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Category Archives: Transhuman News

Education is Important :: SOLO 105 Kill Double DNA on Solar – Video

Posted: January 31, 2015 at 4:44 am


Education is Important :: SOLO 105 Kill Double DNA on Solar
Twitter: https://twitter.com/TheFatZeus Watch me on Twitch: http://www.twitch.tv/thefatzeus Clan:https://www.youtube.com/channel/UCqWm5skrdP63vvPdsk9Lzlg Intro Song: https://www.youtube...

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Education is Important :: SOLO 105 Kill Double DNA on Solar - Video

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Call of Duty: Advanced Warfare DNA – Video

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Call of Duty: Advanced Warfare DNA
Call of Duty: Advanced Warfare https://store.sonyentertainmentnetwork.com/#!/tid=CUSA00803_00.

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Advanced Warfare HILARIOUS Killcams – 360 No Scope, Insane DNA Bomb and MORE! – Video

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Advanced Warfare HILARIOUS Killcams - 360 No Scope, Insane DNA Bomb and MORE!
Ahrora returns with some hilarious Call of Duty Killcams! These reactions just keep getting better! Smack the HELL out of that Like button to show your support! DIRECTOR #39;S CHANNEL: http://www.yout.

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Advanced Warfare HILARIOUS Killcams - 360 No Scope, Insane DNA Bomb and MORE! - Video

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DNA – Esoteric Online

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Deoxyribonucleic acid (DNA) is a nucleic acid that contains the genetic instructions used in the development and functioning of all known living organisms

The essence of evolution can also be found in religion, and therefore in the realm of the evolution of consciousness... in the book "Hermetic Code in DNA: The Sacred Principles in the Ordering of the Universe" writer Michael Hayes made an examination of the precise code that connects ancient spirituality with modern science. It: Shows how the numerical patterns in ancient philosophies are evident in both the structure of the universe and the helical structure of DNA Reveals that music theory comes from an intuitive understanding of the resonant harmony of the cosmos

Many have observed the distinct numerical patterns embedded in ancient philosophies and religions from all over the world; others have noted that these same patterns are apparent in many of the theories of groundbreaking science. Michael Hayes reveals that there is a precise code, the Hermetic Code, that connects these patterns--information once known to ancient cultures but apparently lost over time. Mirrored in the structure of this code are the ordering principles of the universe and, intriguingly, also the harmonic ratios of music. Our notions of what is harmonious in music may therefore arise not from an abstract aesthetic sense but as a response to an intuition of a fundamental cosmic harmony.

The resonance between biology and cosmology shows that life is music, complete with overtones--nowhere more strikingly present than in the helical structure of life itself: DNA.

Everything in the universe vibrates and oscillates. Therefore the connecting link between all forms of energy is vibration, sympathetic harmony, and resonance. Dr. Dan Burisch, David Wilcock, and others have discovered that a simply quartz crystal, electricity, and water are all the ingredients needed to create a medium for spontaneous DNA to appear in the vacuum..

Every mind effects the other.. and our unification creates this reality around us. However, we are not the only intelligent consciousness in this universe. Our planet Earth, the sun, and all of it's sister stars are very much alive and consciouses.. And they evolve on a macro scale just like the amoeba evolve on a micro scale. 2012 is believed to mark the evolution of our world... The spectral rapture in which our DNA will unravel and unify human beings who are bound by an ancient cosmic prophecy.

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DNA Leads To Arrest In Cold Rape Case

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NORWICH DNA led police to a man who they say beat and raped a woman in an alley more than five years ago.

Alexander S. Perry, 24, of Central Avenue was arrested on a warrant Thursday charging him with first-degree sexual assault, second-degree assault, first-degree threatening and first-degree unlawful restraint, police said.

He was in custody on $500,000 bail Friday morning and was scheduled to be arraigned in Superior Court in Norwich later in the day, they said.

According to police, on April 29, 2009, officers responded to a report of a sexual assault that happened in an alley behind a business on Central Avenue. A woman told them she had been walking in the area when a man she didn't know called over to her.

She walked toward him and he grabbed her, beat her and sexually assaulted her, police said.

The woman had what police described as "moderate" injuries, including broken bones in her face.

An extensive search by officers and a scent-sniffing dog failed to lead police to a suspect, police said. Evidence, including the suspect's DNA, was taken from the scene and, over the years, occasionally compared to DNA profiles that are stored in state and national databases, they said.

On Jan. 12, police learned that during one of those comparisons, staff at the state forensic lab found a match.

On Thursday, Community Police Officer Ken Wright saw the suspect now identified as Perry walking on Central Avenue, the same street where the rape happened, police said.

Wright arrested him.

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DNA nanoswitches reveal how life's molecules connect

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A complex interplay of molecular components governs almost all aspects of biological sciences -- healthy organism development, disease progression, and drug efficacy are all dependent on the way life's molecules interact in the body. Understanding these bio-molecular interactions is critical for the discovery of new, more effective therapeutics and diagnostics to treat cancer and other diseases, but currently requires scientists to have access to expensive and elaborate laboratory equipment.

