ABOUT ME
- E-mail: [email protected]
- Universityof Pennsylvania, Philadelphia -PhD in Molecular Biology/Genomics, 2013
- University of Science, Ho Chi Minh, Vietnam -B.S. in Biotechnology, 2004.
Tiến sĩ Giang Hoa là 1 trong 3 nhà đồng sáng lập Gene Solutions. Hiện, ông làm việc và nghiên cứu tại Viện Di truyền Y học- Gene Solutions, TP.HCM.
Trải qua gần 10 năm nghiên cứu và ứng dụng thực tiễn, TS Giang Hoa và cộng sự đã đóng góp tích cực để phát triển các xét nghiệm chẩn đoán và sàng lọc di truyền hiệu quả, toàn diện trong các lĩnh vực chăm sóc thai sản, chẩn đoán bệnh di truyền, tầm soát phát hiện và điều trị ung thư. TS Giang Hoa là tác giả và đồng tác giả của nhiều công trình nghiên cứu được công bố trong nước và quốc tế.
WORK EXPERIENCE
TIMELINE
2004
2004-2006
Research scientist
University of Medicine and Pharmacy, Ho Chi Minh city
Research scientist, Dept. of Histology, Embryology, and Genetics
- Establish mean values of alpha-fetoprotein (AFP), human chorionic gonadotropin (hCG), and unconjugated estriol (UE3) in Vietnamese population for screening fetal aneuploidies.
2008-2009
Teaching assistant
University of Pennsylvania
Teaching assistant, Molecular Biology
- Lecturer for a Microbiology laboratory.
2006-2013
PhD student
University of Pennsylvania
PhD student, Molecular Biology/Genomics
- Effects of temperature on global gene expression in natural strains of budding yeast
2013
2013-2015
Postdoctoral fellow
University of Pennsylvania
Postdoctoral fellow, Laboratory of Junhyong Kim
- Develop a new sequencing method for whole genome sequencing of single cells, new species, and microbiomes using transposon tagging and in vitro transcription.
- Collaborate with a pharmacology lab to develop a method for single mitochondrial sequencing.
2017
2017-2021
Principle investigator
Medical Genetics Institute, Ho Chi Minh city, Vietnam
Principle investigator, Computational Biology Group
- Develop cost-effective genetic screening and diagnostic tests for hereditary diseases, cancer, and prenatal/postnatal disorders.
- Oversee the development of analytic methods and technologies using next- generation sequencing in medical genetics.
- Lead analytic efforts for various projects to evaluate risk of genetic diseases in Vietnamese population.
PUBLICATIONS
MOST RECENT
- Nguyen HN, Cao NT, ..Giang H, Tran LS(2021). Liquid biopsy uncovers distinct patterns of DNA methylation and copy number changes in NSCLC patients with different EGFR-TKI resistant mutations. Sci Rep.11, 16436.
- Tran NH, Nguyen Thi TH, .. Phan MD, Giang H (2021). Genetic landscape of recessive diseases in the Vietnamese population from large-scale clinical exome sequencing. Hum Mutat. 42:1229-1238
- TM Tong, TTH Dao, .. TC Tran, Giang H (2021). Genetic analysis of Vietnamese patients with early-onset Alzheimer's disease. Int J Neurosci. 21:1-8
- Tran, N.H., Vo, T.B., Nguyen, V.T.,.. Nguyen HN, Giang H and Phan MD (2020). Genetic profiling of Vietnamese population from large-scale genomic analysis of non-invasive prenatal testing data. Sci Rep. 10, 19142.
- Tran LS, Nguyen QTT,.., Phan MD, Nguyen HN and Giang H (2020). Ultra-Deep Massive Parallel Sequencing of Plasma Cell-Free DNA Enables Large-Scale Profiling of Driver Mutations in Vietnamese Patients With Advanced Non-Small Cell Lung Cancer. Front. Oncol. 10:1351.
- Dang AH, Tran V, Tran T,.., Nguyen HN, Tran LS and Giang H. Actionable Mutation Profiles of Non-Small Cell Lung Cancer patients from Vietnamese population. Sci Rep 10, 2707 (2020)
- Nguyen HT, Tran DH, Ngo QD,.., Tran LS, Giang H and Nguyen HN (2020). Evaluation of a Liquid Biopsy Protocol using Ultra-Deep Massive Parallel Sequencing for Detecting and Quantifying Circulation Tumor DNA in Colorectal Cancer Patients. Cancer investigation, 38 (2), 85–93.
- Tran LS, Pham HT, Tran VU,.., Giang H and Nguyen HN (2019). Ultra-deep massively parallel sequencing with unique molecular identifier tagging achieves comparable performance to droplet digital PCR for detection and quantification of circulating tumor DNA from lung cancer patients. (12), e0226193.
- Phan MD, Vo BT, Nguyen TV, Tran NT, Trinh HNT, Nguyen TTQ, Nguyen NH, Tran TT, Tran UV, Dao TTH, Pham AH, Tran TH, Truong KD, Hoang TTD, Do TT, Nguyen HN, Giang H (2019). Reducing false positive rate of fetal monosomy X in non-invasive prenatal testing using a combined algorithm to detect maternal mosaic monosomy X. Prenat Diagn. 2019; 39: 324-327.
- Morris J, Na YJ, Zhu H, Lee J-H, Giang H, Ulyanova AV, Baltuch GH, Brem S, Chen I, Kung DK, Lucas TH, O'Rourke DM, Wolf JA, Grady MS, Sul JY, Kim J, Eberwine J (2017) Pervasive within-Mitochondrion Single-Nucleotide Variant Heteroplasmy as Revealed by Single-Mitochondrion Sequencing. Cell Reports 21(10): p2706-2713.
- Phan M-D, Nguyen VT, Trinh NTH, Vo TB, Nguyen MT, Nguyen HN, Nguyen TQT, Do TTT, Hoang TDT, Truong DK, Giang H, Nguyen H-N (2018) Establishing and validating non-invasive prenatal testing procedure for fetal aneuploidies in a low-income setting. J Matern Fetal Neonatal Med. 2018 Jul 10:1-7.