Page 270 - ASHG 2012 Annual Meeting Program Guide

POSTER SESSIONS
259
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
3608
W DWAC-seq: Dynamic Window Approach for
CNV detection using next-generation targeted and full
genome sequencing tag density.
V. Koval, J. van Rooij,
K. Estrada, P. Arp, M. Jhamai, R. Kraaij, A. Uitterlinden, E.
Cuppen, V. Guryev.
3609
F Fast detection of de novo copy number variants
from case-parent SNP arrays identifies a deletion on
chromosome 7p14.1 associated with non-syndromic
isolated cleft lip/palate.
I. Ruczinski, R. B. Scharpf, S.
Younkin, H. Schwender, M. Marazita, A. F. Scott, T. H.
Beaty.
3610
W VarioML framework for comprehensive
variation data representation and exchange.
M. Byrne,
I. A. C. Fokkema, O. Lancaster, T. Adamusiak, A. Ahonen-
Bishopp, D. Atlan, C. Beroud, M. Cornell, R. Dalgeish, A.
Devereau, G. P. Patrinos, M. A. Swertz, P. E. M. Taschner,
G. A. Thorisson, M. Vihinen, A. J. Brookes, J. Muilu.
3611
F Gene-centered viewing, storing and sharing of
exome/genome variant and phenotype data.
J. T. den
Dunnen, I. F. Fokkema, I. C. Lugtenburg, J. Hoogenboom,
Z. Tatum, G. C. P. Schaafsma, M. Vermaat, J. F. J. Laros, P.
E. M. Taschner.
3612
W Leveraging metadata for experimental
discovery at the ENCODE portal.
E. L. Hong, C. Sloan, V.
Malladi, K. Rosenbloom, G. Barber, G. Binkley, E. T. Chan,
R. Fang, B. C. Hitz, D. Karolchik, V. Kirkup, K. Learned,
J. Long, M. Maddren, M. Wong, A. Zweig, D. Haussler, J.
Kent, J. M. Cherry.
3613
F A Bayesian hierarchical generalized linear model
for identifying multiple interacting genes in family-
based case-control studies.
J. Li, N. Yi.
3614
W A national platform for clinical genetic analysis
of high-throughput sequencing data in Norway.
M.
C. Eike, H. LÊrum, T. Hughes, S. Bremer, S. Bergan, G.
Thomassen, M. Aanestad, T. Grünfeld, D. E. Undlien.
3615
F Haplotyping human genomes using whole-
genome sequence data.
V. Bansal.
3616
W Comparing protein prediction methods using
disease-causing missense variants.
P. Duggal, Y. Kim,
M. K. Tilley, M. M. Parker, A. Maroo, A. P. Klein.
3617
F Considerations for the processing and direct-to-
consumer return of exome sequences.
E. D. Harrington,
C. McLean, A. Shmygelska, A. Chowdry, B. Naughton.
3618
W Topological mapping and exploration of
genotyping data using Iris.
J. Paquette, G. Singh, G.
Carlsson, P. Y. Lum.
3619
F Development of 1920 barcodes for large-scale
targeted sequencing using the Access Array™ system.
X. Wang, F. Kaper, P. Chen, C. Friedlnader, G. Sun, A. May.
3620
W NGS Catalog: A database of next-generation
genome sequencing studies in humans.
J. Xia, Q.
Wang, P. Jia, B. Wang, W. Pao, Z. Zhao.
3593
F HMM-DM: Identifying differential methylation
patterns using a hidden Markov model.
X. Yu, S. Sun.
3594
W Genotype calling for next-generation
sequencing data from multiple populations.
K. Zhang,
D. Zhi.
3595
F Detecting structural variants in cancer from
whole genome and exome sequencing.
J. Zhang, Y. Shi,
W. Foulkes, J. Majewski.
3596
W Causal inference of gene regulation based on
sub-network assembly.
W. Hsieh, C. Peng, A. Dai, S.
Peng, T. Yen.
3597
F Identification of candidate variants in population
based whole exome sequencing data through
integration of functional prediction with bayesian
penalized regression.
J. Lu, A. Sabo, J. Reid, D. Muzny,
E. Boerwinkle, R. Gibbs, ARRA Autism Sequencing
Consortium.
3598
W Joint association of multiple correlated
phenotypes using matrix-variate linear mixed-models.
N. Furlotte, E. Eskin.
3599
F The human gene connectome: A map of short
cuts for morbid allele discovery.
Y. Itan, S. Y. Zhang,
G. Vogt, A. Abhyankar, L. Quintana-Murci, L. Abel, J. L.
Casanova.
3600
W Transcriptome sequencing of nPOD type
1
diabetes pancreatic samples for viral sequence
identification.
S. Morfopoulou, G. Zhao, R. Ferreira, A.
Pugliese, J. Petrosino, L. Thackray, V. Plagnol, nPOD-Virus
Group.
3601
F VARITAS: Variant analysis with rapid
incorporation of annotation sources.
B. Powell.
3602
W Clinical diagnostic tools for family genome and
exome data.
A. Russell, F. De La Vega, J. Rule, M. Reese.
3603
F ASAP: An easy-to-use pipeline for sequencing
data processing.
E. Torstenson, C. Li.
3604
W Identifying biological pathways and human
diseases in high-throughput human genetic studies.
C.
Xie, X. Mao, J. Huang, Y. Ding, J. Wu, S. Dong, L. Kong, G.
Gao, C. Li, L. Wei.
3605
F GenAMap: A visual analytics software platform
for eQTL and GWAS analysis.
E. Xing, R. Curtis, S. Lee,
S. Shringarpure, J. Yin.
3606
W PHV: A high accuracy SNP and indel variant
caller based on the profile hidden Markov model.
M.
Zhao, W. Lee, G. Marth.
3607
F Developing copy number variation based case-
control association analysis tool and its application for
disease analysis.
Y. Chung, J. H. Kim, H. J. Hu, S. H. Yim,
J. S. Bae, S. Y. Kim.