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Bioinformatics (Oxford, England)|March 29, 2018
Leveraging known genomic variants to improve detection of variants, especially close-by IndelsNam S Vo, Vinhthuy PhanBMC Bioinformatics|October 29, 2014
Exploiting dependencies of pairwise comparison outcomes to predict patterns of gene responseNam S Vo, Vinhthuy PhanBMC Genomics|August 2, 2014
RandAL: a randomized approach to aligning DNA sequences to reference genomesNam S Vo, Quang Tran, Nobal Niraula, et al.BMC Bioinformatics|December 19, 2015
How genome complexity can explain the difficulty of aligning reads to genomesVinhthuy Phan, Shanshan Gao, Quang Tran, et al.Briefings in Bioinformatics|July 3, 2022
LmTag: functional-enrichment and imputation-aware tag SNP selection for population-specific genotyping arraysDat Thanh Nguyen, Quan Hoang Nguyen, Nguyen Thuy Duong, et al.Journal of Human Genetics|October 30, 2025
A comprehensive assessment of pharmacogenomic annotation tools for next-generation sequencing data: an emphasis on cyp2d6 and vietnamese genomic dataThien Khac Nguyen, Cuong Tri Pham, Tham Hoang, et al.Pharmacogenomics and Personalized Medicine|January 20, 2021
Review on Databases and Bioinformatic Approaches on Pharmacogenomics of Adverse Drug ReactionsHang Tong, Nga V T Phan, Thanh T Nguyen, et al.Scientific Reports|December 28, 2023
A rapid and reference-free imputation method for low-cost genotyping platformsVinh Chi Duong, Giang Minh Vu, Thien Khac Nguyen, et al.Scientific Reports|October 20, 2022
A comprehensive evaluation of polygenic score and genotype imputation performances of human SNP arrays in diverse populationsDat Thanh Nguyen, Trang T H Tran, Mai Hoang Tran, et al.Briefings in Bioinformatics|November 3, 2022
Assessing polygenic risk score models for applications in populations with under-represented genomics data: an example of VietnamDuy Pham, Buu Truong, Khai Tran, et al.Pageof 3