Monthly Archives: January 2014

DROID DNA Camera Sample916 – Video

Posted: January 18, 2014 at 7:43 am


DROID DNA Camera Sample916

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DNA clamps could stop cancer in its tracks

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Scientists have developed a special DNA clamp to act as a diagnostic nano machine. It's capable of detecting genetic mutations responsible for causing cancers, hemophilia, sickle cell anemia and other diseases, more efficiently than existing techniques. Not only can the clamp be used to develop more advanced screening tests, but it could also help create more efficient DNA-based nano machines for targeted drug delivery.

To catch diseases at their earliest stages, researchers have begun looking into creating quick screening tests for specific genetic mutations that pose the greatest risk of developing into life-threatening illnesses. When the nucleotide sequence that makes up a DNA strand is altered, it is understood to be a mutation; specific types of cancers are understood to be caused by certain mutations. Even if one single nucelotide base has been inserted, deleted or changed, it can change the entire DNA sequence scientists call this a single point mutation.

To detect this type of mutation and others, researchers typically use molecular beacons or probes, which are DNA sequences that become fluorescent on detecting mutations in DNA strands. The team of international researchers that developed the DNA clamp state that their diagnostic nano machine allows them to more accurately differentiate between mutant and non-mutant DNA.

"Our DNA clamp probes can perform very similar applications compared to molecular beacons, which are being used in many diagnostic clinics around the world since they enable the rapid, fluorescent detection of specific DNA sequences, or mutations," Alexis Valle-Blisle, a Chemistry Professor at the Universit de Montral, Canada tells Gizmag."However, since they bind DNA using a clamp mechanism, i.e. a single DNA sequence from a patient is recognized by two DNA sequences on our clamp, they are now able to detect single point mutations with much more efficiency than molecular beacons do."

According to the team, the DNA clamp is designed to recognize complementary DNA target sequences like a clamp-switch. As soon as it recognizes them, it binds with them to form a stable triple helix structure, while fluorescing at the same time. Being able to identify single point mutations more easily this way is expected to help doctors identify different types of cancer risks, with greater sensitivity, accuracy and precision, and to inform patients about the specific cancers they are likely to develop. Diagnosing cancer at a genetic level could potentially help arrest the disease, before it even develops properly.

"Cancer is a very complex disease that is caused by many factors," explains Valle-Blisle. "However, most of these factors are written in DNA. We only envisage identifying the cancers or potential of cancer. As our understanding of the effect of mutations in various cancer will progress, early diagnosis of many forms of cancer will become more and more possible."

Currently the team has only tested the probe on artificial DNA, and plans are in the works to undertake testing on human samples. The team believes that the DNA clamp will "provide a new weapon in the toolbox of nano engineers, to help them to design more efficient and versatile DNA nano machines." For instance, to deliver drugs to only the tumor cells, and not healthy cells, scientists can make use of DNA-based nano machines, that are created by assembling many different small DNA sequences together to create a 3D structure, kind of like a box. When it encounters a disease marker, the box opens up and delivers the drug, enabling smart drug delivery. The DNA clamps are expected to help this whole process function better.

"The clamp switches that we have designed and optimized can recognize a DNA sequence with high precision and high affinity," Professor Francesco Ricci, at the University of Rome,Tor Vergata, Italy, tells us."This means that our clamp switches can be used, for example, as super-glue to assemble these nano machines and create a better and more precise 3D structure that can, for example, open in the presence of a disease marker and release a drug."

The international research project was funded by the US National Institutes of Health, the Italian Ministry of Universities and Research (MIUR), the Natural Sciences and Engineering Research Council of Canada, the Bill & Melinda Gates Foundation Grand Challenges Explorations program and the European Commission Marie Curie Actions program. Their paper describing the development was recently published in the journal ACS Nano.

Source: Universit de Montral

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Largest Genome Ever Sequenced Belongs To Locust Species

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January 17, 2014

April Flowers for redOrbit.com Your Universe Online

The whole genome sequence of Locust (Locusta migratoria), the most widespread locust species, has been successfully decoded by researchers from the Institute of Zoology, Chinese Academy of Sciences, BGI and other institutes. The researchers were surprised by the remarkably large (6.5 gigabytes) yielded genome, which is the largest animal genome sequenced so far.

