An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 8254 | 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 | 901 | 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 | 201 | 2014 |
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 | 144 | 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 |
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 |
Software Tools for 2D Cell Segmentation P Liu, J Li, J Chang, P Hu, Y Sun, Y Jiang, F Zhang, H Shao Cells 13 (4), 352, 2024 | 1 | 2024 |
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. S Catreux, V Jain, L Murray, R Mehio, G Parnaby, C Roddey, M Ruehle, ... 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 |