Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

PharmCAT: A Pharmacogenomics Clinical Annotation Tool.

Clinical pharmacology and therapeutics - 1 Jul 2018

Klein Teri E, Ritchie Marylyn D

Abstract excerpt

Implementation of genomic medicine into clinical care continues to increase in prevalence in medical centers worldwide. As defined by the National Human Genome Research Institute, "Genomic medicine is an emerging medical discipline that involves using genomic information about an individual as part of their clinical care.…" The genomic information utilized falls broadly into two categories: 1) highly penetrant...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Decision Support Systems, Clinical
Share to Genomics and Rare Diseases
Share to Genotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pharmaceutical studies and practices

Share to Pharmacogenetics

Share to Pharmacogenetics and Drug Metabolism

Share to Phenotype

Share to Precision Medicine

Source

Open in PubMed Open full text

Identifiers

PMID: 29194583
DOI: 10.1002/cpt.928
PMCID: PMC5984125

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

PharmCAT: A Pharmacogenomics Clinical Annotation Tool.PMID 29194583Read ↗

How to Run the Pharmacogenomics Clinical Annotation Tool (PharmCAT).Semantic proximity Read ↗

PGMD: a comprehensive manually curated pharmacogenomic database.Semantic proximity Read ↗

The PharmGKB: integration, aggregation, and annotation of pharmacogenomic data and knowledge.Semantic proximity Read ↗

Pharmacogene Variation Consortium: A Global Resource and Repository for Pharmacogene Variation.Semantic proximity Read ↗

Genetic databases in pharmacogenomics: the Frequency of Inherited Disorders Database (FINDbase).Semantic proximity Read ↗

Progress towards the integration of pharmacogenomics in practice.Semantic proximity Read ↗

PharmGKB: an integrated resource of pharmacogenomic data and knowledge.Semantic proximity Read ↗

Genetic databases and their potential in pharmacogenomics.Semantic proximity Read ↗

From pharmacogenomic knowledge acquisition to clinical applications: the PharmGKB as a clinical pharmacogenomic biomarker resource.Semantic proximity Read ↗

Whole genome sequencing in pharmacogenomicsSemantic proximity Read ↗

Integrating large-scale genotype and phenotype data.Semantic proximity Read ↗

Pharmacogenomics in the era of next generation sequencing – from byte to bedsideSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.