Researchers have been surprised to find that a single locust is able to eat its own body-weight in food in a single day. Proportionately, this amount is 60 times a humans daily consumption. Locusts are capable of inflicting famine and wiping out livelihoods during swarms, which can cost countries billions of dollars in lost harvests and eradication efforts.

For the current study, published in Nature Communications, the research team used next generation sequencing technology to sequence L. migratoria. This technology yielded 721Gb of data, covering 114 x of the 6.3Gb locust genome size. The team was able to annotate and predict about 17,307 gene models and identify over 2,639 repeat gene families. The team also discovered that the top ten repeat families only represented 10 percent of the total genome sequences. This suggests that there were no dominant families in the L. migratoria genome.

The research team found that the reason why the locust has such a large genome compared to other reference insect genomes is a transportable element proliferation combined with slow rates of loss for these elements. Statistics reveal that repetitive elements constituted 60 percent of the assembled genome. The team also found that the genome exhibited the lowest rate of DNA deletions relative to the other insects.

The researchers performed comparative methylome and transcriptome analysis to investigate the potential involvement of epigenetic regulation in locust phase change. Interestingly, the researchers found that repetitive elements were highly methylated and introns had higher methylation levels than exons in the locust genome. They also found that there had been changes in genes involved in the regulation of the cytoskeletal microtubular system, as well as in neuronal activity during the onset of phase change in locusts from solitarious to swarm.

The most distinguishing feature of a locust is the long distance flight, which enables it to fly at speeds of up to hundreds of kilometers an hour; it is even able to cross the ocean. The current researchers found that the locust had developed a highly efficient energy supply system. This was accomplished by the expansion of genes in lipid metabolism and detoxification to fulfill the intensive energy consumption during its long-distance flight. The locust also displays an expansion of its gustatory and olfactory receptor gene families which are for its strong adaptation to host plant recognition.

In order to develop more effective insecticides, the research team identified the gene targets for pest control and new insecticides, such as cys-loop ligand-gated ion channels and G-protein-coupled receptors. These are considered to be major traditional insecticide targets, and the repertoire of several biological processes that could serve as mechanistic targets and lead to the development of specific and sustainable pest control methods.

Source: April Flowers for redOrbit.com - Your Universe Online

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Largest Genome Ever Sequenced Belongs To Locust Species

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World’s largest animal genome belongs to locust: New insight explains swarming, long-distance migratory behaviors

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Jan. 16, 2014 Researchers from Institute of Zoology, Chinese Academy of Sciences, BGI and other institutes have successfully decoded the whole genome sequence of Locust (Locusta migratoria), the most widespread locust species. The yielded genome is remarkably big- at 6.5 gigabytes, which is the largest animal genome sequenced so far. The latest study has been published online in the journal Nature Communications.

One surprise from the study is that a single locust can eat its own bodyweight in food in a single day; this is, proportionately, 60 times a human's daily consumption. They are capable of inflicting famine and wiping out livelihoods when they swarms, which can cost countries billions of dollars in lost harvests and eradication efforts.

In this study, researchers sequenced Locusta migratoria using next-gen sequencing technology, totally yielding 721Gb of data, which covered 114 of the 6.3Gb locust genome size. They annotated and predicted about 17,307 gene models, and identified over 2,639 repeat gene families. Moreover, they discovered that the top ten repeat families only represented 10% of the total genome sequences, suggesting that there were no dominant families in the L. migratoria genome.

Compared with other reference insect genomes, researchers found the reason why locust has such large genome is transposable element proliferation combined with slow rates of loss for these elements. According to statistics, repetitive elements constituted 60% of the assembled genome. The transposable element in the Locust genome was expanded when comparing with the other insects. Besides, they also found that the locust genome exhibited the lowest rate of DNA deletions relative to the other insects.

To investigate the potential involvement of epigenetic regulation in locust phase change, researchers performed comparative methylome and transcriptome analysis. One interesting finding was that repetitive elements were highly methylated and introns had higher methylation levels than exons in locust genome. It was also noteworthy that there had changes in genes involved in the regulation of the cytoskeletal microtubular system and in neuronal activity during the onset of phase change in locusts from solitarious to swarm.

