Evidence map›Paper›PMID 23095502›Full record

ArticleBMC bioinformatics2012

Imputation reliability on DNA biallelic markers for drug metabolism studies.

Vladan Mijatovic, Ilaria Iacobucci, Marco Sazzini, Luciano Xumerle, Antonio Mori, Pier Franco Pignatti, Giovanni Martinelli, Giovanni Malerba

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Article in BMC bioinformatics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Vladan MijatovicDep, of Life and Reproductions Sciences, Sec, of Biology and Genetics - University of Verona, strada Le grazie 8, 37134 Verona, Italy.
Ilaria Iacobucci
Marco Sazzini
Luciano Xumerle
Antonio Mori
Pier Franco Pignatti
Giovanni Martinelli
Giovanni Malerba

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImputation is a statistical process used to predict genotypes of loci not directly assayed in a sample of individuals. Our goal is to measure the performance of imputation in predicting the genotype of the best known gene polymorphisms involved in drug metabolism using a common SNP array genotyping platform generally exploited in genome wide association studies.

methodsThirty-nine (39) individuals were genotyped with both Affymetrix Genome Wide Human SNP 6.0 (AFFY) and Affymetrix DMET Plus (DMET) platforms. AFFY and DMET contain nearly 900000 and 1931 markers respectively. We used a 1000 Genomes Pilot + HapMap 3 reference panel. Imputation was performed using the computer program Impute, version 2. SNPs contained in DMET, but not imputed, were analysed studying markers around their chromosome regions. The efficacy of the imputation was measured evaluating the number of successfully imputed SNPs (SSNPs).

resultsThe imputation predicted the genotypes of 654 SNPs not present in the AFFY array, but contained in the DMET array. Approximately 1000 SNPs were not annotated in the reference panel and therefore they could not be directly imputed. After testing three different imputed genotype calling threshold (IGCT), we observed that imputation performs at its best for IGCT value equal to 50%, with rate of SSNPs (MAF > 0.05) equal to 85%.

conclusionsMost of the genes involved in drug metabolism can be imputed with high efficacy using standard genome-wide genotyping platforms and imputing procedures.

Indexed as

Genome-Wide Association StudyPolymorphism, Single NucleotideEconomics, PharmaceuticalGenetic MarkersGenome, HumanHapMap ProjectHumansLeukemia, Myeloid, AcutePharmacogeneticsReproducibility of ResultsSoftwareStatistics as TopicGenetic Markers

Identifiers

PMID23095502
PMCPMC3439717

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