss A Tale of Two Cities. A 2010 project from the J. Craig Venter Institute encoded a 7920-bit watermark in a bacterium genome sequence. Churchs paper, however, takes us from a few bits to many megabits, says Jacobson. If you have a big enough quantitative advance, at some point theres a qualitative shift, and Id say thats the case here.

But another researcher who studies the intersection of biology and technology and asked to remain anonymous calls Churchs paper a silly vanity project with little value. Its like showing you could painstakingly use an abacus to solve a Hamiltonian path problem that would take the average computer a microsecond, he says. Other than maybe military intelligence, finding real-world applications for DNA storage technology under no conceivable set of circumstances is even remotely likely, he says.

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Reading and Writing a Book With DNA

Posted in DNA

An Entire Book Written in DNA

DNA can be used to store information at a density about a million times greater than your hard drive, report researchers in Science today. George Church of Harvard Medical School and colleagues report that they have written an entire book in DNA, a feat that highlights the recent advances in DNA synthesis and sequencing.

The team encoded a draft HTML version of a book co-written by Church called Regenesis: How Synthetic Biology Will Reinvent Nature and Ourselves. In addition to the text, the biological bits included the information for modern formatting, images and Javascript, to show that DNA (like other digital media) can encode executable directives for digital machines, they write.

To do this, the authors converted the computational language of 0's and 1's into the language of DNA--the nucleotides typically represented by A's, T's G's and C's; the As and Cs took the place of 0's and Ts and Gs of 1's. They then used off-the-shelf DNA synthesizers to make 54,898 pieces of DNA, each 159 nucleotides long, to encode the book, which could then be decoded with DNA sequencing.

This is not the first time non-biological information has been stored in DNA, but Church's demonstration goes far beyond the amount of information stored in previous efforts. For example, in 2009, researchers encoded 1688 bits of text, music and imagery in DNA and in 2010, Craig Venter and colleagues encoded a watermarked, synthetic genome worth 7920 bits.

DNA synthesis and sequencing is still too slow and costly to be practical for most data storage, but the authors suggest DNAs long-lived nature could make it a suitable medium for archival storage.

Erik Winfree, who studies DNA-based computation at Caltech and was a 1999 TR35 winner, hopes the study will stimulate a serious discussion about what roles DNA can play in information science and technology.

The most remarkable thing about DNA is its information density, which is roughly one bit per cubic nanometer, he writes in an email.

Technology changes things, and many old ideas for DNA information storage and information processing deserve to be revisited now -- especially since DNA synthesis and sequencing technology will continue their remarkable advance.

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An Entire Book Written in DNA

Posted in DNA

Book converted to DNA then 'read' to show off bio-digital storage

6 hrs.

Francie Diep , InnovationNewsDaily

Bioengineers have turned a book into DNA. The researchers also have shown they can decode the DNA to re-create the book, which includes 53,426 words, 11 images and one interactive Javascript app.

This may be the world's only modern biology book that costs thousands of dollars to read as well as write.

The new bio-digital book, coded from a Harvard University researcher's writings on synthetic biology, represents the largest amount ofdata ever written into DNA. Because of how costly and complex it is to read and write genetic material, DNA is still far from a practical storage drive. Yet as the price of synthesizing and sequencing DNA continues to drop, it may become an interesting way of storing data for the very long term, said Sriram Kosuri, a Harvard bioengineer who was one of the bio-digital book's creators.

"It brings a different perspective into the storage field," Kosuri told InnovationNewsDaily.

"At this point, it's very premature to hope that it would actually become something practical," said Stefano Lonardi, a computational biologist at the University of California, Riverside, who was not part of the Harvard effort. Nevertheless, Lonardi said, the work is a step toward DNA storage in the future. "These are things that people have to do first in order to get to something practical," he said.

Turning an e-book into DNATo turn text and pictures into a double helix, the book had to undergo several translations. First, Kosuri and his colleagues wrote an HTML file of a draft of the book that Harvard bioengineer George Church was writing at the time. HTML is the language Web developers use to write websites.