Now, a new approach developed by researchers at the Wyss Institute for Biologically Inspired Engineering, Boston Children's Hospital and Harvard Medical School promises a much faster and more affordable way to examine bio-molecular behavior, opening the door for scientists in virtually any laboratory world-wide to join the quest for creating better drugs. The findings are published in February's issue of Nature Methods.

"Bio-molecular interaction analysis, a cornerstone of biomedical research, is traditionally accomplished using equipment that can cost hundreds of thousands of dollars," said Wyss Associate Faculty member Wesley P. Wong, Ph.D., senior author of study. "Rather than develop a new instrument, we've created a nanoscale tool made from strands of DNA that can detect and report how molecules behave, enabling biological measurements to be made by almost anyone, using only common and inexpensive laboratory reagents."

Wong, who is also Assistant Professor at Harvard Medical School in the Departments of Biological Chemistry & Molecular Pharmacology and Pediatrics and Investigator at the Program in Cellular and Molecular Medicine at Boston Children's Hospital, calls the new tools DNA "nanoswitches."

Nanoswitches comprise strands of DNA onto which molecules of interest can be strategically attached at various locations along the strand. Interactions between these molecules, like the successful binding of a drug compound with its intended target, such as a protein receptor on a cancer cell, cause the shape of the DNA strand to change from an open and linear shape to a closed loop. Wong and his team can easily separate and measure the ratio of open DNA nanoswitches vs. their closed counterparts through gel electrophoresis, a simple lab procedure already in use in most laboratories, that uses electrical currents to push DNA strands through small pores in a gel, sorting them based on their shape

"Our DNA nanoswitches dramatically lower barriers to making traditionally complex measurements," said co-first author Ken Halvorsen, formerly of the Wyss Institute and currently a scientist at the RNA Institute at University of Albany. "All of these supplies are commonly available and the experiments can be performed for pennies per sample, which is a staggering comparison to the cost of conventional equipment used to test bio-molecular interactions."

To encourage adoption of this method, Wong and his team are offering free materials to colleagues who would like to try using their DNA nanoswitches.

"We've not only created starter kits but have outlined a step-by-step protocol to allow others to immediately implement this method for research in their own labs, or classrooms" said co-first author Mounir Koussa, a Ph.D. candidate in neurobiology at Harvard Medical School.

"Wesley and his team are committed to making an impact on the way bio-molecular research is done at a fundamental level, as is evidenced by their efforts to make this technology accessible to labs everywhere," said Wyss Institute Founding Director Donald Ingber, M.D., Ph.D., who is also the Judah Folkman Professor of Vascular Biology at Boston Children's Hospital and Harvard Medical School and a Professor of Bioengineering at Harvard SEAS. "Biomedical researchers all over the world can start using this new method right away to investigate how biological compounds interact with their targets, using commonly-available supplies at very low cost."

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Hatsune Miku – Daidai Genome cover – Video

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Hatsune Miku - Daidai Genome cover

By: Kanna Ohime

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genome defi boost working check – Video

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genome defi boost working check
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New software analyzes human genomes faster than other available technologies

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Investigators at Nationwide Children's Hospital have developed an analysis "pipeline" that slashes the time it takes to search a person's genome for disease-causing variations from weeks to hours. An article describing the ultra-fast, highly scalable software was published in the latest issue of Genome Biology.

"It took around 13 years and $3 billion to sequence the first human genome," says Peter White, PhD, principal investigator and director of the Biomedical Genomics Core at Nationwide Children's and the study's senior author. "Now, even the smallest research groups can complete genomic sequencing in a matter of days. However, once you've generated all that data, that's the point where many groups hit a wall. After a genome is sequenced, scientists are left with billions of data points to analyze before any truly useful information can be gleaned for use in research and clinical settings."

To overcome the challenges of analyzing that large amount of data, Dr. White and his team developed a computational pipeline called "Churchill." By using novel computational techniques, Churchill allows efficient analysis of a whole genome sample in as little as 90 minutes.

"Churchill fully automates the analytical process required to take raw sequence data through a series of complex and computationally intensive processes, ultimately producing a list of genetic variants ready for clinical interpretation and tertiary analysis," Dr. White explains. "Each step in the process was optimized to significantly reduce analysis time, without sacrificing data integrity, resulting in an analysis method that is 100 percent reproducible."

The output of Churchill was validated using National Institute of Standards and Technology (NIST) benchmarks. In comparison with other computational pipelines, Churchill was shown to have the highest sensitivity at 99.7 percent; highest accuracy at 99.99 percent and the highest overall diagnostic effectiveness at 99.66 percent.

