Daily Archives: February 23, 2015

COD Advanced Warfare: DNA BOMB & Supply Drops #1 – Video

Posted: February 23, 2015 at 10:44 pm


COD Advanced Warfare: DNA BOMB Supply Drops #1
In this video I get a DNA Bomb on the new maps of call of duty advanced warfare it was awesome it is like a Nuke like back in the days but anyway I do show off some Supply Drops and it was...

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COD Advanced Warfare: DNA BOMB & Supply Drops #1 - Video

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Police turn to new DNA-powered technology in hopes of finding killer

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By Melody Schreiber February 23 at 2:57 PM

Four years ago, Candra Alston and her 3-year-old daughter, Malaysia Boykin, were murdered inside their South Carolina apartment. Police in Columbia collected DNA at the scene, but the investigation stalled.

Prime-time crime shows would have you believe DNA samples can convict the guilty and clear the innocent, but real life is more complicated. In order to find an assailant, the DNA has to match either a previous offender in the FBIs CODIS database or a sample from one of the victims acquaintances. When it doesnt, the investigation hits a wall. In the South Carolina case, police gathered 150 DNA samples and conducted 200 interviews with likely suspects and still nothing.

Now the Columbia police are experimenting with a new technology that uses tiny amounts of DNA to create a computer-generated illustration of their suspect. Snapshot, a program developed by a Reston, Va., company called Parabon NanoLabs, goes beyond simply listing physical attributes eye color, hair color, ethnicity and facial features and creates a 3-D image of what the killer might look like. The police in South Carolina hope that publicly releasing the suspects image and description will bring up fresh leads in a stale case.

Dabrien Dabe Murphy, the senior solutions architect at Parabon, sits in front of three monitors in a little office on the fourth floor of an unremarkable Reston office building not exactly the first place that comes to mind when you think of a lab. With a few keystrokes, Murphy brings up a revolving 3-D image the back of a head. Another few taps and a face attaches itself along the hairline. The face is a mans: olive skin, greenish eyes, full lips.

Murphy has fed DNA markers, linked to certain facial attributes, into 3-D imaging software to create what he calls a composition. It produces a somewhat distorted image where the face meets the rest of the 3-D model.

Theres a little bit of, okay, manual manipulation to make this not look quite so Frankensteined, Murphy explains. Using his cursor to adjust points and axes in the imaging software, Murphy smooths out the hairline and jaw where the projected face attaches itself to the head.

According to the markers Murphy feeds into the imaging software, the man on the screen is of Northwest African ancestry, with hazel or green eyes; black or brown hair; and few or no freckles. This mans DNA was publicly available, so theyre using it to test their model; they know, from the data included with the DNA, that he is Algerian. The trait predictions come with varying levels of confidence; Parabons scientists are 73.4 percent sure that their skin color prediction is accurate, but they are 94.7 percent confident in the subjects eye color.

All this from 9.6 nanograms of DNA. Thats less than 0.00000001 grams, an amount so small, its hard to compare to anything else.

Snapshot combs through a genotype, searching for significant markers and clusters that might indicate physical attributes and removing unimportant variables.

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Police turn to new DNA-powered technology in hopes of finding killer

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Building Face, and a Case, on DNA

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The New York Times; Images and renderings by Mark D. Shriver/Penn State University Individuals' faces compared with Dr. Shriver's computer-generated DNA predictions. See more comparisons.

There were no known eyewitnesses to the murder of a young woman and her 3-year-old daughter four years ago. No security cameras caught a figure coming or going.

Nonetheless, the police in Columbia, S.C., last month released a sketch of a possible suspect. Rather than an artists rendering based on witness descriptions, the face was generated by a computer relying solely on DNA found at the scene of the crime.

It may be the first time a suspects face has been put before the public in this way, but it will not be the last. Investigators are increasingly able to determine the physical characteristics of crime suspects from the DNA they leave behind, providing what could become a powerful new tool for law enforcement.

Already genetic sleuths can determine a suspects eye and hair color fairly accurately. It is also possible, or might soon be, to predict skin color, freckling, baldness, hair curliness, tooth shape and age.

Computers may eventually be able to match faces generated from DNA to those in a database of mug shots. Even if it does not immediately find the culprit, the genetic witness, so to speak, can be useful, researchers say.