The biologists then turned the HTML into binary, the 1s and 0s that computers read. They decided to use the individual building blocks of DNA, commonly referred to by their one-letter initials, to represent the 1s and 0s. The building blocks A and C would represent 0s, they decided, while G and T would represent 1s. They then assembled strands of DNA representing their binary code. [10 Technologies Poised to Transform our World]

One of the greatest challenges of building DNA from scratch is that it's expensive and difficult to create long, unbroken strings of the stuff. So Kosuri and his teammates decided they would make very many smaller pieces instead, tagging each piece with an address so that someone trying to read the strands would be able to put them in the correct order. Such pieces are easy for the latest DNA-reading technology, callednext-generation sequencing, to process.

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Book converted to DNA then 'read' to show off bio-digital storage

Posted in DNA

DNA Sample Concentrator uses centrifugal force and vacuum.

August 16, 2012 - With built-in, removable diaphragm pump, CentriVap DNA Centrifugal Concentrator processes DNA samples and other minute quantities of solvents. Up to 60, 1.5 mL and 72, 0.5 mL micro centrifuge tubes may be processed simultaneously. There are 9 user-set programs accessible via buttons, and Quick-Start(TM) One Button Start Up function starts rotor, heater, timers, and vacuum pump. Along with Quick-Stop(TM) Rotor Brake, features include inlet and exhaust traps and optional CentriZap Strobe Light. Original Press release Labconco Corp. 8811 Prospect Ave. Kansas City, MO, 64132 2696 USA The CentriVap DNA Centrifugal Concentrator processes DNA samples and other minute quantities of solvents. Up to 60 each 1.5 ml and 72 each 0.5 ml micro centrifuge tubes may be processed at once.

With a built-in, removable diaphragm pump, the CentriVap DNA Concentrator has 9 user-set programs accessible with the touch of a few buttons. The Quick-Start(TM) One Button Start Up starts the rotor, heater, timers and vacuum pump. Three Quick-Start Buttons store one user-set program each. The Quick-Stop(TM) Rotor Brake stops vacuum within seconds to open the valve and bleed air into the chamber. Separate heat and run times allow the heat to be turned off sooner than the rotation to protect heat sensitive samples from excessive heat exposure. The Run Time turns off all functions after the set period of time has expired. Both an inlet trap to collect liquid coming off the samples and an exhaust trap to collect liquid coming off the pump exhaust are included. An optional CentriZap Strobe Light which utilizes a flashing light the same frequency as the rotation of the rotor allows remaining samples to be viewed in either sample tube or microtiter plate while it is spinning.

For more information on the CentriVap DNA Concentrator and the rest of the CentriVap line, contact Labconco at 800-732-0031, or download the PDF brochure at http://www.labconco.com.

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DNA Sample Concentrator uses centrifugal force and vacuum.

Posted in DNA

DNA Dynamics Announce SLAM Engine Overhaul

LEAMINGTON SPA, England, Aug. 16, 2012 /PRNewswire/ --DNA Dynamics, Inc. (OTC Pink: DNAD), a global developer and publisher of mobile video games and applications, today announced that the latest iteration of it's SLAM Engine Technology, SLAM V7.0, is currently in development.

The SLAM Engine is DNA's powerful proprietary technology on which all of its internally developed games are built. SLAM 6.x has been in use over the last 18 months however the gaming world has moved on in that time. The SLAM Engine has always been focused on delivering games on multiple platforms over a short development cycle and SLAM 7.0 takes this ethos to the next level. Built around the popular programing language of C# and the Mono Framework SLAM 7.0 will see DNA's next batch of games move on from both technical and time to market standpoints

Ed Blincoe, CEO of DNA Dynamics Inc., commented, "Redeveloping the SLAM Engine has been a major undertaking for the team however it was critical we keep ahead of the pack in terms of our development processes and time to market. Our next game is currently being built upon the new technology base and we've already seen a marked improvement in game performance and build speed, I'm excited about what we can achieve using the new SLAM Engine and the games it will produce." Blincoe continued, "By utilizing our own technology we can substantially reduces our development costs making us a company to watch into 2013."

The DNA Studios Team is currently transitioning over to the new technology base and expects to have its first game to market before the end of the year.

