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Monday, 08/02/2010
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Future Directions in the Analysis of Genomic Data
Nancy Zhang, Stanford University; Terence (Terry) Paul Speed, Walter & Eliza Hall Institute of Medical Research
8:35 AM
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Mixture Regression Modeling of Next-Generation Sequencing Data
Naim Rashid, The University of North Carolina at Chapel Hill
8:35 AM
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Approximate Bayesian Inference of Bacterial Population Trees with Next-Generation Sequencing Data
Alexander V. Alekseyenko, New York University; Marc Suchard, University of California, Los Angeles
8:55 AM
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Adjusting for Transcript Length Bias in RNA-seq to Improve Downstream Analyses
Justin Wade Davis, University of Missouri
9:50 AM
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A Weighted Average Likelihood Ratio Test with Application to RNAseq Data
Peng Liu, Iowa State University; Yaqing Si, Iowa State University
10:35 AM
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Statistical Methods for Detecting Rare Variants Associated with Disease Phenotypes Using Next-Generation Sequencing Data
Xihong Lin, Harvard School of Public Health
11:00 AM
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Some Statistical Issues in the Analysis of High-Throughput Sequencing Data
Margaret Taub, The Johns Hopkins University
2:05 PM
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Wednesday, 08/04/2010
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Statistics, Technology, Epigenomics, and Our Future
Rebecca W. Doerge, Purdue University; Paul Auer, Purdue University
10:35 AM
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Detecting Alternative Splicing with RNAseq
Elizabeth Purdom, University of California, Berkeley
11:00 AM
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Exploring the 1000 Genomes Project with Bioconductor
Vincent James Carey, Harvard Medical School
11:05 AM
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Understanding Immune Response with mRNA-SEQ Gene Expression Data
Ann Oberg, Mayo Clinic; Diane Grill, Mayo Clinic; Brian Bot, Mayo Clinic; Yan Asmann, Mayo Clinic; Gregory Poland, Mayo Clinic; Terry Therneau, Mayo Clinic
11:25 AM
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Thursday, 08/05/2010
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A Novel Genome Continuum Model for Sequence-Based Association Studies
Li Luo, The University of Texas School of Public Health; Momiao Xiong, The University of Texas School of Public Health
8:35 AM
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Inferring Alternative Splicing Gene Expression from Nextgen Sequencing Studies
David Rossell, IRB Barcelona
8:50 AM
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Cost-Effective Combinatorial Design for Rare-Disease Carrier Screen Using Next-Generation Sequencing Technology
Lingling An, The University of Arizona; Dear Pookhao, The University of Arizona
9:05 AM
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The GNUMAP Project: Probabilistic Mapping of Next-Generation Sequencing Reads with Applications
W. Evan Johnson, Brigham Young University; Nathan Clement, Brigham Young University; Mark Clement, Brigham Young University; Quinn Snell, Brigham Young University
9:50 AM
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Genome-Wide Detecting Differential Epigenetic/Genetic Changes Using Next-Gen Sequencing Data
Weichun Huang, National Institute of Environmental Health Sciences; Nicole V. Jordan, The University of North Carolina at Chapel Hill; Amy N. Abell, The University of North Carolina at Chapel Hill; Gary L. Johnson, The University of North Carolina at Chapel Hill; Leping Li, National Institute of Environmental Health Sciences
11:35 AM
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Statistical Methods of Exon Resequencing for Detecting Associations with Rare Variants
Judy Zhong, Sage Bionetworks; Charles Kooperberg, Fred Hutchinson Cancer Research Center
12:05 PM
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