That at least narrows down the suspects, said Susan Walsh, an assistant professor of biology at Indiana University-Purdue University Indianapolis who recently won a $1.1 million grant from the Department of Justice to develop such tools.

But forensic DNA phenotyping, as it is called, is also raising concerns. Some scientists question the accuracy of the technology, especially its ability to recreate facial images. Others say use of these techniques could exacerbate racial profiling among law enforcement agencies and infringe on privacy.

This is another of these areas where the technology is ahead of the popular debate and discussion, said Erin Murphy, a professor of law at New York University.

DNA, of course, has been used for more than two decades to hunt for suspects or to convict or exonerate people. But until now, that meant matching a suspects DNA to that found at the crime scene, or trying to find a match in a government database.

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Building Face, and a Case, on DNA

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Customized DNA rings aid early cancer detection in mice, study finds

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Imagine: You pop a pill into your mouth and swallow it. It dissolves, releasing tiny particles that are absorbed and cause only cancerous cells to secrete a specific protein into your bloodstream. Two days from now, a finger-prick blood sample will expose whether you've got cancer and even give a rough idea of its extent.

That's a highly futuristic concept. But its realization may be only years, not decades, away.

Stanford University School of Medicine investigators administered a customized genetic construct consisting of tiny rings of DNA, called DNA minicircles, to mice. The scientists then showed that mice with tumors produced a substance that tumor-free mice didn't make. The substance was easily detected 48 hours later by a simple blood test.

A paper describing the findings of this proof-of-principle study will be published online Feb. 23 in the Proceedings of the National Academy of Sciences.

The technique has the potential to apply to a broad range of cancers, so someday clinicians might be able not only to detect tumors, monitor the effectiveness of cancer therapies and guide the developments of anti-tumor drugs, but -- importantly -- to screen symptom-free populations for nascent tumors that might have otherwise gone undetected until they became larger and much tougher to treat.

Triggering an unambiguous biomarker

The hunt for cancer biomarkers -- substances whose presence in an individual's blood or urine flags a probable tumor -- is nothing new, said the study's senior author, Sanjiv "Sam" Gambhir, professor and chair of radiology and director of the Canary Center at Stanford for Cancer Early Detection. High blood levels of prostate-specific antigen, for example, can signify prostate cancer, and there are also biomarkers that sometimes signal ovarian and colorectal cancer, he said.

But while various tumor types naturally secrete characteristic substances into the blood, the secreted substance is typically specific to the tumor type, with each requiring its own separate test. Complicating matters, these substances are also quite often made in healthy tissues, so a positive test result doesn't absolutely mean a person actually has cancer. Or a tumor -- especially a small one -- simply may not secrete enough of the trademark substance to be detectable.

Gambhir's team appears to have found a way to force any of numerous tumor types to produce a biomarker whose presence in the blood of mice unambiguously signifies cancer, because none of the rodents' tissues -- cancerous or otherwise -- would normally be making it.

This biomarker is a protein called secreted embryonic alkaline phosphatase. SEAP is naturally produced in human embryos as they form and develop, but it's not present in adults.

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Customized DNA rings aid early cancer detection in mice, study finds

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New technology generates photo illustration from a persons DNA

Posted: at 10:44 pm

By Melody Schreiber February 23 at 2:57 PM

Four years ago, Candra Alston and her 3-year-old daughter, Malaysia Boykin, were murdered inside their South Carolina apartment. Police in Columbia collected DNA at the scene, but the investigation stalled.

Prime-time crime shows would have you believe DNA samples can convict the guilty and clear the innocent, but real life is more complicated. In order to find an assailant, the DNA has to match either a previous offender in the FBIs CODIS database or a sample from one of the victims acquaintances. When it doesnt, the investigation hits a wall. In the South Carolina case, police gathered 150 DNA samples and conducted 200 interviews with likely suspects and still nothing.

Now the Columbia police are experimenting with a new technology that uses tiny amounts of DNA to create a computer-generated illustration of their suspect. Snapshot, a program developed by a Reston, Va., company called Parabon NanoLabs, goes beyond simply listing physical attributes eye color, hair color, ethnicity and facial features and creates a 3-D image of what the killer might look like. The police in South Carolina hope that publicly releasing the suspects image and description will bring up fresh leads in a stale case.

