Category Archives: Genome

Watch How To Get Pregnant Immediately - Tips You May Not Know That Can Actually Help You Get
click here to learn more==)) yupurl.com Best ways to get pregnant. Finally a step-by-step plan to get pregnant quickly and stop wasting time! notgettingpregnantreasons. How To Get Pregnant - Part I By Dr.Polaneczky Procreation is like Windows Explorer -- it #39;s built into the operating system. gettingpregnanttips. gettingpregnant. The Physics Classroom Tutorial. A set of instructional pages written in an easy-to-understand language and complemented by graphics and Check Your Understanding sections. Center for Human Reproduction is a world renowned IVF, infertility, fertility, egg donation and gender selection center in New York, NY. AED Pregnancy Registry; Additional Resources; Research eNewsletter; The only way to cure epilepsy is through research and new discoveries. Miten asennan palovaroittimen? Toimiva palovaroitin haistelee ilmaa jatkuvasti ja havaitsee savun nopeasti, kunhan varoitin on oikein asennettu. Welcome To Fertility Centers Of New England If you are having difficulty conceiving, you #39;ve come to the right place. From conception and throughout your life, your genome is in control. fertility.From:fatfatloseViews:0 0ratingsTime:00:59More inEntertainment

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Watch How To Get Pregnant Immediately - Tips You May Not Know That Can Actually Help You Get - Video

Virus-Structure, Genetics,Culture and Diseases....
Virus: Structure, Genetics, Culture and Diseases: Viruses are infectious agents. They are much smaller than the bacteria. Their approximate size ranges from 20 to 300 nm. Viruses are incapable of independent growth in artificial media. They can grow only in animal or plant cells or in microorganisms. Hence they are referred to as obligate intracellular parasites. They reproduce in these cells by replication. Replication is a process in which many copies or replicas of the viral component are assembled and made to represent the progeny. They lack metabolic machinery of their own to generate energy or to synthesize proteins. They depend on the host cells to carry out these vital functions. The bacterial viruses are called bacteriophages. These viruses infect the bacteria and multiply inside the bacterial body and cause the lysis of bacteria (lytic cycle) or integrate themselves with the bacterial genome (lysogeny). http://www.edufine.netFrom:eASYtIPS4YOUViews:0 0ratingsTime:01:37More inEducation

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Virus-Structure, Genetics,Culture and Diseases.... - Video

Watch Behind The Scenes: Ted Williams Records Kraft Macaroni Cheese Commercial - Making Of Ted
Watch full movie here : snipurl.com TED self-replicating species diffusion of innovation inspiring organizations creative breakthroughs Predictably Irrational how to be inspiring Michael Pritchard irrational behavior physical attraction warwick university water purification synthetic genomics Bluewater+Shopping Watch is economics World of Warcraft inspiring leaders decision making inspire action synthetic life tedxkids@Brussels who is inspiring tedxwarwick 2011 inspiring action inspiring people good advertising optical illusion visual illusions natural disaster cheap technology entrepreneurship project plateau time management Wright brothers consumer choice disaster relief genome sequence tedtalks Craig Venter incrementalists decision-making Gamification making choices cleaning water drinking water synthetic cell genome project Jack Horner crowd-pleasing accountability chickenosaurus noam kostucki United States Global Issues Jurassic Park energy crisis Simon Sinek Dan Ariely tedxsanjoseca communication irrationality to psychology Zichermann Sagmeister decisions human nature filter water human genome cell biologyFrom:Davon BaltimoreViews:0 0ratingsTime:10:11More inFilm Animation

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Watch Behind The Scenes: Ted Williams Records Kraft Macaroni

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free unlocking tool for iphone 4s Free Download of Best iphone Unlocker and Jailbreaker at Link in Video. Easily Unlock your Iphone with just few clicks.Works with all models and firmwares. how to jailbreak itouch 3.1.3 with blackra1n how to unlock iphone 4 from verizon to tmobile unlock for iphone 3gs new bootrom how to unlock an iphone 4 without sim card how to unlock at t iphone 4 4.12.01 unlocking the secrets of the genome mobile iphone jailbreak best iphone 4 unlock apps how to unlock my iphone 4s free new unlock iphone 3g 3.1 3From:AutomaticPython48Views:0 0ratingsTime:01:01More inScience Technology

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The Genomics of Attention Deficit Hyperactivity Disorder - Maximillian Muenke
Nov. 2, 2012 - Genomics in Medicine Lecture Series More: http://www.genome.govFrom:GenomeTVViews:9 0ratingsTime:01:06:31More inFilm Animation

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The Genomics of Attention Deficit Hyperactivity Disorder - Maximillian Muenke - Video

Genome Lab SNP Stream Genotyping System Display
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Genome Lab SNP Stream Genotyping System Display - Video

SAN DIEGO & SAN FRANCISCO--(BUSINESS WIRE)--

Please replace the release (dated November 5, 2012) with the following corrected version due to multiple revisions.

