Page 204 - ASHG 2013 Program Guide

POSTER SESSIONS
  191
POSTER SESSIONS
W=W
ednesday authors will present; T=Thursday authors will present; F=Friday authors will pr
esent
1917
T Accurate and rapid genetic analysis of genomic
data under mixed model with multiple variance
components.
H. M. Kang, S. Yang.
1918
F Detecting genetic heterogeneity in complex
diseases with a weighted U statistic.
Q. Lu, C. Wei, R.
C. Elston.
1919
W Efficient and accurate population-scale KIR
typing from SNP chip data.
S. Leslie, D. Vukcevic, J.
Traherne, S. Naess, M. Lathrop, T. H. Karlsen, M. Moffatt,
W. Cookson, J. Trowsdale, G. McVean, S. Sawcer.
1920
T PSEUDOMARKER 2.0: Efficient computation
of likelihoods using NOMAD.
A. Schaffer, E. M. Gertz,
T. Hiekkalinna, S. Le Digabel, C. Audet, J. D. Terwilliger.
1921
F MMAP: A comprehensive mixed model
program for analysis of pedigree and population data.
J. O’Connell.
1922
W SALAD: A software suite for admixture linkage
analysis and discovery.
R. Johnson, G. Nelson, C.
Winkler.
1923
T Local ancestry inference for whole genome
sequence data.
B. Maples, S. Gravel, E. Kenny, C.
Bustamante.
1924
F Estimating sample size and power for nested
cohort studies.
R. Hoffmann.
1925
W Impact of measurement error on testing genetic
association with quantitative traits.
J. Liao, X. Li, T. Y.
Wong, J. J. Wang, C. C. Khor, E. S. Tai, T. Aung, Y. Y. Teo,
C. Y. Cheng.
1926
T Slicing the genome: A new approach to
association in complex, longitudinal diseases.
A. Musolf,
D. Londono, A. Q. Nato, Jr., P. Vuistiner, C. A. Wise, L. Yu, S.
J. Finch, P. Bovet, M. Bochud, T. C. Matise, D. Gordon.
1927
F Use of electronic medical records to measure
phenotypic heritability.
S. Hebbring, Z. Ye, M. He, J.
Mayer, S. Schrodi, M. Brilliant.
1928
W Optimal strategies for identifying disease
associated singletons.
S. Rashkin, G. Jun, G. Abecasis.
1929
T Response dependent sampling designs and
analysis in studies with rare variants.
L. Sun, A.
Derkach, J. F. Lawless.
1930
F Quantitative-trait-dependent sampling designs
for genetic association analysis of a rare variant score.
Y. E. Yilmaz, J. F. Lawless, S. B. Bull.
1931
W Caveats of extreme sampling strategies for
resequencing studies.
H. Qin, W. Ouywang, S. Cao, T.
Yang, Y.-P. Wang, H.-W. Deng.
1932
T Identifying potential cancer vaccine targets with
high-throughput sequencing.
E. Aronesty, K. Robasky,
W. D. Jones.
1933
F A dynamic model for classification of gene
regulation with RNA-seq data.
L. Li, M. Xiong.
1900
F Pooled whole exome sequencing as a strategy
for establishing population mutation profiles
E. Rinella,
K. Upadhyay, C. Oddoux, H. Ostrer.
1901
W A hidden Markov random field app oach to
modeling genetic association based on graphs derived
from gene expression.
J. Lei, L. Liu, B. Devlin, K. Roeder.
1902
T A new statistical method for identifying
differentially methylated regions in complex diseases.
P. Liu, C. Chen, X. Hua, Y. Lu, M. Liang.
1903
F A nonparametric model for haplotypes in
population bottlenecks.
L. T. Elliott, Y. W. Teh.
1904
W Using network methodology to infer population
substructure.
D. Prokopenko, C. Lange, J. Hecker, P.
Costa, E. K. Silverman, H. Loehlein Fier.
1905
T eqtl-tools: A toolset for scalable eQTL mapping.
A. Di Narzo, K. Hao.
1906
F Trans-ethnic fine mapping of cis eQTLs ac oss
eight ancestry groups.
C. Grace, J. C. Whittaker, J.
Huxley-Jones, A. P. Morris.
1907
W Statistical methods for the analysis of gene
expression in single-family studies for genetic and
complex disease.
S. Merella, P. Brambilla, F. Martinelli
Bonesch, E. Stupka, P. Provero.
1908
T Probabilistic phase concordance for enhanced
detection of somatic allelic imbalance.
C. M. Hahn, S.
Vattathil, P. Scheet.
1909
F Conducting large-scale imputation studies on the
Cloud.
S. Buyske, K. Vahi, E. Deelman, U. Peters, T. C. Matise.
1910
W SKAT admix: Extending the SKAT method for
rare variant association to admixed populations.
A. E.
Byrnes, M. C. Wu, M. Li, Y. Li.
1911
T The visualization of probabilistic results from
consumer genetic testing for ethnicity at AncestryDNA.
R. E. Curtis, K. H. Freestone, M. J. Barber, J. M. Callaway,
K. Noto, Y. Wang, C. A. Ball, K. G. Chahine.
1912
F Next generation of genotype imputation
methods.
S. Das, G. R. Abecasis.
1913
W SECA: SNP Effect Concordance Analysis using
genome-wide association summary results.
D. Nyholt.
1914
T Testing Hardy-Weinberg equilibrium of multi-allelic
markers: Computational R code for implementing MCMC
algorithm via a Markov base.
M. Rao, S. Venkatesan.
1915
F Relative performance and application of
gene- and pathway-level methods for genome-wide
association studies.
G. L. Wojcik, W. H. Kao, P. Duggal.
1916
W Using GenTrain and zCall to identify problematic
SNPs in rare variant genotype calling.
J. Romm, I.
McMullen, M. Jewell, J. Zhang, E. Pugh, K. F. Doheny.