About DNA Dynamics, Inc.Headquartered in Leamington Spa in the United Kingdom, DNA Dynamics is a worldwide developer and publisher of graphically rich, interactive entertainment currently delivered on iOS, Android, Apple Mac and PC. Through its operating subsidiaries, the Company has created, acquired or licensed a portfolio of highly recognizable or emerging brands that broadly appeal to its consumer demographics, ranging from children to adults and casual gamers to serious enthusiasts. For more information, please go to http://www.dnadynamics.net.You can also follow the Company on Facebook and Twitter.

For more information please email info@dna-interactive.com.

Forward-Looking StatementsThis press release may contain forward-looking statements, including information about management's view of DNA Dynamics, Inc.'s future expectations, plans and prospects. In particular, when used in the preceding discussion, the words "believes," "expects," "intends," "plans," "anticipates," or "may," and similar conditional expressions are intended to identify forward-looking statements. Any statements made in this news release other than those of historical fact, about an action, event or development, are forward-looking statements. These statements involve known and unknown risks, uncertainties and other factors, which may cause the results of DNA Dynamics, its subsidiaries and concepts to be materially different than those expressed or implied in such statements. Unknown or unpredictable factors also could have material adverse effects on DNA Dynamics' future results. The forward-looking statements included in this press release are made only as of the date hereof. DNA Dynamics cannot guarantee future results, levels of activity, performance or achievements. Accordingly, you should not place undue reliance on these forward-looking statements. Finally, DNA Dynamics undertakes no obligation to update these statements after the date of this release, except as required by law, and also takes no obligation to update or correct information prepared by third parties that are not paid for by DNA Dynamics.

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DNA Dynamics Announce SLAM Engine Overhaul

Posted in DNA

DNA evidence clears Louisville man of murder charges

by Gene Kang

WHAS11.com

Posted on August 15, 2012 at 12:37 PM

Updated today at 6:41 PM

LOUISVILLE, Ky (WHAS11) -- A Louisville man who faced the death penalty is free tonight. Thats after prosecutors dropped a murder charge against him. It was DNA evidence that ultimately cleared him but not before he spent several years behind bars.

The Hall of Justice is where Carlos Lagantta claimed his freedom in more ways than one. He was waiting for trial for five years three for the current case and two for an unrelated charge. But Lagantta says he never grew bitter after being wrongfully accused of murder.

Overall, Carlos Lagantta served three years in prison for a murder he did not commit. He felt an overwhelming sense of freedom as a court of law declared that he's innocent.

WHAS 11 News: "What are you doing here at the Hall of Justice today?" "I'm turning in my HIP equipment and being a free man. Once I turn this in I'm all the way free," said Lagantta.

"Not only did he put this behind him but he was facing the death penalty," said Ryan Vantrease, Laganttas lawyer.

"It is the Commonwealth's decision to dismiss without prejudice," said prosecution in Judge Audra Eckerles court in Jefferson County.

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DNA evidence clears Louisville man of murder charges

Posted in DNA

PLoS ONE launches Synthetic Biology Collection

Public release date: 15-Aug-2012 [ | E-mail | Share ]

Contact: Yael Franco yfranco@plos.org 415-568-3169 Public Library of Science

PLoS ONE announces the launch of the Synthetic Biology Collection. The new Collection contains an unprecedented number of articles illustrating the many facets of this dynamically evolving research area.

The field of synthetic biology interconnects many engineering and scientific disciplines including biology, chemical engineering, chemistry, electrical engineering, and computer science. PLoS ONE has published more than 50 articles covering all aspects of synthetic biology. The journal aims to help increase the visibility of this growing transdisciplinary field by assembling the articles into a Collection.

"When working at its best, science should be an active conversation that keeps refining ideas," said Damian Pattinson, PLoS ONE's Executive Editor, "We believe that PLoS ONE provides the ideal venue to achieve this and we hope that the Collection will inspire further progress in synthetic biology."

PLoS ONE's innovative editorial policy has made it possible for synthetic biologists to publish research that may not be the proper fit for a classical journal.

"The collection includes several articles from engineers and computer scientists who traditionally publish their work in conference proceedings rather than the journals available to life-scientists," said Dr. Jean Peccoud, an Associate Professor at Virginia Bioinformatics Institute. "PLoS ONE's breadth of subject matter made it possible to publish an unprecedented body of articles that reflects the multifaceted nature of synthetic biology."

