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Singer Sarah Brightman Outbids NASA for Space Tourist's Seat
Posted: October 3, 2012 at 9:19 pm
What's a rich space tourist to do? If you want to fly in space, seats are harder to find than a flight out of Chicago's O'Hare airport during a blizzard. So your only option is to bump an astronaut from a seat on a Russian Soyuz spacecraft going to the International Space Station.
ABC News has learned that singer Sarah Brightman, of "Phantom of the Opera" fame, will be the next tourist in space, sometime in 2014 or 2015. To get her seat she had to pay the Russian space agency more than the $51 million NASA budgets on average to send its astronauts to the station.
To maintain its presence in orbit when Soyuz seats are limited, NASA had to agree to commit at least one of its astronauts to spend a year in space, instead of the six months they currently stay. Brightman's trip will be announced in Moscow on Oct. 10.
NASA says a year in space has great medical research benefits. Astronauts spending just six months on the space station in the past have suffered from radiation exposure, muscle mass loss, decreased bone density, and vision problems. The research from a year on the space station will help NASA plan for long flights to Mars or an asteroid. It does mean an astronaut will get booted from a flight to adjust for one less seat.
When the space shuttle quit flying last year, it created a conundrum for companies like Space Adventures, whose business -- sending rich tourists into space -- depended upon the resources of Roscosmos, the Russian space agency. Roscosmos is the only space agency willing to send tourists to space. NASA won't do it, and now they don't have a spacecraft anyway so it's a moot point.
Don't have $50 million to spare? There is a budget option: $200,000 for a suborbital flight on Virgin Galactic' s SpaceshipTwo, which should start commercial flights in a couple of years. SpaceShipTwo is designed to be a six-passenger, two-pilot craft, flying to the edge of space. The flight will be short -- just six minutes of weightlessness, but passengers will be able to unbuckle and float around the cabin. If you have $1 million to spare, you can book one trip for yourself and a few friends.
Boeing would like to get into the space tourism business as well, partnering with Space Adventures at some point to launch from Florida.
Space Adventures offers ten days on the International Space Station, in low Earth orbit, with great views and not-so-great accommodations. But there is zero gravity, which means you get to do somersaults and float as much as you want. For a singer like Sarah Brightman, who thrilled the world when she starred in "Phantom of the Opera," the inspiration should be out of this world.
Rumors flew earlier this week when author J.K. Rowling told an audience in England she had once been offered a seat on a space shuttle for a couple of million dollars. NASA quickly scotched that story.
Space Adventures has flown seven tourists into space since 2000. Clients have paid from $22 million to $35 million in the past, but the limited number of Soyuz seats drove the price to more than $50 million. After all, if NASA is willing to pay $51 million, Russia doesn't need to sell the seat at half price.
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Does moral decision-making in video games mirror the real world?
Posted: at 9:19 pm
Public release date: 3-Oct-2012 [ | E-mail | Share ]
Contact: Vicki Cohn vcohn@liebertpub.com 914-740-2100 Mary Ann Liebert, Inc./Genetic Engineering News
New Rochelle, NY, October 3, 2012Making moral judgments is increasingly a central element of the plots of popular video games. Do players of online video games perceive the content and characters as real and thus make moral judgments to avoid feeling guilty? Or does immoral behavior such as violence and theft make the game any more or less enjoyable? The article "Mirrored Morality: An Exploration of Moral Choice in Video Games" published in Cyberpsychology, Behavior, and Social Networking, a peer-reviewed journal from Mary Ann Liebert, Inc., publishers examines these types of questions. The article is available free online on the Cyberpsychology, Behavior, and Social Networking website.
Andrew Weaver and Nicky Lewis, Indiana University, Bloomington, studied how players make moral choices in video games and what effects those choices have on their emotional responses to the games. In general, players tended to make "moral" decisions and to treat game characters as though they were actual people. Although behaving in antisocial ways was associated with greater guilt, it did not affect player enjoyment.
"Although preliminary, these results point to the utility of games as teaching and educational tools, as well as important tools for the assessment of behavior," says Brenda K. Wiederhold, PhD, MBA, BCIA, Editor-in-Chief of Cyberpsychology, Behavior, and Social Networking, from the Interactive Media Institute, San Diego, CA. "These findings indicate how real the virtual world can become when one suspends disbelief and immerses oneself in the scenario."
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About the Journal
Cyberpsychology, Behavior, and Social Networking is an authoritative peer-reviewed journal published monthly in print and online that explores the psychological and social issues surrounding the Internet and interactive technologies. Complete tables of content and a sample issue may be viewed online on the Cyberpsychology, Behavior, and Social Networking website.
About the Publisher
Mary Ann Liebert, Inc., publishers is a privately held, fully integrated media company known for establishing authoritative peer-reviewed journals in many promising areas of science and biomedical research, including Games for Health Journal, Telemedicine and e-Health, and Journal of Child and Adolescent Psychopharmacology. Its biotechnology trade magazine, Genetic Engineering & Biotechnology News (GEN), was the first in its field and is today the industry's most widely read publication worldwide. A complete list of the firm's 70 journals, books, and newsmagazines is available on the Mary Ann Liebert, Inc., publishers website.
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Animals engineered with pinpoint accuracy
Posted: at 9:19 pm
A cow in New Zealand has been genetically modified to produce hypoallergenic milk.
AgResearch
Two genetically engineered farm animals reported today illustrate how far from Frankensteins stitched-together monster animal biotechnology has come. One of those animals, a cow, secretes milk that lacks an allergy-inducing protein because researchers accurately blocked its production using the technique of RNA interference1. And in pigs, scientists have used an enzyme called a TALEN2 to scramble a gene that would normally help remove cholesterol.
RNA interference (RNAi) and TALENs are more accurate at targeting the gene in question than are earlier genetic engineering techniques. For years, researchers tried to remove the allergy-inducing milk protein beta-lactoglobulin from cow's milk, which can cause diarrhea and vomiting in some toddlers. They tried replacing the gene encoding beta-lactoglobulin with a defective form, but this proved nearly impossible because the techniques available to introduce foreign genes into animal genomes were not precise, and misplaced genes failed to express themselves correctly.
In 2006, scientists at AgResearch in Hamilton, New Zealand began to experiment with molecules that interfere with the messenger RNA go-between that enables translation of a gene into protein. In mice, they discovered a short chunk of RNA, called a microRNA, that targeted beta-lactoglobulin messenger RNA directly to prevent its translation. They inserted DNA encoding a version of this microRNA into the genome to create genetically modified cow embryos that they hoped would grow into cows without the allergen in their milk. Out of 100 embryos, one calf yielded beta-globulin-free milk. This isnt a quick process, says Stefan Wagner, a molecular biologist at AgResearch. That's why it has taken so long to succeed in making an allergen-free cow, he says.
Wagner says that TALENs, which were not readily available when he began his research, might speed up the process, and that the team plans to use them to eliminate beta-lactoglobulin. RNAi cannot eliminate the protein completely because some messenger RNA slips past the blockade, but each TALEN targets a specific DNA sequence in the genome and cuts it. As the body repairs the break, mutations are often introduced that render the targeted gene non-functional. The TALEN technology is staggeringly easy, quick, and leaves no mark in the genome, says Bruce Whitelaw, a molecular biologist at the Roslin Institute near Edinburgh in the United Kingdom, who contributed to the work in pigs. In essence, we are just mimicking an evolutionary process with precise, man-made editors.
His team used TALENs to disrupt genes encoding low-density lipoprotein (LDL) receptors. Without these receptor proteins to remove cholesterol-containing LDLs from the blood, LDLs build-up and lead to atherosclerosis. Pigs with this condition may be reliable models of human atheroscelerosis in biomedical research.
The TALEN-modified pig is not the first model of human heart disease (see Model pigs face a messy path), but the technique makes genetic engineering less costly and more efficient. Id be exaggerating if I said that pigs and cows can now be thought of as big mice, but we are moving in that direction, says Heiner Niemann, a bioengineer at the Institute of Farm Animal Genetics in Neustadt, Germany.
The excitement surrounding these technological advances is bittersweet, however. Originally, engineered animals were produced with the aim of making food safer, healthier and more abundant. Yet despite years of investment, almost no animal has been approved by regulatory agencies around the world. Wagner says he has not tasted the milk from his special cow because hes not permitted to under New Zealand law. We must restrict our research to scientific analysis, he says. The current climate for animal biotech is not very good, and therefore, we are nowhere near getting this to the consumer."
