Category Archives: Genome

De Novo Genome Assembly in Lasergene Genomics Suite
DNASTAR #39;s Lasergene Genomics Suite includes de novo sequence assembly software that allows users to quickly and easily perform de novo assemblies using either long or short reads from all major next-gen sequencing platforms. Features of the Lasergene Genomics Suite software include: - Quick and accurate de novo assembly on a desktop computer - Assembly of either single-end or paired-end data - The ability to view contig scaffolds along with the paired sequences that tie the contigs together - Annotation of gaps in the scaffold consensusFrom:DNASTARIncViews:0 0ratingsTime:01:36More inScience Technology

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Insom The Raving Religion Promo Mix December 2012
Insom aka Gabriel Mentis was born in 1987 and raised in Athens, Greece. From an early age he got a taste for music learning to play the piano and violin, until 2002 when he discovered Cubase. After a while of learning how to lay down beats he started producing drum bass, mostly neurofunk releasing his first free EP #39;Fire #39; in 2009. In 2011 Insom had his first official release with the track #39;Times of Terror #39;, which came out on Germany #39;s biggest drum bass label Trust In Music on their Last Second Chance EP. Since then he has gone on to have releases on Ammunition, Close to Death, Genome, VIM, Dephunked, In Da Jungle, Melting Pot and Extent Recordings. Insom is also part of Urban Danja and Dub Riots and is also known to produce dubstep, breaks, hip hop beats for mc #39;s and experimental sounds. To keep updated with Insom #39;s latest news and events check out his pages. Turn up the volume and enjoy! Insom http://www.facebook.com http://www.mixcloud.com http://www.youtube.com twitter.com insom.bandcamp.comFrom:TheRavingReligionViews:1 0ratingsTime:51:09More inMusic

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Principles of Clinical
Buy from Amazon CA Site http://www.amazon.ca Product Description Principles of Clinical Advances in genetics are transforming estimates of an individual #39;s risk of developing cancer and approaches to prevention and management of cancer in those who may have increased susceptibility. Identifying and caring for patients with hereditary cancer syndromes and their family members present a complex clinical, scientific and social challenge. This textbook, by leading experts at Massachusetts General Hospital Cancer Center, highlights the current understanding of the genetics of hereditary cancers of the breast, ovary, colorectum, stomach, pancreas, kidney, skin, and endocrine organs. Practical guidelines for the use of genetic testing, cancer screening and surveillance, prophylactic surgery, and promising targeted therapeutic agents are discussed.In addition, ongoing research involving genome-wide screens to identify novel modest risk-associated genetic loci are explored, along with new approaches to the application of genetic markers in guiding therapeutic options. Disclaimer: Orchid is a participant in the Amazon.ca, Inc. Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to Amazon CA Site. Amazon and the Amazon logo are trademarks of Amazon, Inc. or its affiliates.From:Amalia WelkerViews:0 0ratingsTime:00:40More inScience Technology

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Evolution of Wild
Buy from Amazon CA Site http://www.amazon.ca Product Description Evolution of Wild Wild emmer is the progenitor of most cultivated wheats and thus an important source of wheat improvement. This book draws the results from multidisciplinary studies on the ecological, genetic, genomic, agronomic, and evolutionary aspects of wild emmer, conducted at many labs around the world.It is divided into the following parts: Origin and Evolution of Wheat - Population Genetics of Wild Emmer Wheat at the Protein and DNA Levels - Genetic Resources of Wild Emmer for Wheat Improvement - Genome Organization and Genetic Mapping - Conclusions and Prospects.The authors describe the evolution of wild emmer as a model organism of a selfer in evolutionary biology, and its rich potential genetic resources for wheat improvement. Disclaimer: Orchid is a participant in the Amazon.ca, Inc. Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to Amazon CA Site. Amazon and the Amazon logo are trademarks of Amazon, Inc. or its affiliates.From:Karina HarmanViews:0 0ratingsTime:00:41More inEducation

