Goo Jun
Citado por
Citado por
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68-74, 2015
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56-65, 2012
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
JA Tennessen, AW Bigham, TD O’Connor, W Fu, EE Kenny, S Gravel, ...
science 337 (6090), 64-69, 2012
An integrated map of structural variation in 2,504 human genomes
PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ...
Nature 526 (7571), 75-81, 2015
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants
W Fu, TD O’connor, G Jun, HM Kang, G Abecasis, SM Leal, S Gabriel, ...
Nature 493 (7431), 216-220, 2013
The genetic architecture of type 2 diabetes
C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ...
Nature 536 (7614), 41-47, 2016
Loss-of-function mutations in APOC3, triglycerides, and coronary disease
New England Journal of Medicine 371, 22-31, 2014
Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data
G Jun, M Flickinger, KN Hetrick, JM Romm, KF Doheny, GR Abecasis, ...
The American Journal of Human Genetics 91 (5), 839-848, 2012
Multi-platform discovery of haplotype-resolved structural variation in human genomes
MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ...
Nature communications 10 (1), 1-16, 2019
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ...
The American Journal of Human Genetics 94 (2), 233-245, 2014
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration
X Zhan, DE Larson, C Wang, DC Koboldt, YV Sergeev, RS Fulton, ...
Nature genetics 45 (11), 1375-1379, 2013
An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data
G Jun, MK Wing, GR Abecasis, HM Kang
Genome Research 25 (6), 918-925, 2015
Randomised clinical trial: faecal microbiota transplantation for recurrent Clostridum difficile infection – fresh, or frozen, or lyophilised microbiota from a small pool of …
ZD Jiang, NJ Ajami, JF Petrosino, G Jun, CL Hanis, M Shah, L Hochman, ...
Alimentary Pharmacology & Therapeutics 45 (7), 899-908, 2017
Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus
A Mahajan, X Sim, HJ Ng, A Manning, MA Rivas, HM Highland, AE Locke, ...
PLoS Genet 11 (1), e1004876, 2015
Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees
L Almasy, TD Dyer, JM Peralta, G Jun, AR Wood, C Fuchsberger, ...
BMC proceedings 8 (S1), S2, 2014
Non-crossover gene conversions show strong GC bias and unexpected clustering in humans
AL Williams, G Genovese, T Dyer, N Altemose, K Truax, G Jun, ...
Elife 4, e04637, 2015
Tracking and segmentation of highway vehicles in cluttered and crowded scenes
G Jun, JK Aggarwal, M Gokmen
2008 IEEE Workshop on Applications of Computer Vision, 1-6, 2008
An efficient active learning algorithm with knowledge transfer for hyperspectral data analysis
G Jun, J Ghosh
Geoscience and Remote Sensing Symposium, 2008. IGARSS 2008. IEEE …, 2008
Omics-squared: human genomic, transcriptomic and phenotypic data for Genetic Analysis Workshop 19
J Blangero, TM Teslovich, X Sim, MA Almeida, G Jun, TD Dyer, ...
BMC proceedings 10 (7), 71-77, 2016
Spatially adaptive classification of land cover with remote sensing data
G Jun, J Ghosh
IEEE Transactions on Geoscience and Remote Sensing 49 (7), 2662-2673, 2011
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Artigos 1–20