Dabrien Dabe Murphy, the senior solutions architect at Parabon, sits in front of three monitors in a little office on the fourth floor of an unremarkable Reston office building not exactly the first place that comes to mind when you think of a lab. With a few keystrokes, Murphy brings up a revolving 3-D image the back of a head. Another few taps and a face attaches itself along the hairline. The face is a mans: olive skin, greenish eyes, full lips.

Murphy has fed DNA markers, linked to certain facial attributes, into 3-D imaging software to create what he calls a composition. It produces a somewhat distorted image where the face meets the rest of the 3-D model.

Theres a little bit of, okay, manual manipulation to make this not look quite so Frankensteined, Murphy explains. Using his cursor to adjust points and axes in the imaging software, Murphy smooths out the hairline and jaw where the projected face attaches itself to the head.

According to the markers Murphy feeds into the imaging software, the man on the screen is of Northwest African ancestry, with hazel or green eyes; black or brown hair; and few or no freckles. This mans DNA was publicly available, so theyre using it to test their model; they know, from the data included with the DNA, that he is Algerian. The trait predictions come with varying levels of confidence; Parabons scientists are 73.4 percent sure that their skin color prediction is accurate, but they are 94.7 percent confident in the subjects eye color.

All this from 9.6 nanograms of DNA. Thats less than 0.00000001 grams, an amount so small, its hard to compare to anything else.

Snapshot combs through a genotype, searching for significant markers and clusters that might indicate physical attributes and removing unimportant variables.

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New technology generates photo illustration from a persons DNA

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Human DNA gives mice bigger brains

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Injecting mouse embryos with a human DNA sequence leads to a marked increase in brain size -- and may provide insights into Alzheimer's.

Mouse embryo injected with HARE5. Gene actvity is stained blue. Duke University/Silver Lab

The human genetic code is very similar to the genetic code of our closest living relative -- the chimpanzee -- sharing around 95 percent. Of all the differences, however, one is particularly interesting: the human brain is a lot bigger than the brain of a chimp. The brain of a chimp weighs, on average, 384 grams, whereas a human brain is more than triple that, at 1,352 grams.

Although it's not brain size alone that accounts for human intelligence, it certainly plays a pretty important role -- and now, researchers at Duke University have identified the DNA sequence that may be responsible for that particular evolutionary deviation.

How? By using mouse embryos.

The DNA sequence, called HARE5, is a gene activity regulator shown to markedly increase the size of a mouse embryo's brain when injected into the embryo. Compared to a mouse embryo injected with chimpanzee HARE5, the mouse embryo's brain grew 12 percent larger.

"I think we've just scratched the surface, in terms of what we can gain from this sort of study," said Debra Silver, an assistant professor of molecular genetics and microbiology in the Duke University Medical School. "There are some other really compelling candidates that we found that may also lead us to a better understanding of the uniqueness of the human brain."

HARE5 is what is known as an "enhancer", belonging to a group called "human-accelerated regulatory enhancers", including HARE1 through to HARE6. Enhancers are short pieces of DNA inside every genome that control the activity of genes.

To locate the DNA that might influence brain development, the team screened databases of genomic data from humans and chimps, looking for enhancers expressed primarily in the brain tissue early in development, but that also differed between the two species. Of the 106 candidates, the HARE group were near to genes believed to be involved in brain development.

HARE5 was the strongest candidate -- it's located chromosomally near Frizzled8, a molecular pathway indicated in brain development and disease. The team also found that Frizzled8 and HARE5 make physical contact in brain tissue.

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Building Tailor-Made DNA Nanotubes Step by Step

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Newswise Researchers at McGill University have developed a new, low-cost method to build DNA nanotubes block by block a breakthrough that could help pave the way for scaffolds made from DNA strands to be used in applications such as optical and electronic devices or smart drug-delivery systems.

Many researchers, including the McGill team, have previously constructed nanotubes using a method that relies on spontaneous assembly of DNA in solution. The new technique, reported today in Nature Chemistry, promises to yield fewer structural flaws than the spontaneous-assembly method. The building-block approach also makes it possible to better control the size and patterns of the DNA structures, the scientists report.

