Medizinische Universität Graz - Research portal

Logo MUG Resarch Portal

Selected Publication:

SHR Neuro Cancer Cardio Lipid Metab Microb

Enko, D; Michaelis, S; Schneider, C; Schaflinger, E; Baranyi, A; Schnedl, WJ; Muller, DJ.
The Use of Next-Generation Sequencing in Pharmacogenomics.
Clin Lab. 2023; 69(8): Doi: 10.7754/Clin.Lab.2023.230103
Web of Science PubMed FullText FullText_MUG

 

Leading authors Med Uni Graz
Enko Dietmar
Co-authors Med Uni Graz
Baranyi Andreas
Michaelis Simon
Schnedl Wolfgang
Schneider Christopher
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
BACKGROUND: Next-generation sequencing (NGS) methods have become more commonly performed in clinical and research laboratories. METHODS: This review summarizes the current laboratory NGS-based diagnostic approaches in pharmacogenomics including targeted multi-gene panel sequencing, whole-exome sequencing (WES), and whole-genome sequencing (WGS). RESULTS: Clinical laboratories perform multiple non-uniform types of pharmacogenetic panels, which can reduce the overall number of single-gene tests to be more cost-efficient. Compared to the targeted multi-gene panels, which are not typically designed to detect novel variants, WES and WGS have a greater potential to identify secondary pharmacogenomic findings, which might be predictive for the pharmacotherapy outcome of different patient settings. WGS overcomes the limitations of WES enabling a more accurate exome-sequencing at appropriate coverage and the sequencing of non-coding regions. Different NGS-based study designs with different test strategies and study populations, varying sample sizes, and distinct analytical and interpretation procedures lead to different identification results of pharmacogenomic variants. CONCLUSIONS: The rapid progress in gene sequencing technologies will overcome the clinical and laboratory challenges of WES and WGS. Further high throughput NGS-based pharmacogenomics studies in different populations and patient settings are necessary to expand knowledge about rare functional variants and to enhance translation in clinical practice.
Find related publications in this database (using NLM MeSH Indexing)
Humans - administration & dosage
Pharmacogenetics - administration & dosage
High-Throughput Nucleotide Sequencing - methods

Find related publications in this database (Keywords)
next-generation sequencing
pharmacogenomics
target-ed sequencing
whole-exome sequencing
whole-ge-nome sequencing
© Med Uni GrazImprint