A key feature of PLoS ONE is the inclusion of article-level metrics (ALMs) that are published alongside each paper and can be used to assess the impact of the research.

"Two articles now included in the Collection, were published in 2006, and to date have been cited 70 and 84 times, respectively," said Dr. Mark Isalan, Group Leader at the Centre for Genomic Regulation. "Metrics such as social bookmarking or number of views lead us to believe that articles published more recently will also have a lasting impact on the field."

The Collection highlights selected synthetic biology articles published in PLoS ONE since 2006. It will be updated regularly with appropriate new papers, as a growing resource. "Ultimately, we hope that having a dedicated repository in PLoS ONE will further increase the journal's attractiveness to researchers publishing synthetic biology," said Pattinson.

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PLoS ONE launches Synthetic Biology Collection

Redskins’ Alexander shrinks to play linebacker

ASHBURN, Va. (AP) -- Lorenzo Alexander has quite a collection of white bottles, labeled with words straight from a biochemistry class. Beta Alanine Supreme. Carnitine Synergy. Uber C. Some 19 containers, big and small, in his Washington Redskins locker.

''I have a lot of supplements,'' he said.

The consummate self-made NFL player, Alexander has always been conscious about his diet. Like many players, he also gets advice on the right mix of tablets to maximize his endurance and energy output. Or, as he puts it, ''to help balance your body out.''

This year, it's been more of a challenge to find that balance. Alexander, who once was a 300-pound lineman, arrived at training camp weighing 245, having dropped some 30 pounds from this time last season so that he can hold his own in his new role as the team's primary backup at inside linebacker.

''Being 265,'' he said, ''is not ideal for covering tight ends and fast wide receivers down the middle of the field.''

No one would expect anything different from the player who arrived as a practice squad nobody in 2006 and soon became an indispensable utility man, working his way up to his current role as a team captain who now gets annual support from his teammates as an ought-to-be Pro Bowl player.

''I'd say he's one of, if not the biggest influence I've had since I've been here,'' said linebacker Ryan Kerrigan, a first-round draft pick last year. ''He seems to me what really embodies a professional. Not just a professional athlete, but a professional human being. He shows you what hard work can do.''

Alexander was a novelty his rookie season, a three-way player who saw game action on the offensive line, defensive line and special teams. He made his name with hard work, smarts and big special teams hits.

In 2010, the Redskins (No. 25 in the AP Pro32) moved him to outside linebacker. Last year, he started learning the inside linebacker position. This year, it's his main focus on the only experienced alternative to starters London Fletcher and Perry Riley in the 3-4 scheme.

Alexander's weight loss has been noticeable during training camp. He broke up a pass over the middle to Santana Moss during Wednesday's practice, the type of play he couldn't have made when he was a lot heavier.

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Redskins' Alexander shrinks to play linebacker

CSHL-led team introduces new method to closely model diseases caused by splicing defects

Public release date: 14-Aug-2012 [ | E-mail | Share ]

Contact: Peter Tarr tarr@cshl.edu 516-367-8455 Cold Spring Harbor Laboratory

Cold Spring Harbor, NY A team led by scientists at Cold Spring Harbor Laboratory (CSHL) has developed a new way of making animal models for a broad class of human genetic diseases those with pathology caused by errors in the splicing of RNA messages copied from genes. To date, about 6,000 such RNA "editing" errors have been found in various human illnesses, ranging from neurodegenerative disorders to cancer.

The new modeling approach can provide unique insights into how certain diseases progress and is likely to boost efforts to develop novel treatments. It was tested successfully by the CSHL team, led by Professor Adrian Krainer, Ph.D., in collaboration with scientists from Isis Pharmaceuticals, in mouse analogs of human spinal muscular atrophy (SMA), a motor-neuron disease that is the leading genetic cause of childhood mortality. The results are detailed in a study published today in Genes & Development.

The modeling method is called TSUNAMI (shorthand for targeting-splicing using negative ASOs to model illness). The study demonstrates it can be used in illnesses with pathology associated with the missplicing of pre-mRNAs unedited RNA molecules that bear the messages encoded in genes which provide instructions for cells to manufacture specific proteins.