"At Nationwide Children's we have a strategic goal to introduce genomic medicine into multiple domains of pediatric research and healthcare. Rapid diagnosis of monogenic disease can be critical in newborns, so our initial focus was to create an analysis pipeline that was extremely fast, but didn't sacrifice clinical diagnostic standards of reproducibility and accuracy" says Dr. White. "Having achieved that, we discovered that a secondary benefit of Churchill was that it could be adapted for population scale genomic analysis."

By examining the computational resource use during the data analysis process, Dr. White's team was able to demonstrate that Churchill was both highly efficient (>90 percent resource utilization) and scaled very effectively across many servers. Alternative approaches limit analysis to a single server and have resource utilization as low as 30 percent. This efficiency and capability to scale enables population-scale genomic analysis to be performed.

To demonstrate Churchill's capability to perform population scale analysis, Dr. White and his team received an award from Amazon Web Services (AWS) in Education Research Grants program that enabled them to successfully analyze phase 1 of the raw data generated by the 1000 Genomes Project -- an international collaboration to produce an extensive public catalog of human genetic variation, representing multiple populations from around the globe. Using cloud-computing resources from AWS, Churchill was able to complete analysis of 1,088 whole genome samples in seven days and identified millions of new genetics variants.

"Given that several population-scale genomic studies are underway, we believe that Churchill may be an optimal approach to tackle the data analysis challenges these studies are presenting," says Dr. White.

The Churchill algorithm was licensed to Columbus-based GenomeNext LLC, which has built upon the Churchill technology to develop a secure and automated software-as-a-service platform that enables users to simply upload raw whole-genome, exome or targeted panel sequence data to the GenomeNext system and run an analysis that not only identifies genetic variants but also generates fully annotated datasets enabling filtering and identification of pathogenic variants. The company provides genomic data analysis solutions that simplify the process of data management and automate analysis of large scale genomic studies. The system was also developed with the research and clinical market in mind, offering a standardized pipeline that is well suited to settings where customers have to meet regulatory requirements.

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New Software Analyzes Human Genomes Faster than Other Available Technologies, Empowering Population Scale Genomic …

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Newswise Investigators at Nationwide Childrens Hospital have developed an analysis pipeline that slashes the time it takes to search a persons genome for disease-causing variations from weeks to hours. An article describing the ultra-fast, highly scalable software was published in the latest issue of Genome Biology (http://genomebiology.com/2015/16/1/6/abstract).

It took around 13 years and $3 billion to sequence the first human genome, says Peter White, PhD, principal investigator and director of the Biomedical Genomics Core at Nationwide Childrens and the studys senior author. Now, even the smallest research groups can complete genomic sequencing in a matter of days. However, once youve generated all that data, thats the point where many groups hit a wall. After a genome is sequenced, scientists are left with billions of data points to analyze before any truly useful information can be gleaned for use in research and clinical settings.

To overcome the challenges of analyzing that large amount of data, Dr. White and his team developed a computational pipeline called Churchill. By using novel computational techniques, Churchill allows efficient analysis of a whole genome sample in as little as 90 minutes.

Churchill fully automates the analytical process required to take raw sequence data through a series of complex and computationally intensive processes, ultimately producing a list of genetic variants ready for clinical interpretation and tertiary analysis, Dr. White explains. Each step in the process was optimized to significantly reduce analysis time, without sacrificing data integrity, resulting in an analysis method that is 100 percent reproducible.

The output of Churchill was validated using National Institute of Standards and Technology (NIST) benchmarks. In comparison with other computational pipelines, Churchill was shown to have the highest sensitivity at 99.7 percent; highest accuracy at 99.99 percent and the highest overall diagnostic effectiveness at 99.66 percent.

At Nationwide Childrens we have a strategic goal to introduce genomic medicine into multiple domains of pediatric research and healthcare. Rapid diagnosis of monogenic disease can be critical in newborns, so our initial focus was to create an analysis pipeline that was extremely fast, but didnt sacrifice clinical diagnostic standards of reproducibility and accuracy says Dr. White. Having achieved that, we discovered that a secondary benefit of Churchill was that it could be adapted for population scale genomic analysis.

By examining the computational resource use during the data analysis process, Dr. Whites team was able to demonstrate that Churchill was both highly efficient (>90 percent resource utilization) and scaled very effectively across many servers. Alternative approaches limit analysis to a single server and have resource utilization as low as 30 percent. This efficiency and capability to scale enables population-scale genomic analysis to be performed.

To demonstrate Churchills capability to perform population scale analysis, Dr. White and his team received an award from Amazon Web Services (AWS) in Education Research Grants program that enabled them to successfully analyze phase 1 of the raw data generated by the 1000 Genomes Project an international collaboration to produce an extensive public catalog of human genetic variation, representing multiple populations from around the globe. Using cloud-computing resources from AWS, Churchill was able to complete analysis of 1,088 whole genome samples in seven days and identified millions of new genetics variants.

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