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GenomeQuest Hosting Seminar at ABRF Conference In Sacramento, CA
Date:3/4/2010

can compare and mine their sequence data, annotations, and findings across millions of reads -- from a simple web-browser
-Import sequence-read data and reference genome data from a wide variety of sources, including the world's largest collection of sequence reference databases
-Launch the different workflows and connected tools, discussing parameter settings, and analyzing their results
Share and aggregate results through ‘physical’ and "virtual" databases
How to work with instruments from LIFE, Illumina, and other popular providers

Topics for Developers (including bioinformaticians and computational biologists):

-Configure and customize SDM to support all research and clinical workflows
-Unify and cloud-enable SDM across users, instruments, tools, databases, projects, and organizations
-Scale their SDM to NGS and secure, cloud-level sharing of sequence data and results
-Address the high-performance and scalability demands of NGS
-Review the full range and listing of API services: engine-level, workflow-level, and cloud-level
-Understand the GQ-Engine basics, including its multi-algorithm alignment/comparison, built-in parallelism, and unified sequence/annotation data model
-Understand how developers can innovate on the cloud and securely publish workflows and applications to extended communities

Presenter: Richard Resnick, VP of Software & Services, GenomeQuest, Inc.
Registration Online: www.genomequest.com/ABRFseminar

Contact:
Dana Wormer
1.215.888.0960

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Read the full story at http://www.prweb.com/releases/GenomeQuest/Sacramento_Seminar/prweb3684744.htm.


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