Page 262 - ASHG 2012 Annual Meeting Program Guide

POSTER SESSIONS
251
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
3399
W Deep-coverage whole genome sequencing of
100
Qatari reveals elevated prevalence of population-
specific variants linked to disease.
J. L. Rodriguez-
Flores, K. A. Fakhro, N. R. Hackett, J. Salit, J. Fuller, J. A.
Malek, R. Badii, A. Al-Marri, L. Chouchane, R. G. Crystal,
J. G. Mezey.
3400
T Single gene disorders in Western India: Cohort
of high risk group.
C. Ankleshwaria, J. Sheth, H. Patel, J.
Lekshami, F. Sheth.
3401
W Study on the distribution of rare genetic
variations in the French Canadian population.
S. Girard,
L.-P. Lemieux Perreault, I. Mongrain, G. Lettre, J. Rioux,
M. Phillips, S. de Denus, G. A. Rouleau, J.-C. Tardif, M.-P.
Dube.
3402
T Identification of a novel Native American Y
chromosome founding lineage in northwest South
America.
L. Roewer, M. Nothnagel, L. Gusmão, V. Gomes,
M. Gonzaléz, D. Corach, A. Sala, E. Alechine, T. Palha, N.
Santos, A. Ribeiro-dos-Santos, M. Geppert, S. Willuweit,
M. Nagy, S. Zweynert, M. Baeta, C. Núñez, B. Martínez-
Jarreta, F. González-Andrade, E. Fagundes de Carvalho,
D. Aparecida da Silva, J. J. Builes, D. Turbón, A. M. Lopez
Parra, E. Arroyo-Pardo, U. Toscanini, L. Borjas, C. Barletta,
S. Santos, M. Krawczak.
3403
W Single nucleotide variation analysis of protein
domain signatures of human genes.
J. Freudenberg.
3404
T Investigating the evolution of deleterious
mutations in the major histocompatibility complex
as a potential explanation for frequently observed
HLA-disease associations.
T. L. Lenz, D. M. Jordan, S.
R. Sunyaev.
3405
W Quantifying the degree of purifying selection
in genes associated with nephrotic syndrome.
M. G.
Sampson, M. Kretzler, H. M. Kang.
3406
T An assessment of population stratification
in rare variant association tests using an analytic
model of joint site frequency spectra.
M. Reppell, M.
Zawistowski, D. Wegmann, R. Weyant, P. L. St. Jean, M.
G. Ehm, M. R. Nelson, J. Novembre, S. Zöllner.
3407
W Estimating and interpreting
F
ST
:
The impact of
rare variants.
G. Bhatia, N. Patterson, S. Sankararaman,
A. L. Price.
3408
T Are rare and common variant stratification
patterns the same?
E. Génin, M.-C. Babron, M. de
Tayrac, D. N. Rutledge, E. Zeggini.
3409
W Variant frequency and the scale of population
structure.
P. Raska, O. De la Cruz Cabrera.
3410
T Male-specific common CNVs and complex
gender differences in CNV detected among 808
olfactory receptor loci, in 150 phenotypically normal
individuals from the 1000 Genome Project.
F.
Shadravan.
3386
W A scalable pipeline for local ancestry inference
using thousands of reference individuals.
C. B. Do, E.
Durand, J. M. Macpherson, B. Naughton, J. L. Mountain.
3387
T Global genome-wide variations comparisons
show a generally homogeneous Levant that has been
recently structured by culture.
M. Haber, D. Comas, P.
A. Zalloua.
3388
F Human and
Helicobacter pylori
ancestries
in Colombian populations with contrasting risks of
gastric cancer.
N. Kodaman, A. Pazos, M. B. Piazuelo, B.
G. Schneider, C. L. Shaffer, J. Romero-Gallo, T. de Sablet,
L. E. Bravo, K. Wilson, T. Cover, P. Correa, S. Williams.
3389
W Deep ancestry within a Neandertal-like region
on human chromosome 12.
F. L. Mendez, J. C. Watkins,
M. F. Hammer.
3390
T Sub-continental ancestry of admixed Caribbean
populations and implications for medical genomics
in the Americas.
A. Moreno Estrada, S. Gravel, M. L.
Cuccaro, F. Zakharia, P. Ortiz-Tello, R. J. Martinez, J. L.
McCauley, E. E. Kenny, D. J. Hedges, R. W. Morris, J. K.
Byrnes, S. Acevedo, P. J. Norman, Z. Layrisse, P. Parham,
C. D. Bustamante, E. R. Martin.
3391
W Population structure and ancestry inference
under sample selection bias.
S. S. Shringarpure, E. P. Xing.
3392
T Genome-wide effects of sex-specific
incompatibility on neutral introgression.
M. Uyenoyama.
3393
W Admixture analysis of spontaneous hepatitis
C virus clearance among individuals of African
descent.
G. L. Wojcik, P. Duggal on behalf of International
Consortium of HCV Spontaneous Resolution.
3394
T A genome-wide perspective of population
structure and individual admixture in Xinjiang:
Implications for demographic history and complex trait
gene mapping.
S. Xu, S. Li, D. Lu, P. Qin, H. Lou, W. Jin,
X. Pan, L. Jin.
3395
W Genomics variants in the endogamous Mashadi
Jewish population identified by pooled whole exome
sequencing.
H. Ostrer, W. J. Huh, G. Akler, L. U., M.
Popovic, D. Kural, J. Sheffield, E. Burns, G. Atzmon, C.
Oddoux.
3396
T An evaluation of genetic characteristics of two
population isolates from Greece: The HELIC-Pomak
and MANOLIS studies.
G. Dedoussis, I. Tachmazidou,
A. E. Farmaki, L. Southam, K. Palin, A. Kolb-Kokocinski,
W. Rayner, E. Daoutidou, I. Ntalla, K. Panoutsopoulou, E.
Tsafantakis, M. Karaleftheri, E. Zeggini.
3397
W Genomic variants in the Dominican population
identified by whole exome genotyping using Affymetrix
Axiom Arrays.
C. Oddoux, C. Cambell, L. U., H. Ostrer.
3398
T A population-based study and subsequent
disclosure of autosomal recessive disease-causing
mutations in a founder population.
J. X. Chong, R. L.
Anderson, R. Ouwenga, D. J. Waggoner, C. Ober.