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Cellectis Publishes Results Paving the Way for New Therapeutic Approaches against Cancer and Genetic Diseases
Posted: at 9:19 pm
PARIS--(BUSINESS WIRE)--
Regulatory News:
Cellectis (ALCLS.PA), the French genome engineering specialist, announces in the Journal of Biological Chemistry, one of the most respected scientific journals in the world, the publication of a new approach regarding the targeted modification of DNA2. The manuscript unmasks novel perspectives and broadens the scope of TALENsTM technology to new therapeutic approaches to fight against cancer and genetic diseases. Until now, TALENsTM, the molecular scissors created by Cellectis Group, were only able to target certain parts of the genome. A team of the Groups researchers, led by Julien Valton and Philippe Duchateau, was able to overcome this constraint, opening the way to a wider range of applications, especially in the therapeutic field.
This study, the first to be published on TALENsTM, was awarded by the selection committee of the JBC as Paper of the Week.
Since their identification in 2009, TALEs have quickly emerged as the new generation of DNA-binding domain with programmable specificity and have been successfully used to generate the molecular scissors known as TALENsTM. However, their sensitivity to methylation, a ubiquitous modification of DNA, represents a major bottleneck for their widespread utilization in the genome engineering and therapeutic fields. Using a combination of biochemical, structural and cellular approaches, the R&D department of Cellectis was able to identify the basis of such sensitivity and more importantly, to propose an efficient and universal method to overcome it.
These results are proof of the scientific creativity and quality of our research teams, as well as the power of our genome engineering tools. This new publication strengthens the relevance of our investment in TALEstechnology, and confirms our strategy within the therapeutic field, declared Andr Choulika, Chief Executive Officer of Cellectis Group.
2) Overcoming TALE DNA Binding Domain Sensitivity to Cytosine Methylation Julien Valton, Aurelie Dupuy, Fayza Daboussi, Severine Thomas, Alan Marechal, Rachel Macmaster, Kevin Melliand, Alexandre Juillerat and Philippe Duchateau J. Biol. Chem. jbc.C112.408864. First Published on September 26, 2012, doi:10.1074/jbc.C112.408864
About Cellectis
Founded in France in 1999, the Cellectis Group is based on a highly specific DNA engineering technology. Its application sectors are human health, agriculture and bio-energies. Co-created by Andr Choulika, its Chief Executive Officer, Cellectis is today one of the world leading companies in the field of genome engineering. The Group has a workforce of 230 employees working on 5 sites worldwide: Paris & Evry in France, Gothenburg in Sweden, St Paul (Minnesota) & Cambridge (Massachusetts) in the United States. Cellectis achieved in 2011 16M revenues and has signed more than 80 industrial agreements with pharmaceutical laboratories, agrochemical and biotechnology companies since its inception. AFM, Dupont, BASF, Bayer, Total, Limagrain, Novo Nordisk are some of the Groups clients and partners.
Since 2007, Cellectis has been listed on NYSE-Euronext Alternext market (ALCLS.PA) in Paris.
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Free Engine
Posted: at 9:19 pm
According to UC Berkeley professor Ignacio Chapela, the passage of Proposition 37 will not only restore the right to choose what foods we put in our bodies, but it may restore scientific process to its rightful placesomething the bioengineering industry, with full assistance from the White House, removed.
"The promises made by genetic engineering have not been fulfilled," explains Chapela, a microbial biologist who was first to exposed the fact that genetically engineered corn was contaminating ancient strains of Mexican maize via cross-pollinating. "Genetic engineering has proven to be wishful thinking, a dream that has failed."
Chapela considers himself fortunate to be able to speak out freely about GMO failings, since so many other scientists have been attacked or threatened or have lost employment for approaching genetic engineering with a critical eye. "I would like to speak for those scientists," says Chapela, "because they cannot." When the first Bush administration instructed federal regulatory bodies to step aside and give the GE industry free reign, Chapela explains, there was no scientific scrutiny allowed.
"It has been very hard to survive as a scientist who is a critical thinker now," Chapela says. "The central dogma embedded in K-12 science textbooks indoctrinates young people to accept that genetic engineering is an inevitable part of life. It says all living things are driven by genes encoded in DNA, and that by manipulating that DNA we can create life, and mix, match and alter it the way we want it." But this isn't the way it actually plays out, says Chapela. "The reality is that genetic engineering is not working, any way you look at it."
What Proposition 37 offers consumers is the promise that all GMO foods will be labeled in California. What it offers scientists is a chance to scrutinize an industry that has intimidated themsometimes to the point of ruining their careersfor questioning the validity of genetic engineering. "The Bush administration decided in the 1980s that genetic engineering was the next wave of economic development for the U.S. and for the world," says Chapela. "We were instructed to look the other way."