The corrected release reads:

BIONANO GENOMICS LAUNCHES IRYS, A NOVEL PLATFORM FOR COMPLEX HUMAN GENOME ANALYSIS

Speed, Simplicity Enable Routine Use of Genetic Information in Wide-Ranging Applications

BioNano Genomics today announced the commercial rollout of its breakthrough Irys System, an intuitively designed genome mapping system that empowers genomics researchers with a new way of analyzing genomic DNA. Irys makes it possible to routinely and accurately detect genomic structural variation and to finish genome assemblies.

(Note to editors: See associated image.)

Irys reveals genome architecture in its native state, thereby adding a completely new repertoire to the genomics tool kit. The Irys System allows researchers and clinicians to access meaningful biological information that is disrupted or completely lost when samples are analyzed by the methods used today such as next-generation sequencing or microarrays, said BioNano Genomics President and CEO Dr. R. Erik Holmlin, who announced the launch of Irys from the American Society of Human Genetics (ASHG) Annual Meeting, being held in San Francisco, Nov. 6-10. BioNano Genomics is excited about introducing a new approach that makes it easy to observe genomic architecture and context. We believe this capability will add unprecedented insight into biology and usher in a new wave of discoveries.

The fully automated Irys benchtop instrument uses the IrysChip to uncoil and confine long DNA molecules in proprietary Nanochannel Arrays where they are uniformly linearized in a highly parallel display for high-resolution, single-molecule imaging. Irys does not employ DNA fragmentation or amplification, which are typical with next-generation sequencing. The result is sequence information over extremely long reads ranging from hundreds of kilobases to a megabase, where the samples valuable structural information is preserved. Irys makes it possible for researchers to directly observe structural variants including replications, deletions, translocations and inversions. The simplicity, affordability and speed of Irys, which can analyze several gigabases per hour, make it an ideal genome mapping solution for labs of any size, said Todd Dickinson, VP Commercial Operations, and we envision broad application throughout genomics and epigenomics, especially in biomedical research and ultimately molecular diagnostics.

Complex genomes contain highly repetitive sequences and prove challenging for whole genome assembly, said Pui-Yan Kwok, MD, PhD, Henry Bachrach Distinguished Professor at the UCSF School of Medicine and senior author of a study published in Nature Biotechnology, which demonstrated the utility of the Irys platform for structural variation analysis and de novo assembly of next generation sequencing (NGS) data. The BioNano approach to genome mapping readily resolves these issues, and allowed us to achieve haplotype-resolved de novo assembly of the notoriously difficult human MHC region. We are thrilled with the quality of data we are getting with the Irys system and are now deploying this new technology broadly across our research program.

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CORRECTING and REPLACING BioNano Genomics Launches Irys, a Novel Platform for Complex Human Genome Analysis

SAN DIEGO & SAN FRANCISCO--(BUSINESS WIRE)--

BioNano Genomics today released its breakthrough Irys System, an intuitively designed genome mapping system that empowers genomics researchers with a new way of achieving more accurate and comprehensive discoveries, including structural variation analysis and sequence assemblies.

(Note to editors: See associated image.)

Irys is a novel, automated platform that uses single-molecule imaging to visualize extremely long nucleic acids and reveal genome architecture in its native state, thereby significantly extending the reach of existing genomic technologies.

The Irys System allows researchers and clinicians to access meaningful biological information that is often disrupted or completely lost when molecules are sheared, said BioNano Genomics President and CEO Dr. R. Erik Holmlin, who announced the launch of Irys at the American Society of Human Genetics (ASHG) Annual Meeting, being held in San Francisco Nov. 6-10. BioNano Genomics is pleased to introduce a new approach that allows one to easily observe architecture and context across the whole genome, providing unprecedented insight into biology.