Correcting splicing errors in SMA

A cellular machine called the spliceosome routinely snips non-essential bits called "introns" out of every pre-mRNA molecule that carries a copy of a gene's instructions. All that should remain after the spliceosome has done its work is a string of spliced-together "exons," the protein-encoding portions of the message. These edited mRNA messages are subsequently read by ribosomes, the cellular factories where proteins are synthesized.

In SMA and some other human illnesses, pathology can be traced to errors in the pre-mRNA editing process. In SMA, it is caused either by a severe mutation in a gene called SMN1 ("survival of motor neuron-1") or by that gene's complete absence in an affected individual's genetic material. The SMN protein normally encoded by the gene is essential for motor neuron development. Humans have a second, similar gene called SMN2, but it is a poor backup. Because of an error in the splicing of its pre-mRNA, the SMN2 gene, when expressed, typically produces only a fraction of the SMN protein needed by motor neurons. This is critical in the first stages of life when the body and muscles are still developing.

While the level of the "backup" gene's protein output varies in individuals with spinal muscular atrophy, resulting in pathology of varying intensity, Krainer -- a leading expert on splicing -- and his collaborators have succeeded in recent years in devising a method of getting SMN2 to produce therapeutic amounts of protein, enough to reverse pathology in both mild and severe mouse analogs of the disorder.

To achieve this they synthesized tiny snippets of RNA called ASOs (antisense oligonucleotides) and injected them into the cerebrospinal fluid of mice carrying a human SMN2 transgene (i.e., a gene not native to mice). This enabled them to get the therapeutic ASOs through the so-called blood-brain barrier, to reach cells throughout the central nervous system. ASOs are configured to attach at highly specific spots in pre-mRNAs, where, by design, they can inhibit activators or repressors of the splicing process. Krainer's team synthesized an ASO that corrected the SMN2 splicing error and gave rise to therapeutic amounts of SMN protein. Importantly, the ASO was shown to be stable in the body as well as persistent, the effects of a single injection lasting at least half a year in mice.

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CSHL-led team introduces new method to closely model diseases caused by splicing defects

Research and Markets: Sports Nutrition in Hong Kong, China

DUBLIN--(BUSINESS WIRE)--

Research and Markets (http://www.researchandmarkets.com/research/dd4skv/sports_nutrition_i) has announced the addition of the "Sports Nutrition in Hong Kong, China" report to their offering.

In Hong Kong sports nutrition products were mostly used by serious athletes in 2011, which is a niche market. Typical consumers were not aware of these products, nor was there a demand for them.

The Sports Nutrition in Hong Kong, China report offers a comprehensive guide to the size and shape of the market at a national level. It provides the latest retail sales data 2007-2011, allowing you to identify the sectors driving growth. Forecasts to 2016 illustrate how the market is set to change.

Product coverage: Non-Protein Products, Protein Products.

Data coverage: market sizes (historic and forecasts), company shares, brand shares and distribution data.

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Research and Markets: Sports Nutrition in Hong Kong, China

DNA evidence 'gobsmacked' accused

15 August 2012 Last updated at 09:38 ET

The man accused of murdering a Perthshire pensioner was "gobsmacked" to learn a partial profile of his DNA was found on her wrist, a court heard.

The jury was read parts of William Kean's police interviews which took place in March, the month after 80-year-old Jenny Methven was found dead.

Mr Kean, 46, denies killing Mrs Methven at her Forteviot home on 20 February.

He has lodged a special defence blaming the victim's son David Methven, or others connected to him.

The High Court in Glasgow heard Mr Kean told police during the interview that he did not assault Mrs Methven.

Det Sgt Brian Smith had told the accused he was offering him a chance to explain what had happened.

Mr Kean denied murdering Mrs Methven but replied "no comment" when asked if he had been in her house and then refused to explain that answer.

He also told officers that if he knew who was involved in her murder, he would tell them.

Mr Kean had said to officers: "I wish I did. I wish someone would come forward and admit it. It's a sad time for everybody."

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DNA evidence 'gobsmacked' accused

Posted in DNA

Scientists identify previously unknown Whimbrel migration pathway over open Atlantic Ocean

Fletcher Smith with Akpik on breeding grounds in the Canadian Arctic.

(Phys.org) -- Scientists at the College of William & Mary/Virginia Commonwealth University Center for Conservation Biology (CCB) at the VCU Rice Center have tracked three whimbrels off the east coast of Canada to the northern shore of South America via a previously unknown migration pathway over the open Atlantic Ocean. The route passed through the center of the vast Atlantic at one point passing 1,000 miles closer to Africa than to North America and within 700 miles of the Cape Verde Islands. The bird with the longest flight flew nonstop for 145 hours (six days), covering a distance of 7,000 kilometers (4,355 miles).

The three birds, named Mackenzie, Taglu and Akpik, were originally marked by the CCB and Canadian Wildlife Service staff on the breeding grounds along the Mackenzie River Delta in far northwestern Canada (Mackenzie was fitted with a transmitter recovered from Machi, a bird that was shot on Guadeloupe in September of 2011).

Map of migration route for three whimbrels that were marked on a breeding ground in western Canada. Incredible flight over the open Atlantic Ocean was previously undocumented.

The three birds are part of a larger project that has included 20 additional birds that have been tracked to better understand migratory pathways and locations that are critical for this declining species. The study has tracked whimbrels for more than 185,000 miles (300,000 kilometers) since 2008. The broader tracking project is a collaborative effort between the Center for Conservation Biology, the Canadian Wildlife Service, the Nature Conservancy, the U.S. Fish and Wildlife Service, Georgia Department of Natural Resources, the Virginia Coastal Zone Management Program and Manomet Center for Conservation Sciences.

Provided by Virginia Commonwealth University

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Scientists identify previously unknown Whimbrel migration pathway over open Atlantic Ocean

Organovo Reports Q2 2012 Financial Results, Provides Business Update

SAN DIEGO, Aug. 15, 2012 /PRNewswire/ --Organovo Holdings, Inc. (ONVO) ("Organovo") a three-dimensional biology company focused on delivering breakthrough 3-D bioprinting technology, today reported unaudited financial results for the period ended June 30, 2012.

(Logo: http://photos.prnewswire.com/prnh/20120813/MM55537LOGO)

Organovo is focused on breakthrough 3D bioprinting technology to create tissue on demand for research and medical applications. The company's NovoGen MMX Bioprinter() is part of a 3D human tissue generation platform that works across a broad array of tissue and cell types to recapitulate in vivo biology. Organovo's bioprinting technology has immediate applications in disease research, drug discovery and development, and toxicology testing. In the future, the Company believes that applications of this technology hold the promise to generate tissues for therapeutic uses.

Second quarter 2012 revenues increased approximately 49% above the same period in 2011. Collaborative research revenues for the second quarter increased approximately 81% over the same period of prior year revenues, but were partiallyoffset by a reduction in grant revenues. Loss from Operations for the second quarter was approximately $1,449,700.

Recent Corporate HighlightsOn July 17, 2012, Organovo announced the commencement of operations at its new, larger facility in San Diego, California. The new facility has over three times the capacity of Organovo's previous headquarters and is expected to facilitate the Company's needs to grow staff and research and development output.

On July 9, 2012, Organovo announced the receipt of two issued patents. The patents consisted of the issuance in the United States of a patent to which the Company owns the exclusive license from the University of Missouri, and the issuance in the United Kingdom of the Company's first assigned patent.

On July 9, 2012 Organovo announced the appointment of James T. Glover, former CFO of Beckman Coulter and Anadys Pharmaceuticals, to its Board of Directors. Mr. Glover has been affirmed as an independent director by the Organovo Board of Directors, and the Company expects to attract additional independent directors as it grows.

On May 21, 2012, Organovo announced the hiring of Dr. Eric Michael David as Chief Strategy Officer.

On April 25, 2012, Organovo announced the hiring of Michael Renard as its Executive Vice President, Commercial Operations, and the promotion of Dr. Sharon Presnell to Chief Technology Officer.

The Company is performing on current contracts with Pfizer and United Therapeutics. The Company expects to book revenue on both contracts in the second half of 2012.