As we all know, locust has an most distinguishing feature- the long-distance flight- which enables them can fly at speed of hundreds of kilometers an hour, or even cross the ocean. In this study, researchers found that locust had developed a highly efficient energy supply system by expansion genes in lipid metabolism and detoxification to fulfill the intensive energy consumption during their long-distance flight. The expansion of its gustatory and olfactory receptor gene families is for its strong adaptation to host plant recognition.

To advance the development of new effective insecticides, researchers identified the gene targets for pest control and new insecticides, such as cys-loop ligand-gated ion channels and G-protein-coupled receptors, which are considered to be major traditional insecticide targets, and the repertoire of several biological processes that may serve as mechanistic targets and lead to the development of specific and sustainable pest control methods.

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World's largest animal genome belongs to locust: New insight explains swarming, long-distance migratory behaviors

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Same cell death pathway involved in three forms of blindness, study finds

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Jan. 16, 2014 Gene therapies developed by University of Pennsylvania School of Veterinary Medicine researchers have worked to correct different forms of blindness. While effective, the downside to these approaches to vision rescue is that each disease requires its own form of gene therapy to correct the particular genetic mutation involved, a time consuming and complex process.

Hoping to develop a treatment that works more broadly across diseases, a Penn Vet team used canine disease models to closely examine how retinal gene activity varied during the progression of three different forms of inherited vision disease. Their results turned up an unexpected commonality: Early on in each of the diseases, genes involved in the same specific pathway of cell death appeared to be activated. These findings point to possible interventions that could curb vision loss across a variety of inherited retinal diseases.

The work, published in PLOS ONE, was conducted by Sem Genini, a senior research investigator; William A. Beltran, assistant professor of ophthalmology; and Gustavo D. Aguirre, professor of medical genetics and ophthalmology, all of Penn Vet's Department of Clinical Studies, Philadelphia.

The team examined three forms of retinal degenerative diseases, rod cone dysplasia 1 being the most severe, or earliest onset, followed by X-linked progressive retinal atrophy 2 and then early retinal degeneration. All of these diseases involve the death of photoreceptor cells and each is caused by a distinct genetic mutation. But what scientists did not know is how the mutations trigger a molecular signaling pathway that leads to the death of photoreceptor cells.

"What we have in mind is to be able to address multiple forms of disease with one treatment," Beltran said. "We wanted to get a better understanding of whether there are any common cell death or cell survival pathways that could be targeted in some of these diseases."

The researchers looked at the activity of 112 genes in diseased retinas and compared it to gene activity in normal retinas. They assessed gene activity at time points known to correspond with key phases of disease: the "induction phase," the time before the peak level of photoreceptor cell death; the "execution phase," when the highest rates of photoreceptor cell death occur; and the "chronic phase," during which photoreceptor cell death continues at somewhat reduced levels.

During the execution and chronic phases of disease, the researchers identified a number of genes involved in programmed cell death, or apoptosis, that had noticeably different patterns of expression between the diseased and normal dogs.

Of note, several proteins involved in the tumor necrosis factor, or TNF, pathway increased in activity during the induction and execution phases. This pathway is implicated in many diseases, from diabetes to cancer to rheumatoid arthritis.

"This is quite a new result," Genini said. "It was not expected to have the TNF pathway upregulated."

"We assumed," Aguirre said, "the diseases would be different from one another and that cells would commit suicide by their own specific pathway and that perhaps quite late they would have a common final pathway. But what this shows is that there is an early trigger that is quite similar among all three diseases."

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New Gene Machine Could Mean More Accurate Diagnosis

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A new supercomputer can sequence 20,000 genomes in a year for $1,000 a piece.

On Tuesday, Illumina, a global company that specializes in genomic analysis, announced the sale of a new genetic sequencing machine, that is faster and more affordable than existing technology.

"The new sequencer packs high-throughput performance into an affordable desktop form factor, enabling researchers to perform the most popular sequencing applications in less than a day,"said Jay Flatley, CEO of Illumina in a press release.

[READ: Researchers Link Aging Gene to Blood Cancer]

The new technology can sequence a whole human genome in a single run. And the sequencing data can be fed through open source or commercial programs or transferred, analyzed and stored in a secure space, the release noted.

