Page 184 - ASHG 2012 Annual Meeting Program Guide

POSTER SESSIONS
173
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
1551
T JBASE: A Bayesian mixture model for joint
analysis of sub-phenotypes and epistasis.
R. Colak, T.
Kim, H. Kazan, P. M. Kim, A. Goldenberg.
1552
F IMProve: An R package for parallelizing 1000
Genomes based genotype imputation, statistical
analyses, and extraction of independent hit loci.
T. A.
Johnson, Y. Nakamura, M. Kubo, T. Tsunoda.
1553
W An automatic toolbox for genome-wide
association analyses.
J. Luan, S. J. Sharp, N. J.
Wareham, J. H. Zhao.
1554
T Variant association tool: A pipeline to perform
quality control and association analysis of sequence
and exome chip data.
G. Wang, B. Peng, S. M. Leal.
1555
F MaCH-Admix: Genotype imputation for admixed
populations.
E. Y. Liu, M. Li, W. Wang, Y. Li.
1556
W Two roads both taken: Walking the phenotypic
and genotypic paths to disease gene implication.
A.
Javed, P. Ng.
1557
T Inferring highly polymorphic gene alleles using
sequence data and SNP genotypes in the Han Chinese
population.
S. Chang, C. Fann, A. Hsieh, C. Shiu.
1558
F The design of custom-made genotyping arrays
to study asthma in populations of African descent.
J. Gao, Y. Hu, J. S. Lee, N. Pearson, G. Abecasis, I.
Ruczinski, T. H. Beaty, Z. Qin, R. A. Mathias, K. C. Barnes.
1559
W Detecting rare variants for both quantitative
and qualitative traits using pedigree data.
W. Guo, Y. Y.
Shugart.
1560
T IsoDOT detects differential RNA-isoform usage
between two or more samples with high sensitivity and
specificity.
W. Sun.
1561
F Identification of loss of heterozygosity from
unpaired tumor samples using next-generation
sequencing.
J. Lee, N. Pearson.
1562
W A robust and well-defined method for single
nucleotide variant and indel detection.
N. Tuzov.
1563
T DETECTANCE: Graphical software for study
design and planning, based on evaluation of the
detectance distributions for probands conditional on
the phenotypes of relatives.
T. Hiekkalinna, P. Norrgrann,
J. H. Lee, K. M. Weiss, M. Perola, J. D. Terwilliger.
1564
F Genetic instrumental variable studies of the
effects of maternal risk factors on oral clefts.
G. L.
Wehby, L. M. Moreno, P. Romitti, K. Christensen, L.
DeRoo, A. Wilcox, R. Munger, R. Lie, J. C. Murray.
1565
W The prevalence of X-linked hypohidrotic
ectodermal dysplasia in Denmark.
M. Nguyen-Nielsen,
S. Skovbo, D. Svaneby, L. Pedersen, J. Fryzek.
1566
T The PhenX Toolkit: Standard measures facilitate
1536
T On association analysis of rare variants
under population-substructure: An approach for
the detection of subjects that can cause bias in the
analysis.
D. Qiao, M. Mattheisen, C. Lange.
1537
F Identity-by-descent analysis of sequence data.
S. M. Smith, S. R. Browning, B. L. Browning.
1538
W Robust similarity regression for population
substructure in rare variant aggregation analyses.
J.
Tzeng, C. Smith.
1539
T Detecting differential expression in splice
variants in the absence of annotated isoforms using
RNAseq.
N. J. I. Lewin-Koh, T. Bhangale, M. Huntley, J.
Kaminker, F. Cai, M. van der Brug.
1540
F Identification of new genetics variants for T2D in
WTCCC data using genome-wide interaction analysis
followed by core SNP and gene determination.
Z.-X.
Zhu, Z.-H. Zhu, X. Tong, M. Liang, W.-C. Cui, M. Yang, L.
Zhou, M. D. Li, J. Zhu.
1541
W Imputing genotypes in large pedigrees: A
comparison between GIGI and BEAGLE.
C. Y. K.
Cheung, E. Wijsman.
1542
T A hidden Markov model for coalescent-based
mapping of complex trait loci from sequencing data in
large-scale case-control studies.
Z. Geng, P. Scheet, S.
Zoellner.
1543
F Genetic Simulation Resources: A website for the
registration and discovery of genetic data simulators.
B. Peng, B. Racine, H. Chen, L. Mechanic, L. Clarke, E.
Gillanders, E. Feuer.
1544
W Rare-variant tests in stratified populations.
M.
Schmidt, D. Kinnamon, E. Martin.
1545
T Software pipeline to detect SNPs and call their
genotypes.
M. Trost, H. M. Kang, G. Jun, G. R. Abecasis.
1546
F Bidimensional scale analysis: A novel approach
to genographic analysis.
Q. Huang, Y. Wu, Z. Li, X. Liu,
W. Xie.
1547
W Genotype probability distributions on complex
pedigrees, with applications to relationship testing.
M.
Vigeland, T. Egeland.
1548
T Trait specific genetic relatedness matrices for
heritability estimates using linear mixed models.
J.
Mefford, J. Witte.
1549
F The confounding effect of cryptic relatedness
on cohort studies for environmental risks.
K. Shibata,
G. Tamiya, M. Ueki, T. Nakamura, H. Narimatsu, I. Kubota,
Y. Ueno, T. Kato, H. Yamashita, A. Fukao, T. Kayama,
Yamagata University Genomic Cohort Consortium.
1550
W Genome wide mutation-rate map for the analysis
of recurrent de novo mutations.
P. Polak, S. R. Sunyaev.