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Organovo Reports Q2 2012 Financial Results, Provides Business Update

Grey's Anatomy(TM) Professional Wear by Barco Signature Series Brings Professional Polish

GARDENA, CA--(Marketwire -08/15/12)- Barco Uniforms, an acclaimed leader in the uniform industry, unveiled its striking new Grey's Anatomy Professional Wear by Barco Signature Series. The collection, with new fabric, colors and designs, builds on the company's most popular styles, adding a professional, "heathered" look and arcLux with stretch, which clothes professionals in luxurious comfort that stretches and flatters every shape and fit.

"Barco Uniforms shares the passion and commitment medical professionals bring to their work every day, and we understand that while their uniforms must be practical, professionals desire comfortable, flattering, professional styles," said David Murphy, Senior Vice President, of Sales and Marketing at Barco Uniforms. "Our new Grey's Anatomy Professional Wear by Barco Signature Series is designed to deliver the ease and performance expected from Barco Uniforms in fashion-forward, sophisticated styles."

The new collection is created from soft, touchable fabrics that stretch to move with the body to deliver professional polish, whether meeting with colleagues, patients or families, handling crises or providing everyday care. Four exciting new colors -- Electric Heather, Punch Heather, Purple Rain Heather and Hot Tamale Heather -- complement Barco's popular Bahama Heather, Black Heather, Cabernet Heather, and Indigo Heather fabulous prints to create the perfect palette for expanding or designing an entirely new wardrobe. Advanced moisture wicking ensures all-day ease, even through the longest and most demanding shifts.

Grey's Anatomy Professional Wear by Barco Signature Series is available now at leading medical uniform retailers. To locate a retail outlet, visit http://medical.barcouniforms.com/medical/locator.asp.

About Barco UniformsBarco Uniforms, a recognized leader in the uniform industry, fuses innovative fabric technology and fashion-forward design to create uniforms that inspire individuals and enhance the work environment. From its versatile, widely appealing Medical Collections and distinctive Spa Collection, to its corporate Identity solutions, Barco Uniforms is committed to making professional attire that people love to wear. For more information, visit http://www.barcouniforms.com/.

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Grey's Anatomy(TM) Professional Wear by Barco Signature Series Brings Professional Polish

Primary looks to strong earnings growth

Medical centres operator and pathology provider Primary Health Care has unveiled a near 50 per cent rise in full year profit and forecast stronger earnings in 2012/12.

Primary lifted its net profit for the year to June 30 by 49 per cent to $116.6 million, from $78.3 million in 2010/11.

Revenue climbed 5.3 per cent to $1.4 billion.

Primary impressed investors by forecasting a 20-25 per cent rise in earnings per share (EPS) in 2012/13.

Its EPS was 23.3 cents a share in 2011/12.

Primary also expects earnings before interest, tax, depreciation and amortisation to climb to $370-380 million in 2012/13, from $351.1 million in 2011/12.

"Primary is able to look forward to strong growth as a result of the underlying strength of the business, positive industry dynamics, and long-term increasing demand for healthcare services," Primary said in a statement on Wednesday.

Shares in the company were 34 cents, or 11 per cent, higher at $3.43 at 1038 AEST.

Primary, which operates 76 medical centres, said it expected consolidation in the industry to continue and would look for small bolt-on acquisitions.

Its medical centres, pathology and medical imaging divisions all lifted their earnings and revenue during 2011/12.

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Primary looks to strong earnings growth

New method to closely model diseases caused by splicing defects

ScienceDaily (Aug. 14, 2012) A team led by scientists at Cold Spring Harbor Laboratory (CSHL) has developed a new way of making animal models for a broad class of human genetic diseases -- those with pathology caused by errors in the splicing of RNA messages copied from genes. To date, about 6,000 such RNA "editing" errors have been found in various human illnesses, ranging from neurodegenerative disorders to cancer.

The new modeling approach can provide unique insights into how certain diseases progress and is likely to boost efforts to develop novel treatments. It was tested successfully by the CSHL team, led by Professor Adrian Krainer, Ph.D., in collaboration with scientists from Isis Pharmaceuticals, in mouse analogs of human spinal muscular atrophy (SMA), a motor-neuron disease that is the leading genetic cause of childhood mortality. The results are detailed in a study published August 15 in Genes & Development.