Labeling GE foods may help science, which at present cannot investigate whether GE food consumption is related to rises in disease. "We have been sitting here in the dark, forbidden from looking," says Chapela, who believes a GMO-labeling law will give us "the simple capacity to know and to do the science for the first time. I think we deserve it."
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The GM Barnyard
Posted: at 9:19 pm
Allergen-free cows milk and pigs with hardened arteries illustrate how the accuracy of genetic engineering has improved.
Two unsuspecting farm animals have helped to demonstrate the increasing accuracy of genetic engineering techniques. The first is a cow that produced hypoallergenic milk after researchers used RNA interference to block the production of an allergy-inducing protein, as reported this week (October 2) in Proceedings of the National Academy of Sciences. The second, reported in another paper in the same issue, is a pig that could be a model for atherosclerosis after researchers used an enzyme called a TALEN to silence a gene that helps to remove cholesterol.
Researchers have long struggled to remove cow milks allergy-inducing protein, beta-lactoglobulin, which can cause diarrhea and vomiting in children. They were previously unable to introduce foreign genes precisely enough, however, so they could never quite successfully replace the gene that codes for beta-lactoglobulin with a defective form.
But scientists at AgResearch in Hamilton, New Zealand, worked with molecules that interfere with messenger RNA (mRNA), which helps translate genes into proteins. They found microRNA (miRNA) in mice that targeted beta-lactoglobulin mRNA, so they inserted DNA encoding a version of this miRNA into the genomes of cow embryos. Out of 100 embryos, one calf produced beta-globulin-free milk. This isnt a quick process, Stefan Wagner, a molecular biologist at AgResearch, told Nature. One problem is that RNA interference cant eliminate the protein completely because some mRNA slips through.
Another technique could speed up the process. TALENs are enzymes that target and cut out a specific DNA sequence from the genome. As the break is repaired, mutations are introduced that scramble the targeted gene, leaving it unable to function.
The TALEN technology is staggeringly easy, quick, and leaves no mark in the genome, researcher Bruce Whitelaw, told Nature. Whitelaw, a molecular biologist at the Roslin Institute near Edinburgh, United Kingdom, used TALENs to disrupt genes encoding low-density lipoprotein (LDL) receptors in pigs. Without those receptors, which remove LDL from the blood, Whitelaws pigs develop atherosclerotic arteries. Such pigs could be reliable models for biomedical researchers studying human atherosclerosis.
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Myriad Genetics Sponsors Cancer Awareness Initiatives in Support of National Hereditary Breast and Ovarian Cancer Week
Posted: at 9:19 pm
SALT LAKE CITY, Oct. 3, 2012 (GLOBE NEWSWIRE) -- Myriad Genetics, Inc. (MYGN) today announced that, in support of National Hereditary Breast and Ovarian Cancer (HBOC) Week and National Previvor Day, it has launched an online quiz to help people assess their risk for hereditary cancers. The Hereditary Cancer Quiz is available online at http://www.hereditarycancerquiz.com. In addition, the company is providing financial support toward educational and awareness initiatives to three advocacy organizations-Bright Pink, the National Ovarian Cancer Coalition (NOCC) and Living Beyond Breast Cancer (LBBC).
HBOC Week marks the transition between National Ovarian Cancer Awareness Month and National Breast Cancer Awareness Month and was established by U.S. Congressional resolution in 2010 to raise awareness about hereditary cancer. National Previvor Day raises awareness for those individuals who have a known gene mutation or a strong family history of cancer but have not yet developed cancer.
"Understanding their risk for hereditary cancers, such as breast and ovarian cancer, is critical to helping patients make informed decisions about treatment and prevention. Our hereditary cancer risk quiz empowers patients to understand their family history and provides a framework for an informative discussion with a healthcare professional," said Mark Capone, President, Myriad Genetic Laboratories. "In addition, organizations such as Bright Pink, NOCC and Living Beyond Breast Cancer offer hereditary cancer patients and their families vital support and information in their fight against these diseases, and we are proud to support their efforts."
"Funding from Myriad and our other partner companies assists our organization in offering better and more valuable resources to hereditary cancer patients and their families," said David Barley, Chief Executive Officer, National Ovarian Cancer Coalition. "We are proud to work with Myriad, as they play a major role in the understanding and diagnosis of a person's hereditary risk for cancer."
