This is the program for the 2010 Joint Statistical Meetings in Vancouver, British Columbia.

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Keyword Search Criteria: genomic returned 41 record(s)
Sunday, 08/01/2010
A Hidden Ising Model for ChIP-chip Data Analysis
Qianxing Mo, Memorial Sloan-Kettering Cancer Center; Faming Liang, Texas A&M University
2:05 PM

A Modified Approach in Statistical Significance for Genomewide Studies
Nusrat Jahan, James Madison University; Pradeep Singh, Southeast Missouri State University
3:05 PM

Monday, 08/02/2010
Cancer Marker Identification via Penalized Integrative Analysis
Shuangge Ma, Yale University


Statistical Considerations on Validating Microarray Platform in Clinical Development
Guang (Gary) Chen, Merck & Co., Inc.; Christopher Ramsborg, Merck & Co., Inc.; Yue Wang, Merck & Co., Inc.; Miho Kibukawa, Merck & Co., Inc.; Joel A. Klappenbach, Merck & Co., Inc.


Doing Better Than Average: Tailored Therapeutics in Drug Development
Stan Young, National Institute for Statistical Science; Stephen J. Ruberg, Eli Lilly and Company; Frank Rockhold, GlaxoSmithKline; Sue-Jane Wang, FDA; Stephen Senn, University of Glasgow
1:00 AM

Risk Predictions from Genomewide Association Data
Hongyu Zhao, Yale University; Jia Kang, Yale University; Ruiyan Luo, Yale University; Judy Cho, Yale University
8:35 AM

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

Discriminating Between Microbial Populations
Frederick A. Matsen, Fred Hutchinson Cancer Research Center ; Steven N. Evans, University of California, Berkeley
9:35 AM

Large-Margin, Single-Path Hierarchical Classification with a General Loss
Lingzhou Xue, University of Minnesota; Xiaotong Shen, University of Minnesota
9:55 AM

Joint Inference of Sparse Network and Genetic Association in Genetical Genomics Studies
Hongzhe Li, University of Pennsylvania
11:00 AM

A Case Study of Using a Genomic Assay to Predict the Benefit of Chemotherapy in Treating Breast Cancer: Testing, Prediction, and Study Planning
William E. Barlow, Cancer Research and Biostatistics (CRAB); Carl Yoshizawa, Genomic Health, Inc.
11:00 AM

Learning Regulatory Network from Multiple Genomics Array Data
Pei Wang, Fred Hutchinson Cancer Research Center; Jie Peng, University of California, Davis
11:25 AM

Statistical Analysis of Somatic Changes in Cancer Genomics
Giovanni Parmigiani, Harvard University
11:25 AM

A Stochastic Partitioning Method to Associate High-Dimensional Data Sets
Mahlet G. Tadesse, Georgetown University; Stefano Monni, Weill Cornell Medical College
11:35 AM

Some Statistical Issues in the Analysis of High-Throughput Sequencing Data
Margaret Taub, The Johns Hopkins University
2:05 PM

Modeling with Pairwise Comparisons
Jeffrey Leek, Johns Hopkins Bloomberg School of Public Health; Leslie Cope, The Johns Hopkins University; Donald Geman, The Johns Hopkins University; Giovanni Parmigiani, Harvard University
2:05 PM

Integration of Genomic Data to Infer the Genetic Architecture of Complex Phenotypes
Sayan Mukherjee, Duke University; Qing Xiong, Duke University; Terrence Furey, Duke University
2:30 PM

Semiparametric Bayesian Analysis of High-Throughput Array CGH Data
Subharup Guha, University of Missouri
2:35 PM

An Orthogonal Transformed Aggregation Statistic to Test Gene Regulation with Prespecified Gene Sets or Pathways
Shuyan (Sabrina) Wan, Merck Research Laboratories; Nanshi Sha, Columbia University; Peggy Wong, Merck Research Laboratories
2:50 PM

Overcoming the Winner's Curse to Identify Biomarkers with Clinical Relevance in Drug Development
Lei Shen, Eli Lilly and Company; Haoda Fu, Eli Lilly and Company
3:20 PM

