Follow
Fan Zhang
Fan Zhang
Department of Computational Medicine and Bioinformatics, University of Michigan
Verified email at umich.edu - Homepage
Title
Cited by
Cited by
Year
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
82282012
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Nature genetics 46 (3), 234-244, 2014
8942014
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
JS Kooner, D Saleheen, X Sim, J Sehmi, W Zhang, P Frossard, LF Been, ...
Nature genetics 43 (10), 984, 2011
5892011
Targeted gene correction minimally impacts whole-genome mutational load in human-disease-specific induced pluripotent stem cell clones
K Suzuki, C Yu, J Qu, M Li, X Yao, T Yuan, A Goebl, S Tang, R Ren, ...
Cell stem cell 15 (1), 31-36, 2014
2002014
Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly
Y Li, H Zheng, R Luo, H Wu, H Zhu, R Li, H Cao, B Wu, S Huang, H Shao, ...
Nature biotechnology 29 (8), 723-730, 2011
1442011
Discovery of biclonal origin and a novel oncogene SLC12A5 in colon cancer by single-cell sequencing
C Yu, J Yu, X Yao, WKK Wu, Y Lu, S Tang, X Li, L Bao, X Li, Y Hou, R Wu, ...
Cell research 24 (6), 701-712, 2014
1432014
Ancestry-agnostic estimation of DNA sample contamination from sequence reads
F Zhang, M Flickinger, SAG Taliun, GR Abecasis, LJ Scott, SA McCaroll, ...
Genome Research 30 (2), 185-194, 2020
63*2020
Integrative analysis of two cell lines derived from a non-small-lung cancer patient–A panomics approach
O Mayba, F Gnad, M Peyton, F Zhang, K Walter, P Du, MA Huntley, ...
Biocomputing 2014, 75-86, 2014
112014
YHap: a population model for probabilistic assignment of Y haplogroups from re-sequencing data
F Zhang, R Chen, D Liu, X Yao, G Li, Y Jin, C Yu, Y Li, LJM Coin
BMC bioinformatics 14 (1), 331, 2013
62013
FASTQuick: rapid and comprehensive quality assessment of raw sequence reads
F Zhang, HM Kang
GigaScience 10 (2), giab004, 2021
32021
Leveraging Genetic Variants for Rapid and Robust Upstream Analysis of Massive Sequence Data
F Zhang
22019
Reference-free multiplexed single-cell sequencing identifies genetic modifiers of the human immune response
GC Hartoularos, Y Si, F Zhang, P Kathail, DS Lee, A Ogorodnikov, Y Sun, ...
bioRxiv, 2023.05. 29.542756, 2023
2023
DRAGEN Sets New Standard for Data Accuracy in PrecisionFDA Benchmark Data. Optimizing Variant Calling Performance with Illumina Machine Learning and DRAGEN Graph.
FZ Severine Catreux, Varun Jain, Lisa Murray, Rami Mehio, Gavin Parnaby ...
https://www.illumina.com/science/genomics-research/articles/dragen-shines …, 2022
2022
Method for detecting copy number variations by genome sequencing fragments
HY Fan Zhang, Ruibang Luo, Na Li, Yingrui Li, Jun Wang, Jian Wang
WO Patent WO2014040206A1, 2014
2014
Method and system for detecting polymorphism locus of genome target region
FZ Yingrui Li, Chang Yu, Ruibang Luo
WO Patent WO2012027958A1, 2013
2013
The system can't perform the operation now. Try again later.
Articles 1–15