The new machine can sequence 20,000 genomes in a year for $1,000 a piece, says HPC Wire. It can process 16 complete human genomes in three days. The "$1000 genome" is a long-sought marker of advancement that industry has seen as "a tipping point in the pace of genetic discovery" says Aaron Kroll at BioITWorld.

Dr. Gianrico Farrugia, director for the Center for Individualized Medicine at the Mayo Clinic, says that the new machinery's reduced cost and its ability to do large-scale processing will affect the reliability of doctor's results. When testing a person's genome having a larger data set to compare anomalies with will allow doctors to rule-out false positives that can sometimes occur when the pool of comparison data is too small. Doctors need to be certain that "what we call as abnormal is in fact abnormal," he says.

"So, being able to do this significantly larger scale sequencing at a lower cost allows you to collect information that you can apply to your individual patient, because you have more information," he adds.

Farrugia says he knew that the technology was being tested, but didn't know when it would be available. He's excited to try out the new machines and apply them to patient care. The first full human genome sequence was published in April 2003 for $3 billion, according to HPC Wire.

[STUDY: Same Genes May Cause Alcohol Abuse, Eating Disorders]

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Man punched Funny Books Book Men Male Humour Present Gift Grumpy Old sh*t my Dad says father’s day – Video

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Man punched Funny Books Book Men Male Humour Present Gift Grumpy Old sh*t my Dad says father #39;s day
PLANET ME: Some Sarcastic Ramblings on Anything and Everything that Amuses or Irritates - me. New Book - out as E-Book and Paperback on AMAZON soon. Politica...

By: Tony Eezisit Eezifestival

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Man punched Funny Books Book Men Male Humour Present Gift Grumpy Old sh*t my Dad says father's day - Video

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Paranormal video codes that destroyed dreams pineal gland secret plot censorship! – Video

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Paranormal video codes that destroyed dreams pineal gland secret plot censorship!
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By: Giosaf Lefodas

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Paranormal video codes that destroyed dreams pineal gland secret plot censorship! - Video

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Dethrone The Sovereign – "Transhuman" Play Through (Guitars, Bass, Keys) – Video

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Dethrone The Sovereign - "Transhuman" Play Through (Guitars, Bass, Keys)
Guitar, bass, and keyboard play through of "Transhuman" off our latest EP "Autocracy Dismantled", available on iTunes and Bandcamp now! Note: The bass is off...

By: Dethrone The Sovereign

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Dethrone The Sovereign - "Transhuman" Play Through (Guitars, Bass, Keys) - Video

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Doctors carry out post-mortem on Sunanda’s body

Posted: at 7:40 am

New Delhi: A three-member team of senior doctors at AIIMS here today began post-mortem on the body of Sunanda Pushkar, wife of Union Minister Shashi Tharoor, even as police continued to probe various angles including suicide in the case.

Hours after his wife was found dead, the 57-year-old Union Minister of State for Human Resources was admitted to AIIMS after complaining of chest pain.

Sudhir Gupta, Head of Forensic Sciences Department at AIIMS said the post-mortem is being videographed to ensure transparency in the procedure.

Pushkar was found dead in her suite at the Leela Palace hotel last evening and the body was shifted to AIIMS at around 3:30 AM for post-mortem.

Tharoor was admitted to the ICU of the cardiothoracic centre of the AIIMS and a number of investigations including ECG were carried out on him. The Minister was discharged at around 12 noon.

Doctors said he was brought to the hospital with a "cardiac condition" but he is stable now.

Continuing investigation, police questioned a number of hotel staff and checked the CCTV footage of the lobby of the third floor of the luxury hotel where she was staying.

Sources in police said call details record as well as Pushkar's tweets were being checked. Pushkar and Tharoor had checked into the hotel on Thursday as their home was being painted.

A number of hotel staff, including those who had gone to her suite, were being questioned to corroborate the version of Tharoor and his staff.

Pushkar and Tharoor were at the centre of a raging controversy when reports emerged that she was upset over reported text and tweet messages between her husband and Mehr Tarar, a Pakistani journalist.

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Doctors carry out post-mortem on Sunanda's body

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