The DOI matches its Crossref record; 21 of the 21 references it cites were found in a registry or an index.
A simple correction for multiple comparisons in interval mapping genome scans
Open accessAbstract
Several approaches have been proposed to correct point-wise significance thresholds used in interval-mapping genome scans. A method for significance threshold correction based on the Bonferroni test is presented. This test involves calculating the effective number of independent comparisons performed in a genome scan from the variance of the eigenvalues of the observed marker correlation matrix. The more highly correlated the markers, the higher the variance of the eigenvalues and the lower the number of independent tests performed on a chromosome. This approach was evaluated by mapping 1000 normally distributed phenotypes along chromosomes of varying length and marker density in a population size of 500. Experiment-wise significance thresholds obtained from the simulation are compared to those calculated using the Bonferroni criterion and the newly developed measure of the effective number of independent tests in a genome scan. The Bonferroni calculation produced significance thresholds very similar to those obtained by simulation. The threshold levels for both Bonferroni and simulation analysis depended strongly on the marker density and size of chromosomes. There was a slight bias of about 1% in the thresholds obtained at the 5% and 10% point-wise significance levels. The method introduced here provides a relatively simple correction for multiple comparisons that can be easily calculated using standard statistics packages.
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“Modifications to the Bonferroni correction in the context of QTL mapping have been proposed by Cheverud (2001), and further modifications proposed by Li and Ji (2005).”
From The statistical analysis of multi-environment data: modeling genotype-by-environment interaction and its genetic basis (2013) · cites this paper as Cheverud (2001)
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Cites
Genetics and Analysis of Quantitative Traits
(2002) · Journal of Animal Breeding and Genetics · doi:10.1046/j.1439-0388.2002.00356.x · Cited by 6,176
Mapping mendelian factors underlying quantitative traits using RFLP linkage maps.
Lander, E. S., & Botstein, D. (1989) · Genetics · doi:10.1093/genetics/121.1.185 · Cited by 5,236
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
Lander, E. S., & Kruglyak, L. (1995) · Nature Genetics · doi:10.1038/ng1195-241 · Cited by 5,236
Empirical threshold values for quantitative trait mapping.
Churchill, G. A., & Doerge, R. W. (1994) · Genetics · doi:10.1093/genetics/138.3.963 · Cited by 4,935
Precision mapping of quantitative trait loci.
Zeng, Z. B. (1994) · Genetics · doi:10.1093/genetics/136.4.1457 · Cited by 3,182
Weir, B. S. (1997) · Biometrics · doi:10.2307/2533134 · Cited by 2,263
Haley, C. S., & Knott, S. A. (1992) · Heredity · doi:10.1038/hdy.1992.131 · Cited by 1,991
Genetic dissection of complex traits
Witte, J., Elston, R., & Schork, N. (1996) · Nature Genetics · doi:10.1038/ng0496-355 · Cited by 1,883
Hill, W. G. (1996) · Genetics Research · doi:10.1017/s0016672300034121 · Cited by 921
Multiple trait analysis of genetic mapping for quantitative trait loci.
Jiang, C., & Zeng, Z. (1995) · Genetics · doi:10.1093/genetics/140.3.1111 · Cited by 831
Cheverud, J. M., Rutledge, J. J., & Atchley, W. R. (1983) · Evolution · doi:10.1111/j.1558-5646.1983.tb05619.x · Cited by 297
Self-citationMethods for the Comparative Analysis of Variation Patterns
Cheverud, J. M., Wagner, G. P., & Dow, M. M. (1989) · Systematic Zoology · doi:10.2307/2992282 · Cited by 296
Self-citationWagner, G. P. (1984) · Journal of Mathematical Biology · doi:10.1007/bf00275224 · Cited by 269
Cheverud, J. M. (1996) · Journal of Evolutionary Biology · doi:10.1046/j.1420-9101.1996.9010005.x · Cited by 222
Self-citationGenetic architecture of adiposity in the cross of LG/J and SM/J inbred mice
Cheverud, J. M., Vaughn, T. T., Pletscher, L. S., Peripato, A. C., Adams, E. S., Erikson, C. F., & King‐Ellison, K. (2001) · Mammalian Genome · doi:10.1007/s003350010218 · Cited by 146
Self-citationApproximate thresholds of interval mapping tests for QTL detection.
Rebaï, A., Goffinet, B., & Mangin, B. (1994) · Genetics · doi:10.1093/genetics/138.1.235 · Cited by 128
A comparative study of morphological integration in Apis mellifera (Insecta, Hymenoptera)
Wagner, G. P. (2009) · Journal of Zoological Systematics & Evolutionary Research · doi:10.1111/j.1439-0469.1990.tb00364.x · Cited by 104
A COMPARATIVE ANALYSIS OF MORPHOLOGICAL VARIATION PATTERNS IN THE PAPIONINS
Cheverud, J. M. (1989) · Evolution · doi:10.1111/j.1558-5646.1989.tb02623.x · Cited by 101
Self-citationDarvasi, A., & Soller, M. (1994) · Theoretical and Applied Genetics · doi:10.1007/bf00225166 · Cited by 84
Genetic dissection of complex traits
Lander, E. S. (1996) · Nature Genetics · doi:10.1038/ng0496-357 · Cited by 70
Genetic dissection of complex traits
Curtis, D. (1996) · Nature Genetics · doi:10.1038/ng0496-356 · Cited by 54
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Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix
Li, J., & Ji, L. (2005) · Heredity · doi:10.1038/sj.hdy.6800717 · Cited by 1,458
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Madsen, B. E., & Browning, S. R. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000384 · Cited by 1,113
Implementing false discovery rate control: increasing your power
Verhoeven, K. J. F., Simonsen, K. L., & McIntyre, L. M. (2005) · Oikos · doi:10.1111/j.0030-1299.2005.13727.x · Cited by 964
Li, M.-X., Yeung, J. M. Y., Cherny, S. S., & Sham, P. C. (2012) · Human Genetics · doi:10.1007/s00439-011-1118-2 · Cited by 962
Metadata
- Authors
- Cheverud, J. M.
- Affiliations
- Washington University in St. Louis (US)
- Corresponding author
- Cheverud, James M
- ORCID
- Cheverud, James M
- Venue
- Heredity
- Published
- 2001
- Volume
- 87
- Issue
- 1
- Pages
- 52-58
- ISSN
- 0018-067X (ISSN-L)
- OpenAlex
- W2054881132
- Cited by
- 421
- References
- 21
- Citations by year
- 2026: 8 · 2025: 16 · 2024: 13 · 2023: 10 · 2022: 21 · 2021: 21 · 2020: 18 · 2019: 9 · 2018: 17 · 2017: 10 · 2016: 30 · 2015: 21 · 2014: 14 · 2013: 24 · 2012: 25
- FWCI
- 3.43
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Heredity (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Science Foundation (9726433)
- National Institutes of Health (5r01dk052514-06)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK52514)
- Division of Environmental Biology
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Mapping and Diversity in Plants and Animals
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and phenotypic traits in livestock
- Keywords
- multiple testing correction, interval mapping, genome scan, Bonferroni correction, significance threshold, marker density, chromosome length, QTL mapping
- MeSH terms
- Analysis of Variance, Biometry, Chromosome Mapping, Computer Simulation, Genetic Markers, Genotype, Genetic Linkage, Models, Genetic, Statistics as Topic, Models, Statistical, Quantitative Trait, Heritable
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