Testing for bimodality in frequency distributions of data suggesting polymorphisms of drug metabolism--hypothesis testing
- PMID: 2611088
- PMCID: PMC1380036
- DOI: 10.1111/j.1365-2125.1989.tb03558.x
Testing for bimodality in frequency distributions of data suggesting polymorphisms of drug metabolism--hypothesis testing
Abstract
1. The theory of methods of hypothesis testing in relation to the detection of bimodality in density distributions is discussed. 2. Practical problems arising from these methods are outlined. 3. The power of three methods of hypothesis testing was compared using simulated data from bimodal distributions with varying separation between components. None of the methods could determine bimodality until the separation between components was 2 standard deviation units and could only do so reliably (greater than 90%) when the separation was as great as 4-6 standard deviation units. 4. The robustness of a parametric and a non-parametric method of hypothesis testing was compared using simulated unimodal distributions known to deviate markedly from normality. Both methods had a high frequency of falsely indicating bimodality with distributions where the components had markedly differing variances. 5. A further test of robustness using power transformation of data from a normal distribution showed that the algorithms could accurately determine unimodality only when the skew of the distribution was in the range 0-1.45.
Similar articles
-
Testing for bimodality in frequency distributions of data suggesting polymorphisms of drug metabolism--histograms and probit plots.Br J Clin Pharmacol. 1989 Dec;28(6):647-53. doi: 10.1111/j.1365-2125.1989.tb03557.x. Br J Clin Pharmacol. 1989. PMID: 2611087 Free PMC article.
-
Analysis of polymorphic variation in drug metabolism: I. Kernal density estimation.Clin Invest Med. 1994 Aug;17(4):281-9. Clin Invest Med. 1994. PMID: 7982291
-
Pharmacokinetic-pharmacogenetic modelling in the detection of polymorphisms in xenobiotic metabolism.Ann Occup Hyg. 1990 Dec;34(6):653-62. doi: 10.1093/annhyg/34.6.653. Ann Occup Hyg. 1990. PMID: 2291588 Review.
-
STAR_outliers: a python package that separates univariate outliers from non-normal distributions.BioData Min. 2023 Sep 4;16(1):25. doi: 10.1186/s13040-023-00342-0. BioData Min. 2023. PMID: 37667378 Free PMC article.
-
Genetic polymorphism in cytochrome P450 2D6 (CYP2D6): Population distribution of CYP2D6 activity.J Toxicol Environ Health B Crit Rev. 2009;12(5-6):334-61. doi: 10.1080/10937400903158342. J Toxicol Environ Health B Crit Rev. 2009. PMID: 20183526 Review.
Cited by
-
Inborn 'errors' of drug metabolism. Pharmacokinetic and clinical implications.Clin Pharmacokinet. 1990 Oct;19(4):257-63. doi: 10.2165/00003088-199019040-00001. Clin Pharmacokinet. 1990. PMID: 2208896 Review. No abstract available.
-
Nonparametric expectation maximisation (NPEM) population pharmacokinetic analysis of caffeine disposition from sparse data in adult caucasians: systemic caffeine clearance as a biomarker for cytochrome P450 1A2 activity.Clin Pharmacokinet. 2003;42(15):1393-409. doi: 10.2165/00003088-200342150-00006. Clin Pharmacokinet. 2003. PMID: 14674790 Clinical Trial.
-
Phenotypic debrisoquine 4-hydroxylase activity among extensive metabolizers is unrelated to genotype as determined by the Xba-I restriction fragment length polymorphism.Br J Clin Pharmacol. 1991 Sep;32(3):283-8. doi: 10.1111/j.1365-2125.1991.tb03900.x. Br J Clin Pharmacol. 1991. PMID: 1685663 Free PMC article.
-
N-Acetyltransferase-2 (NAT2) phenotype is influenced by genotype-environment interaction in Ethiopians.Eur J Clin Pharmacol. 2018 Jul;74(7):903-911. doi: 10.1007/s00228-018-2448-y. Epub 2018 Mar 27. Eur J Clin Pharmacol. 2018. PMID: 29589062 Free PMC article.
-
Phenotypic polymorphism and gender-related differences of CYP1A2 activity in a Chinese population.Br J Clin Pharmacol. 2000 Feb;49(2):145-51. doi: 10.1046/j.1365-2125.2000.00128.x. Br J Clin Pharmacol. 2000. PMID: 10671909 Free PMC article. Clinical Trial.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical