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Friday, October 14
4:15
PM
–6:15
PM
Concurrent Platform Session C (51-60)
SESSION 54 – Statistical Genetics III: Analysis of
Sequence Data
Room 517A, Level 5, Convention Center
Moderators:
Marie-Pierre Dube, Univ. of Montreal,
Canada; Goncalo Abecasis, Univ. of Michigan, USA
187
/4:15
Quantitative trait analysis in the NHLBI
exome sequencing project.
D. Y. Lin, D. Zeng, L.
Lange, P. Auer, C. Carlson, R. Jackson, K. North on
behalf of NHLBI Exome Sequencing Project.
188
/4:30
Whole genome sequencing of 1000
individuals in an isolated population.
C. Sidore, S.
Sanna, F. Busonero, W. Chen, H. M. Kang, C.
Fuchsberger, F. Reinier, R. Berutti, D. Hovelson, M. F.
Urru, M. Marcelli, R. Cusano, M. Oppo, A. Maschio, M.
Pitzalis, M. Zoledziewska, A. Angius, R. Nagaraja, M.
Uda, D. Schlessinger, C. Jones, F. Cucca, G. Abecasis.
189
/4:45
Likelihood-based deletion analysis in a
sample of sequenced Sardinian individuals.
S.
Rashkin, T. Blackwell, C. Sidore, S. Sanna, F.
Busonero, W. Chen, H. M. Kang, C. Fuchsberger, F.
Reinier, R. Berutti, F. Deidda, M. F. Urru, M. Marcelli, R.
Cusano, M. Oppo, A. Maschio, M. Pitzalis, M.
Zoledziewska, A. Angius, R. Nagaraja, M. Uda, D.
Schlessinger, C. Jones, F. Cucca, G. Abecasis.
190
/5:00
Sequencing and genotyping thousands of
European genomes and exomes to better
understand the genetic architecture of type 2
diabetes: The GoT2D Study.
H. M. Kang, K. Gaulton,
B. F. Voight, C. Fuchsberger, R. D. Pearson, J.
Maguire, T. Teslovich, Y. Chen, J. Flannick, L. J. Scott,
L. Moutsianas, R. Poplin, P. Chines, J. Perry, C.
Sidore, M. Rivas, T. Blackwell, I. Prokopenko, T.
Fennell, G. Jun, T. Frayling, N. Burtt, G. R. Abecasis, P.
Donnelly, L. Groop, M. Boehnke, M. McCarthy, D.
Altshuler on behalf of Genetics of Type-2 Diabetes
Consortium.
191
/5:15
A longevity reference genome generated
from the world’s oldest woman.
H. Holstege, D. Sie,
T. Harkins, C. Lee, T. Ross, S. McLaughlin, M. Shah,
B. Ylstra, G. Meijer, H. Meijers-Heijboer, P. Heutink, S.
Shaw Murray, M. Reinders, G. Holstege, E.
Sistermans, S. Levy.
192
/5:30
Joint variant calling and analysis across
>4,000 exomes of European and African American
ancestry.
G. Jun, H. M. Kang, M. Rieder, M. DePristo,
G. Abecasis on behalf of NHLBI Exome Sequencing
Project.
193
/5:45
SNVer: A statistical tool for variant calling
in analysis of pooled or individual next-generation
sequencing data.
Z. Wei, W. Wang, P. Hu, G. L. Lyon,
H. Hakonarson.
194
/6:00
Improvement of haplotype phasing using
next-generation sequence data.
F. Zakharia, J. Kidd,
S. Gravel, C. D. Bustamante.
Cameras and all other recording devices are
strictly prohibited
in all session rooms. Thank you for your cooperation
Friday, October 14
4:15
PM
–6:15
PM
Concurrent Platform Session C (51-60
SESSION 55 – Epigenetics
Room 520, Level 5, Convention Center
Moderators:
Janine LaSalle, Univ. of California, Davi
USA; Peng Jin, Emory Univ. Sch. of Med., USA
195
/4:15
The Roadmap Epigenomic Mapping
Consortium: A community human epigenomics
resource.
L. Chadwick, NIH Roadmap Epigenomic
Mapping Consortium.
196
/4:30
Dissecting the role of
NLRP7
in regulati
of imprinting in the trophoblast.
S. Wen, S.
Mahadevan, S. Otta, A. Balasa, H. Peng, I. Van den
Veyver.
197
/4:45
Aberrant methylation by mutations of D
methyltransferase 1 cause peripheral and central
axonal degeneration.
C. Klein, M. Botuyan, Y. Wu,
Ward, G. Nicholson, S. Hammans, K. Hojo, H.
Yamanishi, A. Karpf, S. James, D. Wallace, M. Simo
C. Lander, J. Cunningham, G. Smith, W. Litchy, B.
Boes, E. Atkinson, S. Middha, P. Dyck, J. Parisi, G.
Mer, D. Smith, J. Dyck.
198
/5:00
Factors playing a role in epigenetic
mutations in Beckwith-Wiedemann syndrome.
V.
Dagar, J. Mann, D. Amor, E. Algar.
199
/5:15
5-Hydroxymethylcytosine-mediated
epigenetic dynamics during neurodevelopment a
aging.
K. Szulwach, X. Li, Y. Li, C. X. Song, H. Wu,
Dai, H. Irier, M. Gearing, A. I. Levey, A. Vasanthaku
L. A. Godley, Q. Chang, C. He, P. Jin.
200
/5:30
Methylomic profiling across brain and
blood: Brain area-specific differentially methylate
regions, individual differences, and allele-specific
DNA methylation.
J. Mill, M. Davies, M. Volta, R.
Dobson, E. Meaburn, L. Schalkwyk.
201
/5:45
Stochastic choice of allelic expression i
neural progenitor cells.
A. R. Jeffries, L. Perfect, J.
Mill, N. J. Bray, J. Ledderose, J. Price.
202
/6:00
Age effects on DNA methylation pattern
in humans.
S. Horvath, Y. Zhang, K. R. van Eijk, E.
Strengman, R. S. Kahn, M. P. M. Boks, R. A. Ophoff