from UT San Diego By Bradley J. Fikes

A super-fast genome processor called the Dragen Bio-IT Processor is now on sale by San Diego’s Edico Genome. The processor, which is sold on a standard PCIe computer board, is meant to relieve the bottleneck in analyzing the flood of genomic data.
The Dragen processor is a special-purpose microprocessor adapted to analyzing the human genome, said Pieter van Rooyen, Edico’s chief executive. That enables the accelerator card to outperform general-purpose computer chips, such as those used in servers now used to characterize genomic data.
Gene sequencing technology cuts genetic material into fragments, determines the sequence of each fragment, then reassembles these fragments like an immensely complicated jigsaw puzzle.
Software algorithms and high-powered clusters of computers are now used to do that reassembling, but it takes many hours, van Rooyen said. A human genome has 3 billion base pairs, or DNA letters.
To produce a medical-grade genome, each genome is read and reassembled more than 30 times, and the results compared to reduce errors. Each genome is compared to a reference genome.
“What we’ve done is take that processing that needs to be done to reassemble that giant jigsaw puzzle, and put it in a chip,” van Rooyen said.
“The chip does secondary processing. It does all the processing to map those reads, figure out where they came from, stack them up, compensate for the errors, and then identify how are you different from the reference (genome). Do you have a mutation in one of your genes that might cause cancer? Or if you have cancer, what type do you have?”
“My team’s use of the Dragen processor has enabled us to analyze our RNA-seq data more than 60 fold faster than a 16-core CPU,” said Gene Yeo, of the Cellular and Molecular Medicine and Institute for Genomic Medicine, University of California San Diego, in an Edico statement.
Dragen processor discussion with Dr. Eric Topol
Topol discusses the Dragen processor with Edico Genome CEO Pieter van Rooyen.
Yeo said the processor has shortened analysis times from 12 minutes down to 11 seconds per RNA sequence dataset, with the same accuracy standard software.
Source – UT San Diego
from UT San Diego By Bradley J. Fikes
A super-fast genome processor called the Dragen Bio-IT Processor is now on sale by San Diego’s Edico Genome. The processor, which is sold on a standard PCIe computer board, is meant to relieve the bottleneck in analyzing the flood of genomic data.
The Dragen processor is a special-purpose microprocessor adapted to analyzing the human genome, said Pieter van Rooyen, Edico’s chief executive. That enables the accelerator card to outperform general-purpose computer chips, such as those used in servers now used to characterize genomic data.
Gene sequencing technology cuts genetic material into fragments, determines the sequence of each fragment, then reassembles these fragments like an immensely complicated jigsaw puzzle.
Software algorithms and high-powered clusters of computers are now used to do that reassembling, but it takes many hours, van Rooyen said. A human genome has 3 billion base pairs, or DNA letters.
To produce a medical-grade genome, each genome is read and reassembled more than 30 times, and the results compared to reduce errors. Each genome is compared to a reference genome.
Dragen processor discussion with Dr. Eric Topol
Topol discusses the Dragen processor with Edico Genome CEO Pieter van Rooyen.
Yeo said the processor has shortened analysis times from 12 minutes down to 11 seconds per RNA sequence dataset, with the same accuracy standard software.
Source – UT San Diego
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from UT San Diego By Bradley J. Fikes
A super-fast genome processor called the Dragen Bio-IT Processor is now on sale by San Diego’s Edico Genome. The processor, which is sold on a standard PCIe computer board, is meant to relieve the bottleneck in analyzing the flood of genomic data.
The Dragen processor is a special-purpose microprocessor adapted to analyzing the human genome, said Pieter van Rooyen, Edico’s chief executive. That enables the accelerator card to outperform general-purpose computer chips, such as those used in servers now used to characterize genomic data.
Gene sequencing technology cuts genetic material into fragments, determines the sequence of each fragment, then reassembles these fragments like an immensely complicated jigsaw puzzle.
Software algorithms and high-powered clusters of computers are now used to do that reassembling, but it takes many hours, van Rooyen said. A human genome has 3 billion base pairs, or DNA letters.
To produce a medical-grade genome, each genome is read and reassembled more than 30 times, and the results compared to reduce errors. Each genome is compared to a reference genome.
Dragen processor discussion with Dr. Eric Topol
Topol discusses the Dragen processor with Edico Genome CEO Pieter van Rooyen.
Yeo said the processor has shortened analysis times from 12 minutes down to 11 seconds per RNA sequence dataset, with the same accuracy standard software.
Source – UT San Diego
Related Posts
RNA Sequencing identifies new tick-borne virus that causes flu-like illness
Worm’s radical transformation shows metamorphosis can change the functions of cells
RNA sequencing reveals functional chimeric mRNAs in mammalian immunity
Atlas of the brain’s striatum could guide researchers to new drug treatments
Immune cells offer insights on billion-dollar virus
A functionally integrated cross-tissue alternative splicing program during short-term calorie restriction
Dietary oxidized plant sterol shifts macrophage state to fuel aortic inflammation
Unlocking the past – new method helps gain insights into old tissue
Novel AI model trained on RNA-Seq data accurately detects key gene mutations and predicts biomarkers across 32 cancer types
Transcriptomic aging clock reveals age-related molecular patterns in opioid dependence
RNA sequencing helps predict stem cell transplant benefit in pediatric AML
Protein ‘switch’ determines whether liposarcoma cells will become aggressive
Precursor tRNAs sense temperature changes: heat stress-induced capped pre-tRNAs suppress protein synthesis
Ketamine increases neuroplasticity in female mice but not in males
Somatic mutations linked to vascular damage in progeria
Scientists map dormant cancer cells’ hideouts, opening new targets for treatment
Soluble signals released by neighboring cells direct how the human kidney is built
Genetics influence how cancer arises – and how it evolves
RNA-based testing uncovers extraordinary diversity in mutations driving lung cancer
Study offers new insights into why ex-smokers remain at elevated risk of lung disease
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