About Hereditary Cancer
Hereditary cancers, also called inherited cancers, are those caused by genetic mutations that are passed from parent to child. These mutations predispose people to developing a particular type of cancer. Mutations in BRCA1 and BRCA2 genes are the most common cause of hereditary breast and ovarian cancers and can lead to male breast cancer, pancreatic cancer, prostate cancer and others. Women with a BRCA mutation are five times more likely to develop breast cancer than those without the mutation and more than ten times as likely to develop ovarian cancer1. Approximately 7%2 of breast cancer and approximately 14% 3,4,5 of invasive ovarian cancer result from inherited gene mutations.
DNA testing for BRCA mutations is done through a blood or saliva test and can indicate whether a person carries a BRCA gene mutation. Testing is recommended for people with certain personal and/or family history pattern, including:
Myriad Genetics is a pioneer in hereditary cancer testing and offers tests for a variety of hereditary cancer syndromes, including BRACAnalysis(R), which detects mutations in the BRCA1 and BRCA2 genes. This test has become the standard of care in identification of individuals with hereditary breast and ovarian cancer. Nearly one million patients have benefited from Myriad's hereditary cancer testing.
About Myriad Genetics
Myriad Genetics is a leading molecular diagnostic company dedicated to making a difference in patients' lives through the discovery and commercialization of transformative tests to assess a person's risk of developing disease, guide treatment decisions and assess risk of disease progression and recurrence. Myriad's portfolio of molecular diagnostic tests are based on an understanding of the role genes play in human disease and were developed with a commitment to improving an individual's decision making process for monitoring and treating disease. Myriad is focused on strategic directives to introduce new products, including companion diagnostics, as well as expanding internationally. For more information on how Myriad is making a difference, please visit the Company's website: http://www.myriad.com
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Myriad Genetics Sponsors Cancer Awareness Initiatives in Support of National Hereditary Breast and Ovarian Cancer Week
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Study Says Genetics Of Intelligence Remains A Riddle, For Now
Posted: at 9:19 pm
October 3, 2012
April Flowers for redOrbit.com Your Universe Online
Your intelligence like almost all other traits is a gift from your parents, at least in part. Scientists have known for a long time that intelligence is at least partially inherited through genetics. According to psychological scientist Christopher Chabris, however, it may be some time before researchers can identify the specific genetic roots of intelligence.
A new study from Union College shows that the genes long thought to be linked to intellectual prowess actually appear to have no bearing on ones IQ, complicating scientific endeavors to get to the root of the genetics of intelligence.
An international team of researchers including Harvard economist David Laibson used large data sets that included both intelligence testing and genetic data to examine a dozen genes. In almost every case, the team found that IQ could not be linked to the specific genes that were tested.
In all of our tests we only found one gene that appeared to be associated with intelligence, and it was a very small effect. This does not mean intelligence does not have a genetic component. It means its a lot harder to find the particular genes, or the particular genetic variants, that influence the differences in intelligence, said Chabris. The results of this new study were published online in the journal Psychological Science.
Previous studies of identical and fraternal twins informed and bolstered the notion that intelligence is a heritable trait. This new research validates that conclusion, yet the exact parameters of the genetics of intelligence remain a mystery. The team asserts that the older studies, which picked out specific genes, had flaws because of the technological limits of the time. Those limits prevented researchers from probing more than a few locations in the human genome to find genes that affected intelligence.
We want to emphasize that we are not saying the people who did earlier research in this area were foolish or wrong, Chabris said. They were using the best technology and information they had available. At the time, it was believed that individual genes would have a much larger effect they were expecting to find genes that might each account for several IQ points.
The team says that much more research is needed to determine the exact role that genes play in intelligence.
As is the case with other traits, like height, there are probably thousands of genes and their variants that are associated with intelligence, he said. And there may be other genetic effects beyond the single gene effects. There could be interactions among genes, or interactions between genes and the environment. Our results show that the way researchers have been looking for genes that may be related to intelligence the candidate gene method is fairly likely to result in false positives, so other methods should be used.
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DNA construction technology makes genetic engineering cheaper, faster
Posted: at 9:19 pm
Sequencing, splicing and expressing DNA may seem to be the quintessence of cutting-edge scienceindeed DNA manipulation has revolutionized fields such as biofuels, chemicals and medicine. But in fact, the actual process can still be tedious and labor-intensive, something Lawrence Berkeley National Laboratory (Berkeley Lab) scientist Nathan Hillson learned the hard way.
