Next Generation Sequencing for Research and Genomics - Session IIIBMonday, September 19, 2011, 13:00 - 17:30Next Generation Sequencing for Research and Genomics - Session III A Data analysis
T. Schwei*
DNA Star (Madison, US)
13:00 – 13:45 Building molecular networks of disease from NGS data
E. Stupka* San Raffaele Scientific Institute (Milan, IT)
13:45 – 14:30 Influenza – Nucleid acids to digital genome
T. Stockwell* J. Craig Venter Institute (Rockville, US)
14:30 – 14:45 Break
14:45 – 15:30 Galaxy for high-throughput NGS analysis
D. Blankenberg* Penn State University (University Park, US)
15:30 – 15:45 DNASTAR Software: Assembly & analysis
T. Schwei* DNA Star (Madison, US)
15:45 – 16:00 Accurate genome variant detection using Omixon
A. Berces* Omixon (Budapest, HU)
16:00 – 16:15 Data Analysis Your Way with Pipeline Pilot
R. Dunn* Accelrys (San Diego, US)
16:15 – 16:30 Break
16:30 – 16:45 SSPACE and gap closure
W. Pirovano* BaseClear (Leiden, NL)
16:45 – 17:30 Informatics challenges in cancer genomes
P. Boutros* International Cancer Genome Consortium (ICGC) (Toronto, CA)
17:30 – 17:45 Break
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