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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
42862018
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
2162018
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
892014
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), 7, 2021
212021
How genome complexity can explain the difficulty of aligning reads to genomes
V Phan, S Gao, Q Tran, NS Vo
BMC bioinformatics 16, 1-15, 2015
132015
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, 61-75, 2021
122021
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
92019
RandAL: a randomized approach to aligning DNA sequences to reference genomes
NS Vo, Q Tran, N Niraula, V Phan
BMC genomics 15, 1-10, 2014
82014
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
82014
BRCA1/2 Mutations in Vietnamese Patients with Hereditary Breast and Ovarian Cancer Syndrome
TNN Le, VK Tran, TT Nguyen, NS Vo, TH Hoang, HL Vo, THT Nguyen, ...
Genes 13 (2), 268, 2022
72022
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
42016
A comprehensive evaluation of polygenic score and genotype imputation performances of human SNP arrays in diverse populations
DT Nguyen, TTH Tran, MH Tran, K Tran, D Pham, NT Duong, Q Nguyen, ...
Scientific reports 12 (1), 17556, 2022
32022
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
32021
Single-cell RNA sequencing data imputation using deep neural network
D Tran, FC Harris Jr, B Tran, NS Vo, H Nguyen, T Nguyen
ITNG 2021 18th International Conference on Information Technology-New …, 2021
32021
Leveraging known genomic variants to improve detection of variants, especially close-by Indels
NS Vo, V Phan
Bioinformatics 34 (17), 2918-2926, 2018
32018
A linear model for predicting performance of short-read aligners using genome complexity
Q Tran, S Gao, NS Vo, V Phan
BMC bioinformatics 16, 1-1, 2015
32015
Exploiting dependencies of pairwise comparison outcomes to predict patterns of gene response
NS Vo, V Phan
BMC bioinformatics 15, 1-13, 2014
32014
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
32013
Exploiting dependencies of patterns in gene expression analysis using pairwise comparisons
NS Vo, V Phan
Bioinformatics Research and Applications: 9th International Symposium, ISBRA …, 2013
32013
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Articles 1–20