Prati
Fuli Yu
Naslov
Citirano
Citirano
Godina
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
14926*2015
A haplotype map of the human genome
hapmap
10602*2005
A map of human genome variation from population scale sequencing
DM Altshuler, ES Lander, L Ambrogio, T Bloom, K Cibulskis, TJ Fennell, ...
Nature 467 (7319), 1061-1073, 2010
8790*2010
An integrated map of genetic variation from 1,092 human genomes
1000G
Nature 491, 1, 2012
8300*2012
The international HapMap project
RA Gibbs, JW Belmont, P Hardenbol, TD Willis, FL Yu, HM Yang, ...
Nature Publishing Group, 2003
62212003
Integrating common and rare genetic variation in diverse human populations
International HapMap 3 Consortium
Nature 467 (7311), 52, 2010
31772010
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
23892015
Genome-wide detection and characterization of positive selection in human populations
PC Sabeti, P Varilly, B Fry, J Lohmueller, E Hostetter, C Cotsapas, X Xie, ...
Nature 449 (7164), 913-918, 2007
22242007
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
7092011
Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay
P Hardenbol, F Yu, J Belmont, J MacKenzie, C Bruckner, T Brundage, ...
Genome research 15 (2), 269-275, 2005
4902005
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini
Nature communications 5 (1), 3934, 2014
4402014
Integrative annotation of variants from 1092 humans: application to cancer genomics
E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ...
Science 342 (6154), 1235587, 2013
4222013
A genomewide admixture map for Latino populations
AL Price, N Patterson, F Yu, DR Cox, A Waliszewska, GJ McDonald, ...
The American Journal of Human Genetics 80 (6), 1024-1036, 2007
3432007
The 1000 Genomes Project: data management and community access
L Clarke, X Zheng-Bradley, R Smith, E Kulesha, C Xiao, I Toneva, ...
Nature methods 9 (5), 459-462, 2012
3422012
An integrative variant analysis suite for whole exome next-generation sequencing data
D Challis, J Yu, US Evani, AR Jackson, S Paithankar, C Coarfa, ...
BMC bioinformatics 13, 1-12, 2012
3172012
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline
JG Reid, A Carroll, N Veeraraghavan, M Dahdouli, A Sundquist, A English, ...
BMC bioinformatics 15, 1-11, 2014
2502014
The functional spectrum of low-frequency coding variation
GT Marth, F Yu, AR Indap, K Garimella, S Gravel, WF Leong, ...
Genome biology 12, 1-17, 2011
2422011
A SNP discovery method to assess variant allele probability from next-generation resequencing data
Y Shen, Z Wan, C Coarfa, R Drabek, L Chen, EA Ostrowski, Y Liu, ...
Genome research 20 (2), 273-280, 2010
2292010
Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes
D Liang, DS Cram, HU Tan, S Linpeng, Y Liu, H Sun, Y Zhang, F Tian, ...
Genetics in Medicine 21 (9), 1998-2006, 2019
2062019
Whole-genome sequence–based analysis of high-density lipoprotein cholesterol
Nature genetics 45 (8), 899-901, 2013
1462013
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