Please use this identifier to cite or link to this item:
https://www.um.edu.mt/library/oar/handle/123456789/99070
Title: | Personalized pharmacogenomics profiling using whole-genome sequencing |
Authors: | Mizzi, Clint Peters, Brock Mitropoulou, Christina Mitropoulos, Konstantinos Katsila, Theodora Agarwal, Misha R. Schaik, Ron H. N. van Drmanac, Radoje Borg, Joseph J. Patrinos, George P. |
Keywords: | Drugs -- Metabolism Genes -- Research Pharmacogenomics -- Research Genomes -- Analysis |
Issue Date: | 2014 |
Publisher: | Future Medicine Ltd. |
Citation: | Mizzi, C., Peters, B., Mitropoulou, C., Mitropoulos, K., Katsila, T., Agarwal, M. R., ... & Patrinos, G. P. (2014). Personalized pharmacogenomics profiling using whole-genome sequencing. Pharmacogenomics, 15(9), 1223-1234. |
Abstract: | Pharmacogenomics holds promise to rationalize drug use by minimizing drug toxicity and at the same time increase drug efficacy. There are currently several assays to screen for known pharmacogenomic biomarkers for the most commonly prescribed drugs. However, these genetic screening assays cannot account for other known or novel pharmacogenomic markers. We analyzed whole-genome sequences of 482 unrelated individuals of various ethnic backgrounds to obtain their personalized pharmacogenomics profiles. Bioinformatics analysis revealed 408,964 variants in 231 pharmacogenes, from which 26,807 were residing on exons and proximal regulatory sequences, whereas 16,487 were novel. analyses indicated that 1012 novel pharmacogene-related variants possibly abolish protein function. We have also performed whole-genome sequencing analysis in a seven-member family of Greek origin in an effort to explain the variable response rate to acenocoumarol treatment in two family members. Overall, our data demonstrate that whole-genome sequencing, unlike conventional genetic screening methods, is necessary to determine an individual's pharmacogenomics profile in a more comprehensive manner, which, combined with the gradually decreasing whole-genome sequencing costs, would expedite bringing personalized medicine closer to reality. |
URI: | https://www.um.edu.mt/library/oar/handle/123456789/99070 |
Appears in Collections: | Scholarly Works - FacHScABS |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
Personalized_pharmacogenomics_profiling_using_whole_genome_sequencing.pdf Restricted Access | 1.61 MB | Adobe PDF | View/Open Request a copy |
Items in OAR@UM are protected by copyright, with all rights reserved, unless otherwise indicated.