Genomic sequences processed in minutes, rather than weeksJune 22, 2005Breakthrough could lead to solving complex problems related to human biology, biological threats and the environment RICHLAND, WA - A new computational tool developed at the Department of Energy's Pacific Northwest National Laboratory is speeding up our understanding of the machinery of life - bringing us one step closer to curing diseases, finding safer ways to clean the environment and protecting the country against biological threats. ScalaBLAST is a sophisticated "sequence alignment tool" that can divide the work of analyzing biological data into manageable fragments so large data sets can run on many processors simultaneously. The technology means large-scale problems - such as the analysis of an organism - can be solved in minutes, rather than weeks.
In the world of high-end computing, researchers assemble systems composed of many processors. For example, PNNL's supercomputer has 1,960 processors - a big machine with lots of memory and the ability to tackle large problems. However, without special modifications, software doesn't run any faster on it than it would on a personal computer. In order to get answers to complicated biological questions more quickly, PNNL researchers "parallelized" the software using Global Arrays, a powerful programming toolkit, by creating algorithms to divvy up the work. PNNL researchers say ScalaBLAST may be used to process complex genomic sequences, work that is essential to understanding the building blocks of the genome - or rather, how they work and fit together. Genomes represent an organism's entire DNA, including its genes. When the gene's sequences are analyzed they can provide clues to diseases and possible treatments. Using ScalaBLAST, researchers can manage the large influx of data resulting from new questions that arise during human genome research. Prior to this new tool, it took researchers 10 days to analyze one organism. Now, researchers can analyze 13 organisms within nine hours, making the time-to-solution hundreds of times faster. "Access to and understanding the pieces of genome sequences will allow researchers to understand the body's cellular machinery and discover clues to some types of cancer. And it will help in developing drugs or detection methods to be used for particular diseases," said T.P. Straatsma, a PNNL senior research scientist. And it likely will help in other areas of human health. It's fair to say that, in the realm of human health and disease, if you can solve a problem in one area, you can often solve it in others - that's the nature of human biology,\\\\\\\ Pacific Northwest National Laboratory | |||||||||||||||||||||
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Related Genomic Sequence News Articles Cold Spring Harbor Scientists Devise Novel, Low-Cost Method of Sifting Genome's High-Value Regions Scientists at Cold Spring Harbor Laboratory (CSHL) have developed a new means of extracting and interpreting data from the human genome that is more powerful and more economical than methods currently employed. Identified main genetic variants involved in response to HIV This international collaboration has been the largest ever to have taken place in a large scale study on genetic differences between patients infected by HIV, and is the first study of this kind in the field of infectious disease. One man's junk may be a genomic treasure Scientists have only recently begun to speculate that what's referred to as "junk" DNA - the 96 percent of the human genome that doesn't encode for proteins and previously seemed to have no useful purpose - is present in the genome for an important reason. 454 Life Sciences and Baylor College of Medicine complete sequencing of DNA pioneer 454 Life Sciences Corporation, in collaboration with scientists at the Human Genome Sequencing Center, Baylor College of Medicine, announced today in Houston, Texas, the completion of a project to sequence the genome of James D. Watson, Ph.D., co-discoverer of the double-helix structure of DNA. Researchers create interactive map with Google technology to track avian flu spread An interactive "supermap" that portrays the mutations and spread of the avian flu around the globe over time should help researchers and policy makers better understand the virus and anticipate further outbreaks, according to a new study involving University of Colorado at Boulder and Ohio State University researchers. Quick diagnosis of flu strains possible with new microchip test Scientists from the University of Colorado at Boulder and the Centers for Disease Control and Prevention (CDC) have developed a microchip-based test that may allow more labs to diagnose influenza infections and learn more about the viruses causing illness. Scientists discover a genetic code for organizing DNA within the nucleus DNA - the long, thin molecule that carries our hereditary material - is compressed around protein scaffolding in the cell nucleus into tiny spheres called nucleosomes. Cracking the genetic code for control of gene expression Molecular biologists, developmental biologists and computer scientists at the Universtity of Helsinki, Finland, came together to advance towards cracking the code for how gene expression is controlled. Researchers predict infinite genomes Ever since the genomics revolution took off, scientists have been busily deciphering vast numbers of genomes. Cataloging. Analyzing. Comparing. Public databases hold 239 complete bacterial genomes alone. Genome study of beneficial microbe may help boost plant health In a study expected to greatly benefit crop plants, scientists have deciphered the genome of a root- and seed-dwelling bacterium that protects plants from diseases. More Genomic Sequence News Articles |
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