Just like a Tetris game, where we manipulate the game pieces with the aim of creating a horizontal line of several blocks, we can now build long nanotubes block by block, said Amani Hariri, a PhD student in McGills Department of Chemistry and lead author of the study. By using a fluorescence microscope we can further visualize the formation of the tubes at each stage of assembly, as each block is tagged with a fluorescent compound that serves as a beacon. We can then count the number of blocks incorporated in each tube as it is constructed.

This new technique was made possible by the development in recent years of single-molecule microscopy, which enables scientists to peer into the nano-world by turning the fluorescence of individual molecules on and off. (That groundbreaking work won three U.S.- and German-based scientists the 2014 Nobel Prize in Chemistry.)

Hariris research is jointly supervised by chemistry professors Gonzalo Cosa and Hanadi Sleiman, who co-authored the new study. Cosas research group specializes in single-molecule fluorescence techniques, while Sleimans uses DNA chemistry to design new materials for drug delivery and diagnostic tools.

The custom-built assembly technique developed through this collaboration gives us the ability to monitor the nanotubes as were building them, and see their structure, robustness and morphology, Cosa said.

We wanted to control the nanotubes lengths and features one-by-one, said Sleiman, who holds the Canada Research Chair in DNA Nanoscience. The resulting designer nanotubes, she adds, promise to be far cheaper to produce on a large scale than those created with so-called DNA origami, another innovative technique for using DNA as a nanoscale construction material.

Funding for the research was provided by the Natural Sciences and Engineering Research Council of Canada, the Canada Foundation for Innovation, NanoQubec, the Canadian Institutes of Health Research and the Fonds de recherch du Qubec Nature et technologies. ----------------------------------------------------------------------------

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Carnivorous plant packs big wonders into tiny genome

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Great, wonderful, wacky things can come in small genomic packages.

That's one lesson to be learned from the carnivorous bladderwort, a plant whose tiny genome turns out to be a jewel box full of evolutionary treasures.

Called Utricularia gibba by scientists, the bladderwort is a marvel of nature. It lives in an aquatic environment. It has no recognizable roots. It boasts floating, thread-like branches, along with miniature traps that use vacuum pressure to capture prey.

A new study in the scientific journal Molecular Biology and Evolution breaks down the plant's genetic makeup, and finds a fascinating story.

According to the research, the bladderwort houses more genes than several well-known plant species, such as grape, coffee or papaya -- despite having a much smaller genome.

This incredibly compact architecture results from a history of "rampant" DNA deletion in which the plant added and then eliminated genetic material at a very fast pace, says University at Buffalo Professor of Biological Sciences Victor Albert, who led the study.

"The story is that we can see that throughout its history, the bladderwort has habitually gained and shed oodles of DNA," he says.

"With a shrunken genome," he adds, "we might expect to see what I would call a minimal DNA complement: a plant that has relatively few genes -- only the ones needed to make a simple plant. But that's not what we see."

A unique and elaborate genetic architecture

In contrast to the minimalist plant theory, Albert and his colleagues found that U. gibba has more genes than some plants with larger genomes, including grape, as already noted, and Arabidopsis, a commonly studied flower.

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'DNA spellchecker' means that genes aren't all equally likely to mutate

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A study that examined 17 million mutations in the genomes of 650 cancer patients concludes that large differences in mutation rates across the human genome are caused by the DNA repair machinery.

'DNA spellchecker' is preferentially directed towards more important parts of chromosomes that contain key genes.

The study illustrates how data from medical sequencing projects can answer basic questions about how cells work.

The work, performed by two scientists from the EMBL-CRG Systems Biology Unit in Barcelona, will be published online in Nature on 23rd February. Copying the large book that it is our genome without mistakes every time a cell divides is a difficult job. Luckily, our cells are well-equipped to proof-read and repair DNA mistakes. Now, two scientists at the Centre for Genomic Regulation in Barcelona have published a study showing that mistakes in different parts of our genome are not equally well corrected. This means that some of our genes are more likely to mutate and so contribute to disease than others.

