An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 8247 | 2012 |
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 | 897 | 2014 |
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 | 590 | 2011 |
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 | 200 | 2014 |
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 | 144 | 2011 |
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 | 143 | 2014 |
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 | 11 | 2014 |
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 | 6 | 2013 |
FASTQuick: rapid and comprehensive quality assessment of raw sequence reads F Zhang, HM Kang GigaScience 10 (2), giab004, 2021 | 3 | 2021 |
Leveraging Genetic Variants for Rapid and Robust Upstream Analysis of Massive Sequence Data F Zhang | 2 | 2019 |
Generating and implementing a structural variation graph genome F Zhang, S Truong US Patent US20230420082A1, 2023 | | 2023 |
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 |