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Related Concept Videos

Dosage Regimen: Individualization01:24

Dosage Regimen: Individualization

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Individualization in dosing regimens is the customization of medication doses for individual patients. Its necessity arises from the goal of maximizing therapeutic benefits while minimizing risks. This approach is pivotal because human responses to drugs can vary widely; what is effective for one person may be inadequate or excessive for another. Interpatient (intersubject) variability refers to differences in drug responses between individuals, while intrapatient (intrasubject) variability...
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Analysis of population pharmacokinetic data involves studying the behavior of drugs within diverse populations to understand their pharmacokinetic parameters. Traditional pharmacokinetic methods typically involve collecting samples from a few individuals and estimating these parameters. While these methods are commonly used, they have limitations in capturing the variability in drug response among individuals or heterogeneous populations. Population pharmacokinetics is employed to address these...
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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
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Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
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Bioequivalence Data: Statistical Interpretation01:16

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Body:The statistical interpretation of bioequivalence data is a significant aspect of pharmaceutical research. Bioequivalence refers to the absence of any significant difference in the rate and extent to which the active ingredient in pharmaceutical products becomes available at the site of drug action when administered at the same molar dose under similar conditions. This helps determine if different drug products have similar absorption rates, ensuring their interchangeability.Statistical...
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Genetic variation is the diversity in DNA sequences found among individuals of the same species. This diversity is crucial for a species' survival because it helps organisms adapt to environmental changes. Genetic variation begins with fertilization, where an egg and sperm cell merge. Each of these cells carries 23 chromosomes, up to 46 in the fertilized egg. Chromosomes are long DNA strands that contain genes, the basic units of heredity.
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Updated: Dec 2, 2025

Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
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Variant Interpretation in Current Pharmacogenetic Testing.

Sally Luvsantseren1, Michelle Whirl-Carrillo2, Katrin Sangkuhl2

  • 1Department of Pharmacy, Stanford Health Care, Stanford, CA 94305, USA.

Journal of Personalized Medicine
|November 4, 2020
PubMed
Summary
This summary is machine-generated.

Commercial pharmacogenetic testing companies show significant variability in gene panels and variant screening. This leads to discordant phenotype reporting, causing patient distress and highlighting the need for industry-wide consensus.

Area of Science:

  • Pharmacogenomics
  • Clinical Genomics
  • Genetics

Background:

Keywords:
CPICnomenclaturepharmacogeneticspharmacogenomicsprecision medicinestandardization

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  • Numerous commercial companies offer pharmacogenetic testing with varying gene panels and variant screening capabilities.
  • These companies generate reports with phenotypic interpretations and gene-drug interactions using proprietary algorithms and curated data.
  • Discrepancies in reporting arise from the freedom companies have in selecting evidence for interpretation.