User considerations in assessing pharmacogenomic tests and their clinical support tools

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User considerations in assessing pharmacogenomic tests and their clinical support tools

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scientific article published on 11 September 2018

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wetenschappelijk artikel

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наукова стаття, опублікована у 2018

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User considerations in assessing pharmacogenomic tests and their clinical support tools

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User considerations in assessing pharmacogenomic tests and their clinical support tools

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User considerations in assessing pharmacogenomic tests and their clinical support tools

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User considerations in assessing pharmacogenomic tests and their clinical support tools

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User considerations in assessing pharmacogenomic tests and their clinical support tools

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User considerations in assessing pharmacogenomic tests and their clinical support tools

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P1476

User considerations in assessing pharmacogenomic tests and their clinical support tools

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P2093

Andrea Huston

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Boyko Kabakchiev

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Gouri Mukerjee

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Ron van Schaik

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P2860

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering

The 1200 patients project: creating a new medical model system for clinical implementation of pharmacogenomics

Comparison of delivery strategies for pharmacogenetic testing services

Usability evaluation of pharmacogenomics clinical decision support aids and clinical knowledge resources in a computerized provider order entry system: a mixed methods approach.

SLCO1B1 variants and statin-induced myopathy--a genomewide study

Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset.

Shape-IT: new rapid and accurate algorithm for haplotype inference.

P2888

s41525-018-0065-4

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scholarly article

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10.1038/S41525-018-0065-4

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English

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P478

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Micheline Piquette-Miller

Ruslan Dorfman

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2018-09-11T00:00:00Z

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P698

30210808

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P921

pharmacogenomics

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6133969

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