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Statistics in Genetics
Buy from Amazon CA Site http://www.amazon.ca Product Description Statistics in Genetics Though the Genome Project will eventually result in the sequencing of the human genome, as well as the genomes of several other organisms, there will still be a need for good statistics for family studies of complex diseases. The papers in this volume are contributions by some of the leading researchers in the field to the current topics in statistical genetics. One section deals with DNA sequence matching and issues related to forensics, while another deals with statistical problems of modeling phylogenies and inferential difficulties related to the complex tree structures produced, as well as the method of coalescence. Disclaimer: Orchid is a participant in the Amazon.ca, Inc. Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to Amazon CA Site. Amazon and the Amazon logo are trademarks of Amazon, Inc. or its affiliates.From:Karina HarmanViews:0 0ratingsTime:00:42More inScience Technology

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DNA Conformation and
Buy from Amazon CA Site http://www.amazon.ca Product Description DNA Conformation and Despite remarkable progress in genome science, we are still far from a clear understanding of how genomic DNA is packaged without entanglement into a nucleus, how genes are wrapped up in chromatin, how chromatin structure is faithfully inherited from mother to daughter cells, and how the differential expression of genes is enabled in a given cell type. Exploring and answering these questions constitutes one of the next frontiers in the 21st century.We are just beginning to appreciate how Multifarious DNA structures provide additional structural and functional dimensions to chromatin organization and gene expression. DNA Conformation and Transcription is the first book that compiles the fruits of the studies that have been performed to date to solve the riddle #39;written #39; in DNA conformation ("conformation code"). This book provides a comprehensive overview of the field by covering history of the field, up-to-date topics, clarifications of present day research, and future perspective of what is still to be discovered. Thus, it serves as an invaluable source of information on the "conformation code". Disclaimer: Orchid is a participant in the Amazon.ca, Inc. Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to Amazon CA Site. Amazon and the Amazon logo are trademarks of Amazon, Inc. or its affiliates.From:Mandie WorthingtonViews:0 0ratingsTime:00:41More inScience Technology

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Eschaton - Project Mayhem 2012
This event is known as the Singularity. In the year 2045, when hyper-intelligent artificial intelligence arises, armed with advanced nanotechnology, the vastly complex, systemic problems associated with aging in humans will be resolved. Alternatively, we will be able to transfer the human mind to sturdier vessels, such as computers and robots. This is a serious proposition, and many people who are alive in your time will wind up being functionally immortal. Bio technology, and nanotechnology, give us the power to manipulate our bodies and the world around us at will, at the molecular level. Progress hyper accelerates, and every hour brings a century #39;s worth of scientific breakthroughs. Life forms will ditch Darwin and take charge of their own evolution. The human genome will become just so much code to be bug-tested and optimized and, if necessary, rewritten. Indefinite life extension will become a reality; people will die only if they choose to. Death will lose it #39;s sting once and for all. There will become the opportunity to scan your consciousness into computers and enter a virtual existence, or swap your body for immortal biomechanical machines, and light out for the edges of space as an intergalactic godling. Within a matter of centuries, human intelligence will have re-engineered and saturated all the matter in the universe. This is our destiny as a species. The manifestation of all these things is your fate. It is an unstoppable wave of progress. Like the great ...From:VeriDoctoresViews:200 12ratingsTime:08:20More inNews Politics

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EMBO Conference Series: From Functional Genomics to Systems Biology
Listen to what organisers, invited speakers and delegates were saying about this year #39;s conference. The meeting is purposely very broad and covers all aspects of functional genomic approaches to systems biology, going from the genome to phenotype.From:emblmediaViews:4 0ratingsTime:04:30More inEducation

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EMBO Conference Series: From Functional Genomics to Systems Biology - Video