After struggling for two days to design a protocol to put together a genetic circuit with 10 pieces of DNAusing a spreadsheet as his primary toolhe was dismayed to discover that an outside company could have done the whole thing, including parts and labor, for lower cost than him ordering the oligonucleotides himself. "I learned two things: one, I never wanted to go through that process again, and two, it's extremely important to do the cost-effectiveness calculation," said Hillson, a biochemist who also directs the synthetic biology program at the Berkeley Lab-led Joint BioEnergy Institute (JBEI). "So that was the genesis of the j5 software. This is the perfect thing to teach a computer to do."
The j5 software package, which has attracted users from more than 250 institutions worldwide since it was made available last year, is now the basis for the latest startup to emerge from JBEI, a Department of Energy research center established in 2007 to pursue breakthroughs in the production of cellulosic biofuels. By building on j5 and adding modules for commercial users, TeselaGen Biotechnology, founded by Hillson and two partners, says it will significantly reduce the time and cost involved with DNA synthesis and cloning, a multibillion-dollar market.
"It's like AutoCAD for biology," said TeselaGen co-founder and CEO Mike Fero. "Modern cloning is a computational problem. We are the missing informatic piece to making modern scarless DNA assembly methods a reality for the majority of biologists. Otherwise it's a small cadre of people who can do it."
Recombinant DNA assemblies are critical tools in a number of scientific pursuits: for understanding how cells are altered in diseases such as cancer, for building better antibiotics, for converting plant biomass to biofuels and for basic scientific understanding of cellular pathways. Standard cloning techniques have been in use for 40 years and are still the industry standard.
"Our biggest competition is traditional cloning, or inertia," said Fero, who was a particle physicist for 10 years before pursuing a career in biotech. "We have to make it so easy people will happily switch to the newer methods."
TeselaGen licensed j5 from Berkeley Lab, the lead institutional partner of JBEI, and currently has more than 100 scientists and engineers from large industrial and pharmaceutical companies in private beta.
"We are so pleased with the startup of TeselaGen, based on a deceptively simple idea but clearly providing a solution to a very difficult problem," said Cheryl Fragiadakis, director of technology transfer at Berkeley Lab. "It is a great example as well of a company coming out of our JBEI activities.The Lab's Tech Transfer encourages and supports entrepreneurial ventures, providing education and networking for our scientists, as a great way to get technologies out for the benefit of society."
The cloud-based software not only designs DNA construction protocols, it will compare methods to determine the one that is most cost-effective, weighing, for example, if it is cheaper to outsource a portion of the DNA construction.The more complex the task, the more time and money the program can save. The greatest savings are with combinatorial libraries, collections of hundreds to millions of related DNA assemblies, each with a different combination of genes or parts that perform similar functions in different organisms.
For example, simple construction of a metabolic pathway that takes two and a half weeks and costs $1,400 using traditional cloning can be cut down to two weeks and less than half the cost with j5. A more complex task of constructing a combinatorial protein library (with 243 constructs) would drop from $122,000 and 11 months with traditional cloning to under $30,000 and 1.5 months with j5. The same task using direct DNA synthesis would cost $538,000 and take 2.3 months.
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DNA Helps Locate Cold Case Murder Suspect
Posted: at 9:19 pm
October 3, 2012 Updated Oct 3, 2012 at 2:52 PM EDT
Miami County, Ind. (Indianas NewsCenter) DNA evidence plays a key role in helping authorities make an arrest in a 20-year-old murder case.
The Miami County Prosecutors Office announced Wednesday Timothy J. Jimerson of Biloxi, Mississippi was arrested in connection to the cold case murder of Toni Spicer, who was found murdered in her mobile home in the southern part of Miami County, all thanks to DNA evidence collected 20 years ago.
Prosecutor Bruce Embrey says that due to the very detailed and thorough crime scene investigation performed by Sgt. Dean Marks and State Trooper Gary Boyles in 1992, police agencies at any time could help in the murder investigation.
The evidence collected from the scene was sent off for DNA examination and cataloging, awaiting a DNA hit so that a suspects name could be issued. But it wasnt until recently that a DNA match was found.
Since a DNA match in most cases isnt enough to identify a suspect, the help of the Biloxi, Mississippi Police Department was enlisted and after extensive investigation Jimerson was arrested and is now awaiting extradition back to Peru.
Copyright 2012 A Granite Broadcasting Station. All rights reserved. This material may not be published, broadcast, rewritten or redistributed.
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DNA Helps Locate Cold Case Murder Suspect
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