Corporate Banner
Satellite Banner
Informatics
Scientific Community
 
Become a Member | Sign in
Home>News>This Article
  News
Return

Affordable, Cloud-Based DNA Sequencing Service Announced

Published: Thursday, April 26, 2012
Last Updated: Thursday, April 26, 2012
Bookmark and Share
BGI's EasyGenomics service brings era of affordable, personalized medicine a step closer to reality.

NVIDIA today announced that BGI, the world's largest genomics institute, is launching a service that will enable researchers worldwide to perform affordable next-generation sequencing (NGS) bioinformatics analysis in the cloud.

The new "EasyGenomics" service from Shenzhen, China-based BGI combines an intuitive user interface with BGI's automated pipeline analysis, software and tools. These are integrated with the industry's largest sequencing platform to provide everything biologists, bioinformaticists and, ultimately, physicians need to submit and receive an automated analysis of DNA sequencing data.

Accelerated by NVIDIA GPUs, which speed the processing of the analysis of DNA big data from days to hours compared with a CPU-based system, EasyGenomics dramatically expands the availability of advanced genomics research capabilities to researchers around the world, bringing science closer to an era of affordable and viable personalized medicine.

BGI is launching a limited free trial of the new service today for qualified biologists and bioinformaticists at the 2012 Bio-IT World Conference and Expo. To learn more or to apply, visit the EasyGenomics website.

"By enabling larger numbers of researchers to accelerate DNA sequencing data more easily and affordably, we hope to help facilitate the use of genomics for clinical diagnostics as a practical component of health care, as well as for complex disease research," said Dr. Lin Fang, vice president at BGI. "GPU acceleration enables scientists to analyze DNA sequencing data faster than was ever possible, reducing the time from five days to just five hours. Once fully deployed in the cloud, we anticipate EasyGenomics could one day revolutionize genomics research."

The EasyGenomics cloud service features hybrid computing systems powered by NVIDIA(R) Tesla(R) M2070 and M2075 GPUs, which accelerate the DNA sequencing data analysis in conjunction with system CPUs. BGI plans to upgrade the EasyGenomics service with hundreds of additional NVIDIA Tesla GPUs when it is fully deployed, at which time it is expected to support thousands of users.

"This could be the year of the $1,000 genome due to rapid decline in sequencing costs. We will soon be drowning in a deluge of data from the genome sequencers," said Sumit Gupta, senior director of the Tesla business at NVIDIA. "BGI's EasyGenomics service uses the power of GPU computing to provide an affordable and easy-to-use method for scientists to crunch through this new genomics big data problem and get us that much closer to effective and affordable individualized treatments."


Further Information
Access to this exclusive content is for Technology Networks Premium members only.

Join Technology Networks Premium for free access to:

  • Exclusive articles
  • Presentations from international conferences
  • Over 2,400+ scientific posters on ePosters
  • More than 3,700+ scientific videos on LabTube
  • 35 community eNewsletters


Sign In



Forgotten your details? Click Here
If you are not a member you can join here

*Please note: By logging into TechnologyNetworks.com you agree to accept the use of cookies. To find out more about the cookies we use and how to delete them, see our privacy policy.

Related Content

BGI-BOX Terminal Server Debut Operation in China Agricultural University
BGI’s first cloud computing terminal server allows users to access bioinformatics analysis and genomic data in their own laboratories with the advantages of easy to use, high flexibility and user-friendly interface.
Monday, December 19, 2011
Scientific News
The Mystery of the Instant Noodle Chromosomes
Researchers from the Lomonosov Moscow State University evaluated the benefits of placing the DNA on the principle of spaghetti.
Web App Helps Researchers Explore Cancer Genetics
Brown University computer scientists have developed a new interactive tool to help researchers and clinicians explore the genetic underpinnings of cancer.
An Innovative Algorithm to Decipher How Drugs Work Inside the Body
Researchers at Columbia University Medical Center (CUMC) have developed a computer algorithm that is helping scientists see how drugs produce pharmacological effects inside the body.
How do Networks Shape the Spread of Disease and Gossip?
A team of mathematicians from Oxford University, University of North Carolina at Chapel Hill, and Rutgers University used a set of mathematical rules to encode how a contagion spreads, and then studied the outcomes of these rules.
AncestryDNA and Calico to Research the Genetics of Human Lifespan
Collaboration will analyze family history and genetics to facilitate development of cutting-edge therapeutics.
Informatics Tool Helps Scientists Prioritize Protein Modification Research
Researchers have developed a new informatics technology that analyzes existing data repositories of protein modifications and 3D protein structures to help scientists identify and target research on "hotspots" most likely to be important for biological function.
Software Differences can Skew Medical Scan Results
Differences in software can significantly skew results of medical scans commonly used in clinical care and research.
AMRI, PerkinElmer to Collaborate on Drug Discovery
Albany Molecular Research (AMRI) and PerkinElmer are collaborating to provide drug discovery infrastructure and services in AMRI's newly launched drug discovery center.
Exploring Living cells
JPK reports the exploration of living cells using nanoscale and single molecule techniques through the application of scanning probe microscopy.
Vulnerabilities in Genome's 'Dimmer Switches' Should Shed Light on Hundreds of Complex Diseases
Up to one-fifth of human DNA act as dimmer switches for nearby genes, but scientists have long been unable to identify precisely which mutations in these genetic control regions really matter in causing common diseases.
Scroll Up
Scroll Down
Skyscraper Banner

Skyscraper Banner
Go to LabTube
Go to eposters
 
Access to the latest scientific news
Exclusive articles
Upload and share your posters on ePosters
Latest presentations and webinars
View a library of 1,800+ scientific and medical posters
2,400+ scientific and medical posters
A library of 2,500+ scientific videos on LabTube
3,700+ scientific videos
Close
Premium CrownJOIN TECHNOLOGY NETWORKS PREMIUM FREE!