Eschaton - Project Mayhem 2012 #pm2012 #eTHErSEC #OpEpoch
This event is known as the Singularity. In the year 2045, when hyper-intelligent artificial intelligence arises, armed with advanced nanotechnology, the vastly complex, systemic problems associated with aging in humans will be resolved. Alternatively, we will be able to transfer the human mind to sturdier vessels, such as computers and robots. This is a serious proposition, and many people who are alive in your time will wind up being functionally immortal. Bio technology, and nanotechnology, give us the power to manipulate our bodies and the world around us at will, at the molecular level. Progress hyper accelerates, and every hour brings a century #39;s worth of scientific breakthroughs. Life forms will ditch Darwin and take charge of their own evolution. The human genome will become just so much code to be bug-tested and optimized and, if necessary, rewritten. Indefinite life extension will become a reality; people will die only if they choose to. Death will lose it #39;s sting once and for all. There will become the opportunity to scan your consciousness into computers and enter a virtual existence, or swap your body for immortal biomechanical machines, and light out for the edges of space as an intergalactic godling. Within a matter of centuries, human intelligence will have re-engineered and saturated all the matter in the universe. This is our destiny as a species. The manifestation of all these things is your fate. It is an unstoppable wave of progress. Like the great ...From:An0nYm0u5r3v0lut10nViews:221 18ratingsTime:08:20More inNonprofits Activism

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Eschaton - Project Mayhem 2012 #pm2012 #eTHErSEC #OpEpoch - Video

KANSAS CITY, Mo., Dec. 20, 2012 /PRNewswire/ --A rapid whole genome sequencing approach developed by the Center for Pediatric Genomic Medicine at Children's Mercy Hospitals and Clinics in Kansas City, was named one of TIME magazine's Top 10 Medical Breakthroughs of 2012.

In the October issue of the journal Science Translational Medicine, Children's Mercy researchers reported a proof-of-concept process, called STAT-Seq, which used whole genome sequencing to diagnose critically ill infants. STAT-Seq uses software developed at Children's Mercy, which translates physician-entered clinical features in individual patients into a comprehensive set of relevant diseases. This software substantially automates identification of the DNA variations that can explain the child's condition. The entire process from blood draw to genome sequencing, analysis and diagnosis took approximately 50 hours. Before STAT-Seq, testing even a single gene took six weeks, often longer.

"Fifty hours. That's how long it now takes to decode and interpret a newborn baby's genome an undertaking that used to take weeks or even months," TIME reported in its Top 10 Medical Breakthroughs of 2012. "And those two days can mean the difference between life and death for a critically ill infant." The rapid genome mapping test is #7 on TIME's list.

"This test changes the paradigm for genetic sequencing and diagnosis. With the ability to decode a genome from start to finish in about two days, physicians can now rapidly apply all the appropriate medical innovations available to help those babies who need their care the most," said Stephen Kingsmore, M.B. Ch.B., D.Sc., FRCPath, Director of the Center for Pediatric Genomic Medicine at Children's Mercy. "Children's Mercy is extremely proud to be recognized by TIME for this breakthrough technology and we are excited about the benefit it will have in the care setting moving forward."

The Center plans to make STAT-Seq a routine test at Children's Mercy by next year. It is currently working at capacity to analyze data from patients at Children's Mercy as well as from other pediatric institutions across the United States and around the world. The Center is currently seeking additional funding to make the test as accessible as possible and meet the high demand.

About Children's Mercy Hospitals and Clinics

Children's Mercy Hospitals and Clinics, located in Kansas City, Mo., is one of the nation's top pediatric medical centers. The 351-bed hospital provides care for children from birth through the age of 21, and has been ranked by U.S. News & World Report as one of "America's Best Children's Hospitals." For the third time in a row, Children's Mercy has achieved Magnet nursing designation, awarded to fewer than seven percent of all hospitals nationally, for excellence in quality care. Its faculty of 600 pediatricians and researchers across more than 40 subspecialties are actively involved in clinical care, pediatric research, and educating the next generation of pediatric subspecialists. For more information about Children's Mercy and its research, visit childrensmercy.org or download our mobile phone app CMH4YOU for all phone types. For breaking news and videos, follow us on Twitter, YouTube and Facebook.

About The Center for Pediatric Genomic Medicine at Children's Mercy Hospital

The first of its kind in a pediatric setting, The Center for Pediatric Genomic Medicine combines genome, computational and analytical capabilities to bring new diagnostic and treatment options to children with genetic diseases. For more information about STAT-Seq, diagnostic tests and current research, visit http://www.pediatricgenomicmedicine.com.

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Rapid Genome Test For Infants Developed By Children's Mercy Named One Of Time's Top Medical Breakthroughs Of 2012