| An evaluation of copy number variation detection tools from whole‐exome sequencing data R Tan, Y Wang, SE Kleinstein, Y Liu, X Zhu, H Guo, Q Jiang, AS Allen, ... Human mutation 35 (7), 899-907, 2014 | 268 | 2014 |
| Long-read-based human genomic structural variation detection with cuteSV T Jiang, Y Liu, Y Jiang, J Li, Y Gao, Z Cui, Y Liu, B Liu, Y Wang Genome biology 21, 1-24, 2020 | 235 | 2020 |
| A Bayesian framework for de novo mutation calling in parents-offspring trios Q Wei, X Zhan, X Zhong, Y Liu, Y Han, W Chen, B Li Bioinformatics 31 (9), 1375-1381, 2015 | 106 | 2015 |
| A gradient-boosting approach for filtering de novo mutations in parent–offspring trios Y Liu, B Li, R Tan, X Zhu, Y Wang Bioinformatics 30 (13), 1830-1836, 2014 | 41 | 2014 |
| abPOA: an SIMD-based C library for fast partial order alignment using adaptive band Y Gao, Y Liu, Y Ma, B Liu, Y Wang, Y Xing Bioinformatics 37 (15), 2209-2211, 2021 | 38 | 2021 |
| A deep learning approach for filtering structural variants in short read sequencing data Y Liu, Y Huang, G Wang, Y Wang Briefings in bioinformatics 22 (4), bbaa370, 2021 | 34 | 2021 |
| A pipeline for RNA-seq based eQTL analysis with automated quality control procedures T Wang, Y Liu, J Ruan, X Dong, Y Wang, J Peng BMC bioinformatics 22, 1-18, 2021 | 30 | 2021 |
| InteGO2: a web tool for measuring and visualizing gene semantic similarities using Gene Ontology J Peng, H Li, Y Liu, L Juan, Q Jiang, Y Wang, J Chen BMC genomics 17, 553-560, 2016 | 30 | 2016 |
| Disease module identification based on representation learning of complex networks integrated from GWAS, eQTL summaries, and human interactome T Wang, Q Peng, B Liu, Y Liu, Y Wang Frontiers in Bioengineering and Biotechnology 8, 418, 2020 | 27 | 2020 |
| Enhancing discoveries of molecular QTL studies with small sample size using summary statistic imputation T Wang, Y Liu, Q Yin, J Geng, J Chen, X Yin, Y Wang, X Shang, C Tian, ... Briefings in bioinformatics 23 (1), bbab370, 2022 | 21 | 2022 |
| Joint detection of copy number variations in parent-offspring trios Y Liu, J Liu, J Lu, J Peng, L Juan, X Zhu, B Li, Y Wang Bioinformatics 32 (8), 1130-1137, 2016 | 19 | 2016 |
| eQTLMAPT: fast and accurate eQTL mediation analysis with efficient permutation testing approaches T Wang, Q Peng, B Liu, X Liu, Y Liu, J Peng, Y Wang Frontiers in Genetics 10, 1309, 2020 | 15 | 2020 |
| Enabling massive XML-based biological data management in HBase J Liu, Q Liu, L Zhang, S Su, Y Liu IEEE/ACM transactions on computational biology and bioinformatics 17 (6 …, 2019 | 13 | 2019 |
| The personal genome browser: visualizing functions of genetic variants L Juan, M Teng, T Zang, Y Hao, Z Wang, C Yan, Y Liu, J Li, T Zhang, ... Nucleic acids research 42 (W1), W192-W197, 2014 | 11 | 2014 |
| Using semantic association to extend and infer literature-oriented relativity between terms L Cheng, J Li, Y Hu, Y Jiang, Y Liu, Y Chu, Z Wang, Y Wang IEEE/ACM Transactions on Computational Biology and Bioinformatics 12 (6 …, 2015 | 6 | 2015 |
| Family genome browser: visualizing genomes with pedigree information L Juan, Y Liu, Y Wang, M Teng, T Zang, Y Wang Bioinformatics 31 (14), 2262-2268, 2015 | 5 | 2015 |
| Fast and accurate classification of meta-genomics long reads with deSAMBA G Li, Y Liu, D Li, B Liu, J Li, Y Hu, Y Wang Frontiers in Cell and Developmental Biology 9, 643645, 2021 | 3 | 2021 |
| Correction to: Enhancing discoveries of molecular QTL studies with small sample size using summary statistic imputation T Wang, Y Liu, Q Yin, J Geng, J Chen, X Yin, Y Wang, X Shang, C Tian, ... Briefings in bioinformatics 23 (3), bbac139, 2022 | 2 | 2022 |
| PocaCNV: a tool to detect copy number variants from population-scale genome sequencing data Z Zhang, Y Liu, G Li, Y Wang 2021 IEEE International Conference on Bioinformatics and Biomedicine (BIBM …, 2021 | 2 | 2021 |
| Erratum to: abPOA: an SIMD-based C library for fast partial order alignment using adaptive band Y Gao, Y Liu, Y Ma, B Liu, Y Wang, Y Xing Bioinformatics 37 (19), 3384-3384, 2021 | 2 | 2021 |