Tuesday, 08/03/2010
A Decision-Theoretic Approach to Gene Set Analysis
Simina Maria Boca, Johns Hopkins Bloomberg School of Public Health; Hector Corrada Bravo, Johns Hopkins Bloomberg School of Public Health; Giovanni Parmigiani, Harvard University; Jeffrey Leek, Johns Hopkins Bloomberg School of Public Health


Likelihood-Based Evaluation of Normalization Methods
Sadhvi Khanna, The University of Arizona


An Efficient Method for Estimating Chromosome Copy Number of Variations and Its Theoretical Properties
Yue Selena Niu, The University of Arizona; Heping Zhang, Yale University
9:00 AM

Challenges in Predicting Risk of Women Diseases Using Genomic Data
Mariza De Andrade, Mayo Clinic
11:55 AM

Detection of Parent-of-Origin Effects for Quantitative Traits in Complete and Incomplete Nuclear Families with Multiple Children
Feng He, The University of Hong Kong; Wing Kam Fung, The University of Hong Kong; Yue-Qing Hu, Nanjing Medical University; Ji-Yuan Zhou, Southern Medical University
2:20 PM

Wednesday, 08/04/2010
Bayesian Methods in Genomics: Searching for Unity in Diverse Data Sources
Bhramar Mukherjee, University of Michigan; Debashis Ghosh, Pennsylvania State University


Genomics in the Pharmaceutical Industry: Where Is It Headed?
Dhammika Amaratunga, Johnson & Johnson; James Colaianne, Johnson & Johnson


Statistics, Technology, Epigenomics, and Our Future
Rebecca W. Doerge, Purdue University; Paul Auer, Purdue University
10:35 AM

Novel Signal Processing-Based Methods for the Detection of Copy Number Changes in Human DNA
Catherine Stamoulis, Harvard Medical School; Rebecca Betensky, Harvard School of Public Health
2:05 PM

A Homogenous Compound Poisson Change Point Model Approach for the Analysis of CNVs in Genomic Data
Jie Chen, University of Missouri-Kansas City; Ayten Yigiter, Hacettepe University; Hong-Wen Deng, University of Missouri-Kansas City
2:20 PM

Efficient Exploration of Multiple ChIP-seq and ChIP-chip Data Sets
Hongkai Ji, The Johns Hopkins University
2:35 PM

Clustering with Exclusion Zones: Genomic Applications
Mark Segal, University of California, San Francisco
3:05 PM

Critiquing Bioinformatics Resources When ID Mapping Is Needed to Integrate Genomic and Proteomic Studies
Roger Day, University of Pittsburgh; Kevin McDade, University of Pittsburgh; Uma Chandran, University of Pittsburgh; Alex Lisovich, University of Pittsburgh
3:20 PM

Thursday, 08/05/2010
Biomarkers in Clinical Trials in the Development of Biologics and Risk Assessment
Samir Lababidi, FDA
8:50 AM

A New Procedure to Identify Neighborhoods of Adjacent SNPs That Show a Specific Biologically Meaningful Pattern of Associations with Multiple Clinical Endpoints
Stan Pounds, St. Jude Children's Research Hospital
8:55 AM

Integrative Clustering of Multiple Genomic Data Types Using a Regularized Joint Latent Variable Model
Ronglai Shen, Memorial Sloan-Kettering Cancer Center; Adam B. Olshen, University of California, San Francisco; Sijian Wang, University of Wisconsin-Madison
9:00 AM

A Penalized Matrix Decomposition, with Applications to Sparse Principal Components and Canonical Correlation Analysis
Daniela Witten, Stanford University; Rob Tibshirani, Stanford University; Trevor Hastie, Stanford University
9:25 AM

P-Values or Prediction Errors: What Is the Name of the Game in Genomics?
Rafal Kustra, University of Toronto
9:35 AM

Bayesian Joint Modeling of Multiple Gene Networks and Diverse Genomic Data to Identify Target Genes of a Transcription Factor
Peng Wei, The University of Texas School of Public Health; Wei Pan, University of Minnesota
9:55 AM

A Robust Statistical Framework for eQTL Analysis
Mohamedou Sow, Samuel Lunenfeld Research Institute; Gilles Durrieu, University Bordeaux 1; Laurent Briollais, Samuel Lunenfeld Research Institute
10:50 AM

Moments of Strings of DNA Bases
Robert J. Blodgett, FDA; Errol Strain, FDA
11:50 AM




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