PharmVIP: A Web-Based Tool for Pharmacogenomic Variant Analysis and Interpretation

The increasing availability of next generation sequencing (NGS) for personal genomics could promote pharmacogenomics (PGx) discovery and application. However, current tools for analysis and interpretation of pharmacogenomic variants from NGS data are inadequate, as none offer comprehensive analytic...

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Autores principales: Jittima Piriyapongsa, Chanathip Sukritha, Pavita Kaewprommal, Chalermpong Intarat, Kwankom Triparn, Krittin Phornsiricharoenphant, Chadapohn Chaosrikul, Philip J. Shaw, Wasun Chantratita, Surakameth Mahasirimongkol, Sissades Tongsima
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:12229e615c8b45a3a02129a35f5ed4672021-11-25T18:08:11ZPharmVIP: A Web-Based Tool for Pharmacogenomic Variant Analysis and Interpretation10.3390/jpm111112302075-4426https://doaj.org/article/12229e615c8b45a3a02129a35f5ed4672021-11-01T00:00:00Zhttps://www.mdpi.com/2075-4426/11/11/1230https://doaj.org/toc/2075-4426The increasing availability of next generation sequencing (NGS) for personal genomics could promote pharmacogenomics (PGx) discovery and application. However, current tools for analysis and interpretation of pharmacogenomic variants from NGS data are inadequate, as none offer comprehensive analytic functions in a simple, web-based platform. In addition, no tools exist to analyze human leukocyte antigen (HLA) genes for determining potential risks of immune-mediated adverse drug reaction (IM-ADR). We describe PharmVIP, a web-based PGx tool, for one-stop comprehensive analysis and interpretation of genome-wide variants obtained from NGS platforms. PharmVIP comprises three main interpretation modules covering analyses of pharmacogenes involved in pharmacokinetics, pharmacodynamics and IM-ADR. The Guideline module provides Clinical Pharmacogenetics Implementation Consortium (CPIC) drug guideline recommendations based on the translation of genotypic data in genes having guidelines. The HLA module reports HLA genotypes, potential adverse drug reactions, and the relevant drug guidelines. The Pharmacogenes module is employed for prioritizing variants according to variant effect on gene function. Detailed, customizable reports are provided as exportable files and as an interactive web version. PharmVIP is a new integrated NGS workflow for the PGx community to facilitate discovery and clinical application.Jittima PiriyapongsaChanathip SukrithaPavita KaewprommalChalermpong IntaratKwankom TriparnKrittin PhornsiricharoenphantChadapohn ChaosrikulPhilip J. ShawWasun ChantratitaSurakameth MahasirimongkolSissades TongsimaMDPI AGarticlepharmacogenomicsvariant analysisweb-based-toolnext-generation sequencingallele predictionCPIC dosing recommendationMedicineRENJournal of Personalized Medicine, Vol 11, Iss 1230, p 1230 (2021)
institution DOAJ
collection DOAJ
language EN
topic pharmacogenomics
variant analysis
web-based-tool
next-generation sequencing
allele prediction
CPIC dosing recommendation
Medicine
R
spellingShingle pharmacogenomics
variant analysis
web-based-tool
next-generation sequencing
allele prediction
CPIC dosing recommendation
Medicine
R
Jittima Piriyapongsa
Chanathip Sukritha
Pavita Kaewprommal
Chalermpong Intarat
Kwankom Triparn
Krittin Phornsiricharoenphant
Chadapohn Chaosrikul
Philip J. Shaw
Wasun Chantratita
Surakameth Mahasirimongkol
Sissades Tongsima
PharmVIP: A Web-Based Tool for Pharmacogenomic Variant Analysis and Interpretation
description The increasing availability of next generation sequencing (NGS) for personal genomics could promote pharmacogenomics (PGx) discovery and application. However, current tools for analysis and interpretation of pharmacogenomic variants from NGS data are inadequate, as none offer comprehensive analytic functions in a simple, web-based platform. In addition, no tools exist to analyze human leukocyte antigen (HLA) genes for determining potential risks of immune-mediated adverse drug reaction (IM-ADR). We describe PharmVIP, a web-based PGx tool, for one-stop comprehensive analysis and interpretation of genome-wide variants obtained from NGS platforms. PharmVIP comprises three main interpretation modules covering analyses of pharmacogenes involved in pharmacokinetics, pharmacodynamics and IM-ADR. The Guideline module provides Clinical Pharmacogenetics Implementation Consortium (CPIC) drug guideline recommendations based on the translation of genotypic data in genes having guidelines. The HLA module reports HLA genotypes, potential adverse drug reactions, and the relevant drug guidelines. The Pharmacogenes module is employed for prioritizing variants according to variant effect on gene function. Detailed, customizable reports are provided as exportable files and as an interactive web version. PharmVIP is a new integrated NGS workflow for the PGx community to facilitate discovery and clinical application.
format article
author Jittima Piriyapongsa
Chanathip Sukritha
Pavita Kaewprommal
Chalermpong Intarat
Kwankom Triparn
Krittin Phornsiricharoenphant
Chadapohn Chaosrikul
Philip J. Shaw
Wasun Chantratita
Surakameth Mahasirimongkol
Sissades Tongsima
author_facet Jittima Piriyapongsa
Chanathip Sukritha
Pavita Kaewprommal
Chalermpong Intarat
Kwankom Triparn
Krittin Phornsiricharoenphant
Chadapohn Chaosrikul
Philip J. Shaw
Wasun Chantratita
Surakameth Mahasirimongkol
Sissades Tongsima
author_sort Jittima Piriyapongsa
title PharmVIP: A Web-Based Tool for Pharmacogenomic Variant Analysis and Interpretation
title_short PharmVIP: A Web-Based Tool for Pharmacogenomic Variant Analysis and Interpretation
title_full PharmVIP: A Web-Based Tool for Pharmacogenomic Variant Analysis and Interpretation
title_fullStr PharmVIP: A Web-Based Tool for Pharmacogenomic Variant Analysis and Interpretation
title_full_unstemmed PharmVIP: A Web-Based Tool for Pharmacogenomic Variant Analysis and Interpretation
title_sort pharmvip: a web-based tool for pharmacogenomic variant analysis and interpretation
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/12229e615c8b45a3a02129a35f5ed467
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