| The immune landscape of cancer V Thorsson, DL Gibbs, SD Brown, D Wolf, DS Bortone, THO Yang, ... Immunity 48 (4), 812-830. e14, 2018 | 2515 | 2018 |
| Systematic analysis of splice-site-creating mutations in cancer RG Jayasinghe, S Cao, Q Gao, MC Wendl, NS Vo, SM Reynolds, Y Zhao, ... Cell reports 23 (1), 270-281. e3, 2018 | 155 | 2018 |
| Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1 AJ Bleyer, S Kmoch, C Antignac, V Robins, K Kidd, JR Kelsoe, G Hladik, ... Clinical Journal of the American Society of Nephrology 9 (3), 527-535, 2014 | 74 | 2014 |
| XML schema automatic matching solution HQ Thang, VS Nam International Journal of Electrical, Computer, and Systems Engineering 4 (1 …, 2010 | 39 | 2010 |
| Prevalence of pharmacogenomic variants in 100 pharmacogenes among Southeast Asian populations under the collaboration of the Southeast Asian Pharmacogenomics Research Network … C Runcharoen, K Fukunaga, I Sensorn, N Iemwimangsa, S Klumsathian, ... Human genome variation 8 (1), 1-6, 2021 | 10 | 2021 |
| How genome complexity can explain the difficulty of aligning reads to genomes V Phan, S Gao, Q Tran, NS Vo BMC bioinformatics 16 (17), 1-15, 2015 | 10 | 2015 |
| Ria: a novel regression-based imputation approach for single-cell RNA sequencing B Tran, D Tran, H Nguyen, NS Vo, T Nguyen 2019 11th International Conference on Knowledge and Systems Engineering (KSE …, 2019 | 8 | 2019 |
| Review on databases and bioinformatic approaches on pharmacogenomics of adverse drug reactions H Tong, NVT Phan, TT Nguyen, DV Nguyen, NS Vo, L Le Pharmacogenomics and Personalized Medicine 14, 61, 2021 | 7 | 2021 |
| RandAL: a randomized approach to aligning DNA sequences to reference genomes NS Vo, Q Tran, N Niraula, V Phan BMC genomics 15 (5), 1-10, 2014 | 7 | 2014 |
| How genome complexity can explain the hardness of aligning reads to genomes V Phan, S Gao, Q Tran, NS Vo 2014 IEEE 4th International Conference on Computational Advances in Bio and …, 2014 | 7 | 2014 |
| Leveraging known genomic variants to improve detection of variants, especially close-by Indels NS Vo, V Phan Bioinformatics 34 (17), 2918-2926, 2018 | 3 | 2018 |
| Repeat complexity of genomes as a means to predict the performance of short-read aligners Q Tran, S Gao, NS Vo, V Phan Proceedings of the 8th International Conference on Bioinformatics and …, 2016 | 3 | 2016 |
| A linear model for predicting performance of short-read aligners using genome complexity Q Tran, S Gao, NS Vo, V Phan BMC bioinformatics 16 (15), 1-1, 2015 | 3 | 2015 |
| A comprehensive imputation-based evaluation of tag SNP selection strategies DT Nguyen, HQ Dinh, GM Vu, DT Nguyen, NS Vo 2021 13th International Conference on Knowledge and Systems Engineering (KSE …, 2021 | 2 | 2021 |
| Improving variant calling by incorporating known genetic variants into read alignment NS Vo, V Phan BMC bioinformatics 16 (15), 1-1, 2015 | 2 | 2015 |
| Exploiting dependencies of pairwise comparison outcomes to predict patterns of gene response NS Vo, V Phan BMC bioinformatics 15 (11), 1-13, 2014 | 2 | 2014 |
| A randomized algorithm for aligning DNA sequences to reference genomes NS Vo, Q Tran, N Niraula, V Phan 2013 IEEE 3rd International Conference on Computational Advances in Bio and …, 2013 | 2 | 2013 |
| Exploiting dependencies of patterns in gene expression analysis using pairwise comparisons NS Vo, V Phan International Symposium on Bioinformatics Research and Applications, 173-184, 2013 | 2 | 2013 |
| LmTag: functional-enrichment and imputation-aware tag SNP selection for population-specific genotyping arrays DT Nguyen, Q Nguyen, DT Nguyen, NS Vo bioRxiv, 2022 | 1 | 2022 |
| Single-cell RNA sequencing data imputation using deep neural network D Tran, FC Harris, B Tran, NS Vo, H Nguyen, T Nguyen ITNG 2021 18th International Conference on Information Technology-New …, 2021 | 1 | 2021 |
Vinhthuy PhanAssociate Professor of Computer Science, University of MemphisVerified email at memphis.edu