The modeling method is called TSUNAMI (shorthand for targeting-splicing using negative ASOs to model illness). The study demonstrates it can be used in illnesses with pathology associated with the missplicing of pre-mRNAs -- unedited RNA molecules that bear the messages encoded in genes which provide instructions for cells to manufacture specific proteins.

Correcting splicing errors in SMA

A cellular machine called the spliceosome routinely snips non-essential bits called "introns" out of every pre-mRNA molecule that carries a copy of a gene's instructions. All that should remain after the spliceosome has done its work is a string of spliced-together "exons," the protein-encoding portions of the message. These edited mRNA messages are subsequently read by ribosomes, the cellular factories where proteins are synthesized.

In SMA and some other human illnesses, pathology can be traced to errors in the pre-mRNA editing process. In SMA, it is caused either by a severe mutation in a gene called SMN1 ("survival of motor neuron-1") or by that gene's complete absence in an affected individual's genetic material. The SMN protein normally encoded by the gene is essential for motor neuron development. Humans have a second, similar gene called SMN2, but it is a poor backup. Because of an error in the splicing of its pre-mRNA, the SMN2 gene, when expressed, typically produces only a fraction of the SMN protein needed by motor neurons. This is critical in the first stages of life when the body and muscles are still developing.

While the level of the "backup" gene's protein output varies in individuals with spinal muscular atrophy, resulting in pathology of varying intensity, Krainer -- a leading expert on splicing -- and his collaborators have succeeded in recent years in devising a method of getting SMN2 to produce therapeutic amounts of protein, enough to reverse pathology in both mild and severe mouse analogs of the disorder.

To achieve this they synthesized tiny snippets of RNA called ASOs (antisense oligonucleotides) and injected them into the cerebrospinal fluid of mice carrying a human SMN2 transgene (i.e., a gene not native to mice). This enabled them to get the therapeutic ASOs through the so-called blood-brain barrier, to reach cells throughout the central nervous system. ASOs are configured to attach at highly specific spots in pre-mRNAs, where, by design, they can inhibit activators or repressors of the splicing process. Krainer's team synthesized an ASO that corrected the SMN2 splicing error and gave rise to therapeutic amounts of SMN protein. Importantly, the ASO was shown to be stable in the body as well as persistent, the effects of a single injection lasting at least half a year in mice.

TSUNAMI's 'negative ASOs': therapy in reverse

A version of this therapeutic ASO is now being tested in Phase 1 human trials. But even as the tests proceed, Krainer and colleagues have worked on getting the splice-correction method to work in reverse: using a "negative ASO" to cause or exacerbate disease pathology in neonatal mice, with the approach they call TSUNAMI.

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New method to closely model diseases caused by splicing defects

Starkville nutrition store owner helps clients find their 'want to'

Chris Williams, owner of Peak Nutrition, originally planned to enter law school or pursue a career in politics but his own struggle with weight led him to open his own nutrition store in Starkville. Photo by: Micah Green/Dispatch staff

If you had asked Chris Williams where he thought he would be at 23 years old, he probably would have told you he would be in law school or working in the political arena. Instead, the former football player turned entrepreneur has opened his own nutritional shop in Starkville.

Truly one of a kind to the area, Peak Nutrition focuses on the body and the mind. Williams opened the store last week and said he already has customers lining up to try the shakes made in house and the meal plans targeted to athletes on the go.

Williams said that before anyone can begin to get in shape, they first must have the desire or as he commonly calls it, "the want to."

He said he had that break through moment several months back. Williams played football all throughout high school and college, first as a tight end and then as a defensive tackle. Williams said he quickly gained weight when playing, starting out at less than 220 pounds and to 278 pounds by his senior year. When he graduated from Mississippi College in December 2011, he quit playing football, but kept consuming the same amount of calories as when he was working out on the field. Williams said he knew he needed to lose weight but didn't know where to start. Not only was he becoming unhappy with his weight, Williams was also beginning to question the direction his professional life was going as well. That is when he said he had that "want to" moment and approached a friend to help him lose weight. Williams began eating right and leading an active lifestyle, focusing not only on his physical health, but his mental health as well. He quickly began losing weight but in addition, his state of mind changed, too. He said he had more energy and was on overall happier person.

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Starkville nutrition store owner helps clients find their 'want to'