Page 269 - ASHG 2012 Annual Meeting Program Guide

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POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
3579
F Golden Helix GenomeBrowse: Cloud-enabled
visual analytics of DNA and RNA-seq NGS data.
G.
Rudy, S. Gardner, M. Thiesen.
3580
W Informatics challenges on utilizing next-
generation sequencing to advance disease
understanding.
S. Saisanit, J. Hakenberg, Y. Li.
3581
F Integrated genome-phenome analysis.
M. M.
Segal, M. S. Williams, J. G. Gleeson.
3582
W Variation data services at NCBI: Archives, tools,
and curation for research and medicine.
S. Sherry,
K. Addess, V. Ananiev, C. Chen, D. Church, M. Feolo, J.
Garner, T. Heffron, D. Hoffman, M. Kholodov, A. Kitts, J.
Lee, J. Lopez, D. Maglott, R. Maiti, L. Phan, G. Riley, W.
Rubinstein, D. Rudnev, Y. Shao, E. Shekhtman, K. Sirotkin,
D. Slotta, R. Tully, R. Villamarin-Salomon, Q. Wang, M. H.
Ward, H. Zhang.
3583
F snpActs: A versatile web interface for
annotating and prioritizing SNV data sets.
B. Stade, D.
Ellinghaus, B. Petersen, M. Forster, A. Franke.
3584
W Games for gene annotation and phenotype
classification.
A. I. Su, S. Loguercio, C. Wu, B. M. Good.
3585
F HMM-Fisher: A hidden Markov model-based
method for identifying differential methylation.
S. Sun,
X. Yu.
3586
W Automated HGVS-recommended sequence
variant description.
P. Taschner, J. F. J. Laros, M.
Vermaat, J. T. den Dunnen.
3587
F RNAseq analysis using the pipeline graphical
workflow environment in neuropsychiatric disorders.
F. Torri, I. D. Dinov, A. Zamanyan, S. Hobel, P. Petrosyan,
Z. Liu, P. Eggert, I. Guella, J. Pierce, A. P. Clark, J. A.
Knowles, J. Ames, C. Kesselman, A. W. Toga, S. Potkin,
M. P. Vawter, F. Macciardi.
3588
W ENViz: A Cytoscape plugin for integrative
statistical analysis and visualization of multiple sample
matched data sets.
A. Tsalenko, A. Kuchinsky, R. Navon,
M. L. Creech, I. Steinfeld, Z. Yakhini.
3589
F Determining probability of rare variants: Design
implications for family-based sequencing studies.
W.
Wang, G. Peng.
3590
W Harvest: A web-based biomedical data
discovery and reporting application development
platform.
P. S. White, B. Ruth, M. J. Italia, J. Miller, J. W.
Pennington.
3591
F Pinpoint: A new algorithm to detect gene-gene
interactions in large-scale genome-wide association
studies.
D. Wong, S. Szymczak, J. E. Bailey-Wilson.
3592
W A unified analysis framework for detecting
genetic variations from next-generation sequencing
data.
C. Xiao, S. Sherry.
3564
W Exome sequencing of Mayo Clinic Biobank
samples for evaluation of quality and quantity of data.
S. Middha, S. K. McDonnell, Z. C. Fogarty, M. S. DeRycke,
K. J. Johnson, N. M. Lindor, D. J. Schaid, J. E. Olson, J. R.
Cerhan, S. N. Thibodeau.
3565
F Genome-wide association study on the world
fastest supercomputer, k computer.
K. Misawa, A.
Hasegawa, T. Tsunoda.
3566
W A bioinformatics approach for the identification
of developmental QTL candidate genes.
A. Q. Nato, B.
Li, F. Chen, J. H. Millonig, T. C. Matise.
3567
F Multivariate profiling approach to inference on
differential expression in RNA-seq data with small
sample size.
S. Oh, M. Kim, S. Song.
3568
W Challenges and approaches to computational
candidate gene prioritization using gene networks.
P.
Pavlidis, E. Mercier, J. Gillis.
3569
F BlueSNP: An R package for high-scalability
genome-wide association studies on compute
clusters.
R. J. Prill, H. Huang, S. Tata.
3570
W Fast and accurate identification of novel
sequences in de novo human genome assemblies using
NSIT.
B. Pupacdi, A. Javed, M. J. Zaki, M. Ruchirawat.
3571
F NGS for the masses: Empowering biologists to
improve bioinformatic productivity.
K. Qaadri.
3572
W Evaluation and visualization of functional
perturbations of pathways based on whole genome
variations.
H. Qin, Y. Y. Shugart.
3573
F Use of an ad hoc information system to support
data search at a genomics center.
H. Qiu, F. Mentch, E.
Frackelton, C. Kim, L. Hermannsson, H. Hakonarson.
3574
W Using biosignatures to stratify clinical
response: Evaluation of classification methods using
simulated gene expression signatures and real patient
cohorts.
P. Ravindran, C. Ooi, L. Kai, H. Zhong, A.
Belousov, H. Bitter.
3575
F Mitre: A tool for bulk updates of SNP identifiers.
N. W. Rayner, N. Robertson, M. I. McCarthy.
3576
W Genomic analysis from sequencer to bedside:
An integrated analysis pipeline for research and
clinical sequencing.
J. G. Reid, M. N. Bainbridge, F.
Yu, M. Dahdouli, D. Challis, P. Pham, D. P. Sexton, E.
Boerwinkle, R. A. Gibbs.
3577
F Human genome pattern mining framework for
complex diseases.
M. Riemenschneider, M. Stoll.
3578
W A tool for selecting endogenous control for
qRT-PCR using high throughput expression data.
C.
S. Rocha, C. V. Maurer-Morelli, I. Lopes-Cendes, F. M.
Artiguenave.