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DMET(TM) 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 Polymorphis...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7362183/ https://www.ncbi.nlm.nih.gov/pubmed/32235355 http://dx.doi.org/10.3390/ht9020008 |
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author | Agapito, Giuseppe Settino, Marzia Scionti, Francesca Altomare, Emanuela Guzzi, Pietro Hiram Tassone, Pierfrancesco Tagliaferri, Pierosandro Cannataro, Mario Arbitrio, Mariamena Di Martino, Maria Teresa |
author_facet | Agapito, Giuseppe Settino, Marzia Scionti, Francesca Altomare, Emanuela Guzzi, Pietro Hiram Tassone, Pierfrancesco Tagliaferri, Pierosandro Cannataro, Mario Arbitrio, Mariamena Di Martino, Maria Teresa |
author_sort | Agapito, Giuseppe |
collection | PubMed |
description | 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. DMET(TM) 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 DMET(TM) 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® DMET(TM) Platform). |
format | Online Article Text |
id | pubmed-7362183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73621832020-07-21 DMET(TM) Genotyping: Tools for Biomarkers Discovery in the Era of Precision Medicine Agapito, Giuseppe Settino, Marzia Scionti, Francesca Altomare, Emanuela Guzzi, Pietro Hiram Tassone, Pierfrancesco Tagliaferri, Pierosandro Cannataro, Mario Arbitrio, Mariamena Di Martino, Maria Teresa High Throughput Review 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. DMET(TM) 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 DMET(TM) 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® DMET(TM) Platform). MDPI 2020-03-29 /pmc/articles/PMC7362183/ /pubmed/32235355 http://dx.doi.org/10.3390/ht9020008 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Agapito, Giuseppe Settino, Marzia Scionti, Francesca Altomare, Emanuela Guzzi, Pietro Hiram Tassone, Pierfrancesco Tagliaferri, Pierosandro Cannataro, Mario Arbitrio, Mariamena Di Martino, Maria Teresa DMET(TM) Genotyping: Tools for Biomarkers Discovery in the Era of Precision Medicine |
title | DMET(TM) Genotyping: Tools for Biomarkers Discovery in the Era of Precision Medicine |
title_full | DMET(TM) Genotyping: Tools for Biomarkers Discovery in the Era of Precision Medicine |
title_fullStr | DMET(TM) Genotyping: Tools for Biomarkers Discovery in the Era of Precision Medicine |
title_full_unstemmed | DMET(TM) Genotyping: Tools for Biomarkers Discovery in the Era of Precision Medicine |
title_short | DMET(TM) Genotyping: Tools for Biomarkers Discovery in the Era of Precision Medicine |
title_sort | dmet(tm) genotyping: tools for biomarkers discovery in the era of precision medicine |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7362183/ https://www.ncbi.nlm.nih.gov/pubmed/32235355 http://dx.doi.org/10.3390/ht9020008 |
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