Follow
Nam Sy Vo
Nam Sy Vo
Vingroup Big Data Institute
Verified email at vinbigdata.org - Homepage
Title
Cited by
Cited by
Year
The immune landscape of cancer
V Thorsson, DL Gibbs, SD Brown, D Wolf, DS Bortone, THO Yang, ...
Immunity 48 (4), 812-830. e14, 2018
25152018
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
1552018
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
742014
XML schema automatic matching solution
HQ Thang, VS Nam
International Journal of Electrical, Computer, and Systems Engineering 4 (1 …, 2010
392010
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
102021
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
102015
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
82019
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
72021
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
72014
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
72014
Leveraging known genomic variants to improve detection of variants, especially close-by Indels
NS Vo, V Phan
Bioinformatics 34 (17), 2918-2926, 2018
32018
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
32016
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
32015
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
22021
Improving variant calling by incorporating known genetic variants into read alignment
NS Vo, V Phan
BMC bioinformatics 16 (15), 1-1, 2015
22015
Exploiting dependencies of pairwise comparison outcomes to predict patterns of gene response
NS Vo, V Phan
BMC bioinformatics 15 (11), 1-13, 2014
22014
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
22013
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
22013
LmTag: functional-enrichment and imputation-aware tag SNP selection for population-specific genotyping arrays
DT Nguyen, Q Nguyen, DT Nguyen, NS Vo
bioRxiv, 2022
12022
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
12021
The system can't perform the operation now. Try again later.
Articles 1–20