Brock A. Peters
Brock A. Peters
Senior Director, Research, Complete Genomics and MGI-Tech
E-mail megerősítve itt:
Hivatkozott rá
Hivatkozott rá
Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
R Drmanac, AB Sparks, MJ Callow, AL Halpern, NL Burns, BG Kermani, ...
Science 327 (5961), 78-81, 2010
Diverse somatic mutation patterns and pathway alterations in human cancers
Z Kan, BS Jaiswal, J Stinson, V Janakiraman, D Bhatt, HM Stern, P Yue, ...
Nature 466 (7308), 869-873, 2010
The PIK3CA gene is mutated with high frequency in human breast cancers
KE Bachman, P Argani, Y Samuels, N Silliman, J Ptak, S Szabo, ...
Cancer biology & therapy 3 (8), 772-775, 2004
Contribution of bone marrow–derived endothelial cells to human tumor vasculature
BA Peters, LA Diaz, K Polyak, L Meszler, K Romans, EC Guinan, JH Antin, ...
Nature medicine 11 (3), 261-262, 2005
Mutational analysis of the tyrosine phosphatome in colorectal cancers
Z Wang, D Shen, DW Parsons, A Bardelli, J Sager, S Szabo, J Ptak, ...
Science 304 (5674), 1164-1166, 2004
Oncogenic ERBB3 mutations in human cancers
BS Jaiswal, NM Kljavin, EW Stawiski, E Chan, C Parikh, S Durinck, ...
Cancer cell 23 (5), 603-617, 2013
Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells
BA Peters, BG Kermani, AB Sparks, O Alferov, P Hong, A Alexeev, Y Jiang, ...
Nature 487 (7406), 190-195, 2012
Somatic mutations in p85α promote tumorigenesis through class IA PI3K activation
BS Jaiswal, V Janakiraman, NM Kljavin, S Chaudhuri, HM Stern, W Wang, ...
Cancer cell 16 (6), 463-474, 2009
Genetic alterations and oncogenic pathways associated with breast cancer subtypes
X Hu, HM Stern, L Ge, C O'Brien, L Haydu, CD Honchell, PM Haverty, ...
Molecular cancer research 7 (4), 511-522, 2009
Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism
CP Schaaf, ML Gonzalez-Garay, F Xia, L Potocki, KW Gripp, B Zhang, ...
Nature genetics 45 (11), 1405-1408, 2013
A public resource facilitating clinical use of genomes
MP Ball, JV Thakuria, AW Zaranek, T Clegg, AM Rosenbaum, X Wu, ...
Proceedings of the National Academy of Sciences 109 (30), 11920-11927, 2012
Methods and compositions for long fragment read sequencing
R Drmanac, BA Peters, A Alexeev, P Hong
US Patent 8,592,150, 2013
Deep RNA sequencing analysis of readthrough gene fusions in human prostate adenocarcinoma and reference samples
S Nacu, W Yuan, Z Kan, D Bhatt, CS Rivers, J Stinson, BA Peters, ...
BMC medical genomics 4 (1), 1-22, 2011
Distinguishing cancer-associated missense mutations from common polymorphisms
JS Kaminker, Y Zhang, A Waugh, PM Haverty, B Peters, D Sebisanovic, ...
Cancer research 67 (2), 465-473, 2007
Multiple tagging of individual long DNA fragments
R Drmanac, BA Peters, A Alexeev
US Patent 9,328,382, 2016
Personalized pharmacogenomics profiling using whole-genome sequencing
C Mizzi, B Peters, C Mitropoulou, K Mitropoulos, T Katsila, MR Agarwal, ...
Pharmacogenomics 15 (9), 1223-1234, 2014
Processing and analysis of complex nucleic acid sequence data
R Drmanac, BA Peters, BG Kermani
US Patent 9,524,369, 2016
Sequencing Small Amounts of Complex Nucleic Acids
R Drmanac, BA Peters, BG Kermani
US Patent App. 13/448,279, 2014
Pharmacologic and Toxicologic Evaluation of C. novyi-NT Spores
LA Diaz Jr, I Cheong, CA Foss, X Zhang, BA Peters, N Agrawal, ...
Toxicological Sciences 88 (2), 562-575, 2005
Efficient and unique cobarcoding of second-generation sequencing reads from long DNA molecules enabling cost-effective and accurate sequencing, haplotyping, and de novo assembly
O Wang, R Chin, X Cheng, MKY Wu, Q Mao, J Tang, Y Sun, E Anderson, ...
Genome research 29 (5), 798-808, 2019
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