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

Illumina Announces BaseSpace® Pricing for Data Storage and Processing

Published: Thursday, December 27, 2012
Last Updated: Thursday, December 27, 2012
Bookmark and Share
Breaks analysis cost bottleneck for next generation sequencing workflow.

Illumina, Inc. has announced pricing for BaseSpace, the Company’s genomics cloud computing and storage platform.

The flexible pricing structure will allow researchers around the world to take advantage of BaseSpace’s industry-leading data storage, analysis, and sharing capabilities.

Every BaseSpace account will now include 1 terabyte (TB) of free storage for Illumina data, enabling MiSeq® system users to store hundreds of runs and HiSeq® system users to store several runs worth of data, providing a risk-free means to get started with the cloud.

Included with the 1 terabyte of storage is free alignment and variant detection for all Illumina data, eliminating what is currently one of the more costly steps in sequencing.

BaseSpace users will also have the ability to purchase incremental storage from within BaseSpace, in both monthly and annual durations.

In the fall, through BaseSpace Apps, every BaseSpace user will have the ability to run analysis applications on an “as-needed” basis, developed by both open source and third-party developers.

These applications can be purchased “on the fly” and per analysis, allowing users to affordably run new analysis strategies without investing in dedicated software or hardware infrastructure.

BaseSpace Apps will include a diverse and growing set of industry leading data analysis and visualization applications for both MiSeq and HiSeq data analysis. The price for running a BaseSpace App will be set directly by each developer.

“Illumina is taking huge strides to eliminate the much publicized ‘data deluge’ and data analysis bottleneck. The adoption of BaseSpace thus far has been exciting to watch, with the vast majority of MiSeq systems now connected, and already half of those actively uploading data," said Alex Dickinson, Illumina's Senior Vice President, Cloud Genomics.

Dickinson continued, “Making BaseSpace accessible to more researchers will have far-reaching effects, enabling more investment in understanding biology and less in processing data."

“BaseSpace has made it easy to share data with our collaborators and customers,” said Dr. James Hadfield of the Cambridge Research Institute, United Kingdom. “We are looking forward to the development and integration of analysis tools and to using BaseSpace for HiSeq.”

Already compatible with Illumina’s MiSeq system, BaseSpace will become available for use with the Company’s HiSeq systems early in the fourth quarter of 2012, offering the same benefits of seamless real-time data transfer, assembly and variant detection for fast, high quality genome processing. BaseSpace Apps will also become available to customers in the fourth quarter.


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

Illumina Names Sanjay Chikarmane as SVP and General Manager
Chikarmane will report to Illumina President, Francis deSouza.
Tuesday, July 21, 2015
Discordant NIPT Test Results May Reflect Presence of Maternal Cancer
Results published in Journal of the American Medical Association.
Tuesday, July 14, 2015
Biomed Realty and Illumina Announce New Build-to-Suit Laboratory Building
New building to be located in scientific research park, Granta Park, and will serve as Illumina’s new European headquarters.
Friday, June 26, 2015
Annoroad and Illumina to Co-Develop NGS Diagnostic System
Both Companies have entered into an agreement to jointly develop advanced clinical applications for reproductive health.
Thursday, June 11, 2015
Illumina, Merck KGaA and Genea Form the Global Fertility Alliance
Global fertility alliance will identify and work on improvements of fertility-related laboratory processes.
Tuesday, June 09, 2015
Illumina Files New Patent Infringement Suit
Company has filed a new suit against Ariosa Diagnostics, Inc. and Roche Molecular Systems, Inc.
Tuesday, May 19, 2015
The Agrigenomics Market
Exponential population growth and changing climate patterns are creating unique challenges for the agriculture industry. To continue to address global food needs, many researchers, breeders, and farms are turning to genomics, or DNA science, to optimize production.
Thursday, May 07, 2015
Berry Genomics NextSeq CN500 Instrument Receives CFDA Premarket Clearance
Products collaboratively developed by Berry Genomics and Illumina Serve Chinese clinical NIPT market.
Wednesday, April 01, 2015
Illumina Accelerator Secures $40 Million Boost Capital to Back New Graduates
Obtains commitment from viking global investors to advance genomics startups.
Friday, February 27, 2015
Lockheed Martin and Illumina to Collaborate
New strategic alliance to collaborate on developing genomics solutions to improve public health and wellness.
Tuesday, January 13, 2015
£15m Initiative Puts Scotland at Forefront of Gene-Led Healthcare
Initiative sees the Universities of Edinburgh and Glasgow partner with Illumina.
Monday, January 12, 2015
Illumina Announces Oncology CDx Partnership with AstraZeneca, Janssen and Sanofi
Illumina, forms collaborative partnerships with leading pharmaceutical companies to develop a universal next-generation sequencing (NGS)-based oncology test system.
Thursday, August 21, 2014
Illumina Appoints Jeff Huber to its Board of Directors
Mr. Huber is Senior Vice President at Google Inc.
Friday, August 01, 2014
UK to Invest £300M in 100,000 Genomes Project with Illumina as Key Partner
The four year project will allow scientists to do pioneering new research to decode 100,000 human genomes.
Friday, August 01, 2014
Berry, Illumina Co-Develop NGS System for CFDA Review and Approval
Berry Genomics will use Illumina’s NGS technology to secure Chinese Food and Drug Administration regulatory approval for clinical applications, expanding access to NGS-based tests in China.
Monday, July 21, 2014
Scientific News
Long Telomeres Associated with Increased Lung Cancer Risk
Genetic predisposition for long telomeres predicts increased lung adenocarcinoma risk.
Expanding the Brain
A team of researchers has identified more than 40 new “imprinted” genes, in which either the maternal or paternal copy of a gene is expressed while the other is silenced.
Identifying a Key Growth Factor in Cell Proliferation
Researchers discover that aspartate is a limiter of cell proliferation.
Study Uncovers Target for Preventing Huntington’s Disease
Scientists from Cardiff University believe that a treatment to prevent or delay the symptoms of Huntington’s disease could now be much closer, following a major breakthrough.
The Genetic Roots of Adolescent Scoliosis
Scientists at the RIKEN Center for Integrative Medical Sciences in collaboration with Keio University in Japan have discovered a gene that is linked to susceptibility of Scoliosis.
A Gene-Sequence Swap Using CRISPR to Cure Haemophilia
For the first time chromosomal defects responsible for hemophilia have been corrected in patient-specific iPSCs using CRISPR-Cas9 nucleases
New Tool Uses 'Drug Spillover' to Match Cancer Patients with Treatments
Researchers have developed a new tool that improves the ability to match drugs to disease: the Kinase Addiction Ranker (KAR) predicts what genetics are truly driving the cancer in any population of cells and chooses the best "kinase inhibitor" to silence these dangerous genetic causes of disease.
Understanding the Molecular Origin of Epigenetic Markers
Researchers at IRB Barcelona discover the molecular mechanism that determines how epigenetic markers influence gene expression.
New Tech Enables Epigenomic Analysis with a Mere 100 Cells
A new technology that will dramatically enhance investigations of epigenomes, the machinery that turns on and off genes and a very prominent field of study in diseases such as stem cell differentiation, inflammation and cancer has been developed by researchers at Virginia Tech.
Access Denied: Leukemia Thwarted by Cutting Off Link to Environmental Support
A new study reveals a protein’s critical – and previously unknown -- role in the development and progression of acute myeloid leukemia (AML), a fast-growing and extremely difficult-to-treat blood cancer.
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!