DMETTM基因分型:精准医学时代发现生物标志物的工具。

Q2 Biochemistry, Genetics and Molecular Biology
High-Throughput Pub Date : 2020-03-29 DOI:10.3390/ht9020008
Giuseppe Agapito, Marzia Settino, Francesca Scionti, Emanuela Altomare, Pietro Hiram Guzzi, Pierfrancesco Tassone, Pierosandro Tagliaferri, Mario Cannataro, Mariamena Arbitrio, Maria Teresa Di Martino
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引用次数: 9

摘要

了解参与药物代谢的基因的遗传变异可以减少药物不良反应,提高疗效,改善医疗保健结果和经济效益。许多高通量工具可用于已知与药物和外源代谢相关的单核苷酸多态性(snp)的基因分型。DMETTM平台是发现与常见和罕见疾病的疗效或毒性相关的生物标志物的snp面板的一个例子。由于DMETTM平台产生的大量信息难以分析,因此需要开发和实现用于统计和数据挖掘分析的算法和工具。这些软件可以有效地处理组学数据,以验证DMET测定确定的探索性snp,并将它们与药物疗效、毒性和/或癌症易感性联系起来。在这篇综述中,我们提出了一套用于预处理和分析dmet - snp数据的生物信息学框架。特别是,我们引入了一个使用基因组学查询语言的工作流程,这是一种专门为基因组学设计的高级查询语言,能够查询公共数据集(如ENCODE, TCGA, GENCODE注释数据集等),并将它们与私有数据集(例如,Affymetrix®DMETTM平台的输出)相结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

DMET<sup>TM</sup> Genotyping: Tools for Biomarkers Discovery in the Era of Precision Medicine.

DMET<sup>TM</sup> Genotyping: Tools for Biomarkers Discovery in the Era of Precision Medicine.

DMET<sup>TM</sup> Genotyping: Tools for Biomarkers Discovery in the Era of Precision Medicine.

DMETTM Genotyping: Tools for Biomarkers Discovery in the Era of Precision Medicine.

The knowledge of genetic variants in genes involved in drug metabolism may be translated into reduction of adverse drug reactions, increase of efficacy, healthcare outcomes improvement and economic benefits. Many high-throughput tools are available for the genotyping of Single Nucleotide Polymorphisms (SNPs) known to be related to drugs and xenobiotics metabolism. DMETTM platform represents an example of SNPs panel to discover biomarkers correlated to efficacy or toxicity in common and rare diseases. The difficulty in analyzing the mole of information generated by DMETTM platform led to the development and implementation of algorithms and tools for statistical and data mining analysis. These softwares allow efficient handling of the omics data to validate the explorative SNPs identified by DMET assay and to correlate them with drug efficacy, toxicity and/or cancer susceptibility. In this review we present a suite of bioinformatic frameworks for the preprocessing and analysis of DMET-SNPs data. In particular, we introduce a workflow that uses the GenoMetric Query Language, a high-level query language specifically designed for genomics, able to query public datasets (such as ENCODE, TCGA, GENCODE annotation dataset, etc.) as well as to combine them with private datasets (e.g., output from Affymetrix® DMETTM Platform).

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来源期刊
High-Throughput
High-Throughput Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
3.60
自引率
0.00%
发文量
0
审稿时长
9 weeks
期刊介绍: High-Throughput (formerly Microarrays, ISSN 2076-3905) is a multidisciplinary peer-reviewed scientific journal that provides an advanced forum for the publication of studies reporting high-dimensional approaches and developments in Life Sciences, Chemistry and related fields. Our aim is to encourage scientists to publish their experimental and theoretical results based on high-throughput techniques as well as computational and statistical tools for data analysis and interpretation. The full experimental or methodological details must be provided so that the results can be reproduced. There is no restriction on the length of the papers. High-Throughput invites submissions covering several topics, including, but not limited to: -Microarrays -DNA Sequencing -RNA Sequencing -Protein Identification and Quantification -Cell-based Approaches -Omics Technologies -Imaging -Bioinformatics -Computational Biology/Chemistry -Statistics -Integrative Omics -Drug Discovery and Development -Microfluidics -Lab-on-a-chip -Data Mining -Databases -Multiplex Assays
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