Page 274 - ASHG 2012 Annual Meeting Program Guide

POSTER SESSIONS
263
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
3713
F Very high resolution HLA genotyping with the
454
Life Sciences GS FLX system: Simplification
of workflow using fusion primers or a four primer
system.
B. N. Hoglund, C. L. Holcomb, T. C. Williams, D.
Goodridge, H. A. Erlich.
3714
W Highly multiplexed amplicon preparation
for targeted re-sequencing of sample limited
specimens using the Ion AmpliSeq™ technology and
semiconductor sequencing.
C. Li, B. Kong, D. Joun, I.
Casuga, M. Shannon, S. Chen, M. Andersen, D. Ruff, R.
Bennett.
3715
F A fast solution to NGS library preparation with
low nanogram DNA input.
P. Liu, G. Lohman, E. Cantor,
B. W. Langhorst, E. Yigit, L. M. Apone, D. B. Munafo, C.
Sumner, F. J. Stewart, T. C. Evans, E. T. Dimalanta, T. B.
Davis.
3716
W Pre-capture pooling for targeted enrichment of
libraries for next-generation sequencing.
B. Marosy, B.
Craig, A. Robinson, M. Zilka, K. Hetrick, S. Griffith, H. Ling,
J. Romm, K. F. Doheny.
3717
F Rapid and accurate semiconductor-based
sequencing of human exomes: Workflow and
performance on a familial trio.
G. Meredith, G. Bee, L.
Pickle, M. Dudas, G. Del Mistro, C. Scafe, M. Schorn, J.
Miller, M. Minto, B. Reed, G. Fry, J. Gioia, J. Hildebrandt,
P. Leong, M. Reddy, K. Atehortua-Khalsa, M. Sedova, S.
McLaughlin, V. Sheth, M. Shah, D. Thomas, H. Breu, M.
Rhodes, C. Adams, F. Hyland, R. Bennett.
3718
W TotalScript: A versatile and robust tool for
RNAseq applications.
F. Syed, S. Kuersten, A. Radek, R.
Vaidyanathan.
3719
F Automating high-throughput creation
of sequencing libraries.
J. Bishop, W. Zhang, D.
Mandelman, M. Allen, A. Harris, R. Bennett.
3720
W Highest sample quality for molecular analysis
through ambient stabilization technologies: Improved
genome, transcriptome and proteome analysis from
saliva, blood and tissue samples.
R. Muller, V. Liberal, S.
Wilkinson, A. Stassinopoulos, J. Muller-Cohn.
3721
F Increased sensitivity in whole-genome bisulfite
sequencing: A novel ‘post-bisulfite conversion’ library
construction method for sub-nanogram inputs.
R.
Sooknanan, A. Adey, J. Hitchen, J. Shendure, N. Caruccio.
3722
W Highly efficient miRNA isolation method using
solid phase reverse immobilization technology and
Biomek automation.
B.-N. Lee.
3723
F miRNA extraction from human plasma using
high capacity miRNA anti-probe magnetic beads.
A.
Zampetaki, T. Xu, A. V. Vlassov, N. Bernard, M. Mayr.
3724
W Single Molecule Real-Time (SMRT
®
)
sequencing
of genes implicated in autosomal recessive diseases.
Y. Guo, A. Bashir, E. Gould, R. Kornreich, L. Edelmann,
T. Brandt, Y. Kasai, J. Chin, E. Paxinos, A. Kasarskis, E.
Schadt.
3700
W GnuBIO desktop sequencer: Fully integrated
DNA preparation sequencing and analysis.
T. Raz, A.
Aslam, J. Boyce, N. Nerkizian, J. Emhoff, A. Esmall, J.
Fanning, H. Ghandour, K. Moulton, P. Stokes, T. Hung, S.
Kiani, P. Mary, J. Healy.
3701
F Utilizing next-generation sequencing for exome
analysis.
K. Stangier, F. Ernst, Y. Kumar, T. Paprotka.
3702
W Novel enrichment reagent for the study of the
human microbiome.
F. J. Stewart, G. R. Feehery, E. Yigit,
E. T. Dimalanta, B. W. Langhorst, L. M. Apone, P. Liu, D.
B. Munafo, C. J. Sumner, J. Bybee, L. M. Mazzola, T. B.
Davis, S. Pradhan.
3703
F Structural variations identified using solid-state
nanodetectors.
J. Thompson, B. Bready, D. Dederich, D.
Hevroni, M. Jouzi, H.-Y. Lee, D. Lloyd, P. Mukhatira, M.
Nadel, J. Oliver, J. Saraidaridis.
3704
W Automaton of whole exome and targeted
sequencing workflows in a high-throughput lab.
M.
Zilka, B. Marosy, A. Robinson, J. Gearhart, B. Craig, J.
Romm, K. Doheny.
3705
F Automated genomic DNA QC ensures high
quality data from downstream workflows.
M.
Gassmann, D. Rabiller, A. Padmanaban, D. McDade-
Walker.
3706
W Optimization of a miRNA expression profiling
workflow for ion semiconductor sequencing.
T.
Guettouche, J. Clarke, A. Andersen, L. Navarro, Y.
Cardentey, W. Hulme, G. Bademci, D. Van Booven, D.
Hedges, M. Pericak-Vance, J. Gilbert.
3707
F Functionalized nanoparticles for effective DNA
purification.
A. Lai, A. Fu.
3708
W POP-ONE™: A new sieving matrix for
capillary electrophoresis that supports a wide range
of applications with a single instrument set-up.
J.
A. Romero, B. F. Johnson, F. Mercer, J. A. Fisher, D.
Rodriguez, S. Hung, M. Wenz, W. Liao, J. Lee.
3709
F Automation of the Agilent target enrichment
portfolio.
M. R. Visitacion, J. Karbowski, F. Roos, B. Arezi,
B. Novak, M. Isaksson, A. Giuffre, S. Happe, D. Roberts,
E. Leproust, F. Dahl.
3710
W Sequencing of complete HLA haplotypes:
Resequencing and population studies.
M. S. Won, S.
Norberg, T. Royce, T. Dunn, T. Mann, N. Nemat-Gorgani, L.
A. Guethlein, L. Abi-Rached, L. Tian, K. L. Gunderson, P. J.
Norman, M. Ronaghi, P. Parham.
3711
F DNA Sudoku: Hunting rare genetic variations
using combinatorial pooling.
D. Esposito, D. Golan, B.
Blumenstiel, Y. Erlich.
3712
W From sample collection to bacterial
identification in a single day: 16s rRNA sequencing
using novel primers on the Ion Torrent Personal
Genome Machine.
G. S. Watts, M. M. Oshiro, B. W.
Futscher, D. G. Armstrong.