The scientists analysed 17 million 'single nucleotide variants' -- mutations in just one nucleotide (letter) of the DNA sequence -- by examining 650 human tumours from different tissues. These were 'somatic' mutations, meaning they are not inherited from parents or passed down to children, but accumulate in our bodies as we age. Such somatic mutations are the main cause of cancer. Many result from mutagens, such as tobacco smoke or ultraviolet radiation, and others come from naturally occurring mistakes in copying DNA as our tissues renew.

Ben Lehner and his team had previously described that somatic mutations are much more likely in some parts of the human genome, thus damaging genes that may cause cancer. In a new paper published on 23rd February in Nature, they show that this is because genetic mistakes are better repaired in some parts of the genome than in others. This variation was generated by a particular DNA repair mechanism called "mismatch repair" -- a sort of a spellchecker that helps fix the errors in the genome after copying. Lehner and Supek show that the efficiency of this 'DNA spellchecker' varies depending on the region of the genome, with some parts of chromosomes getting more attention than others.

Turning the tables on mutation rates

The work presented by Lehner and Supek sheds new light on a process that was unexplored -- what makes some parts of the human genome more vulnerable to damage? "We found that regions with genes switched on had lower mutation rates. This is not because less mistakes are happening in these regions but because the mechanism to repair them is more efficient," explains Ben Lehner, group leader, ICREA and AXA professor of risk prediction in age-related diseases at the EMBL-CRG Systems Biology unit in Barcelona. The 'mismatch repair' cellular machinery is extremely accurate when copying important regions containing genes that are key for cell functioning, but becomes more relaxed when copying less important parts. In other words, there appears to be a limited capacity for DNA repair in our cells, which is directed where it matters most.

The CRG researchers also found that the rate of mutation differs for around 10% of the human genome in cells originating from different tissues. In particular, liver, colorectal and lymphocyte malignancies present more mutations in some parts of our chromosomes, while breast, ovarian and lung cancers accumulate more mutations in other places. They found that genes that are important and switched on (expressed) in a particular tissue also exhibit less mutations in tumours of that tissue; the effect extends into the surrounding DNA. But what gives the important genes a higher resilience to damage?

"The difference is not in the number of new mutations but in the mechanism that keeps these mutations under control," comments Fran Supek, CRG postdoctoral researcher and first author of the paper. "By studying cancer cells, we now know more about maintaining DNA integrity, which is really important for healthy cells as well," he adds. Once the 'genomic spellchecker' has been disabled in a cell, the scientists observed that genetic information started decaying not only very rapidly, but also equally in all parts of the genome -- neither the important nor the less important parts can were repaired well anymore. DNA mismatch repair is known to be switched off in some tumours from the colon, stomach and uterus, producing 'hypermutator' cancer in those organs.

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From the first human genome, to a great library of life

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Geneticist Eric S. Lander, one of the principal leaders of the Human Genome Project that mapped the entire human genome in 2003, offered a rare glimpse into the genetic library of life being created by a global community of scientists. This veritable catalogue has already begun to help decode the genetic basis of certain cancers, heart disease and schizophrenia.

A packed audience of students, scientists and medical practitioners heard Prof Lander speak on The Human Genome and Beyond: A 35 year Journey of Genomic Medicine at the fifth edition of the Cell Press-TNQ Distinguished Lectureship Series at the All India Institute of Medical Sciences here on Monday.

Over the last decade, genetic research has been revolutionised and the costs of genome sequencing have dropped drastically. While mapping a single human genome (as part of the Human Genome Project 1990-2003) costs $3 billion, today it costs less than $ 3,000.

This breakthrough opens up enormous opportunities to understand diseases, he said. Today, for instance, over 108 genes can be associated with schizophrenia, and particular genetic mutations can be linked to heart attacks early in life.

And yet, we have only scratched the surface, Prof Lander said. Discoveries require studying huge samples for every major disease. And for that our healthcare systems have to turn into learning systems.

The Global Alliance for Genomics and Health comprising 246 organisations in 28 countries -- including India -- is one such endeavour to create a critical mass of data.

It is imperative, however that the data remains shareable, said Prof Lander, who is the Founding Director of the Broad Institute (linking MIT, Harvard University and hospitals).

But genetic data must belong to patients, who have the right to share it with their privacy protected.

India, with the extraordinary size of its population is, from the genetic point of view, the single most interesting population in the world.

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From the first human genome, to a great library of life

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