The fully automated Irys benchtop instrument uses a proprietary IrysChip to uncoil and confine long DNA molecules into nanochannels, uniformly linearizing them for high-resolution, single-molecule imaging. The Irys System does not require DNA fragmentation and amplification steps that are typical of next-generation sequencing resulting in extremely long reads of hundreds of kilobases to megabases. Because of this, the samples valuable structural information is preserved, making it possible for researchers to directly observe structural variants including translocations and inversions.

The simplicity, affordability and speed of Irys, which can analyze several gigabases of data per hour, make it an ideal genome mapping solution for labs of any size, said Todd Dickinson, Vice President of Commercial Operations for BioNano Genomics. We envision broad applications throughout biomedical research and ultimately molecular diagnostics.

Complex genomes contain highly repetitive sequences and prove challenging for whole genome assembly, said Pui-Yan Kwok, MD, PhD, Henry Bachrach Distinguished Professor at the University of California, San Francisco School of Medicine and senior author of a study published in Nature Biotechnology, which demonstrated the utility of the Irys platform for structural variation analysis and de novo assembly of next generation sequencing (NGS) data. The BioNano approach to genome mapping readily handled these issues, and allowed us to achieve haplotype-resolved de novo assembly of the notoriously difficult human MHC region. We are thrilled with the quality of data we are getting with the Irys system and are now deploying this new technology broadly across our research program.

Dr. Kwok will join Dr. Holmlin and other experts at ASHG to lead an educational workshop about Irys at 12:45 p.m. on Nov. 8 at Moscone Center, Room 301. Register to attend the workshop to learn more about the new system, or visit BioNano Genomics Booth 924/926 on the ASHG expo floor.

About BioNano Genomics

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BioNano Genomics Launches Irys, a Novel Platform for Complex Human Genome Analysis

After decades of hard work, the barley genome, or genetic code, has been cracked.

The barley genome is twice the size of our own human genome and was successfully ordered and assembled by an international group of scientists ranging from many different scientific disciplines.

The International Barley Sequencing Consortium is the group of scientist who cracked the genetic code of the 5.3 billion lettered barley genome, and the research was published in the most recent edition of Nature.

This consortium was created in 2006 and is a collaboration of scientists from 22 different organizations in nine different countries.

Roger Wise, research plant geneticist for United States Department of Agriculture-Agricultural Research Service and collaborator professor of plant pathology at Iowa State was one of these scientists.

This project was absolutely huge, and this is reflected by the well over 60 authors on the paper, Wise said.

Records indicate that barley has been around and developing for more than 10,000 years, originating in modern-day Middle East.

Today, barley ranks fourth among the cereals in worldwide production, behind wheat, rice and corn.

According to the National Barely Growers Association, 320 million bushels of barley were produced each year in the United States from 1994 till 2003, averaging $760 million dollars in the agricultural economy.

This research is the first of many steps to bring an increase in yields, improve pest and disease resistance, and enhance nutritional value to barley.

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Barley genome gives insight into future pest and disease resistance

BEVERLY, Mass.--(BUSINESS WIRE)--

BIOBASE GmbH announced today that it has been selected by Cypher Genomics to aid in whole genome interpretation. Researchers at Cypher Genomics will incorporate the knowledgebase in Genome TraxTM to assist in their interpretation of next generation sequencing variants to provide rich genomic knowledge from sequencing data.

Cypher Genomics provides comprehensive automated software solutions for medical geneticists, computational biologists, clinicians, and researchers looking to extract maximal value from whole genome sequencing. Genome TraxTM enables the ability to interpret next generation-sequencing (NGS) data and convert the genomic data to actionable genomic knowledge.

Genome TraxTM prioritizes human genome variants in whole genome or exome data that merit further investigation. The tool maps NGS data to known features such as HGMD disease mutations and TRANSFAC regulatory sites. In addition, Genome TraxTM identifies novel mutations that are likely to affect the function of candidate disease genes, and enables users to filter out the millions of irrelevant variants.

"Genome TraxTM provides the most comprehensive database of human disease associations and is an invaluable resource in both clinical and research-grade genetics and genomics activities," explains Dr. Ali Torkamani, Chief Science Officer, at Cypher Genomics.

"Cypher Genomics will interpret genomes with cutting-edge precision and enable the use of genomics in diagnosis, discovery, and treatment. Genome TraxTM frees them to focus on their deep expertise in computer science, quantitative genetics, and medicine, to deliver state-of-the-art genome processing to their customers," stated Frank Schacherer, CTO, BIOBASE.

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Cypher Genomics Selects BIOBASE Genome TraxTM Knowledgebase for Variant Analysis