Comparison of type I error for multiple test corrections in large single-nucleotide polymorphism studies using principal components versus haplotype blocking algorithms
2005

Comparison of Type I Error for Multiple Test Corrections in SNP Studies

Sample size: 143 publication Evidence: moderate

Author Information

Author(s): Kristin K Nicodemus, Wenlei Liu, Gary A Chase, Ya-Yu Tsai, M Daniele Fallin

Primary Institution: Johns Hopkins Bloomberg School of Public Health

Hypothesis

Can different methods for correcting type I error rates in SNP studies provide more accurate results?

Conclusion

Using linkage disequilibrium block-based corrections can prevent type I error inflation in SNP studies without being overly conservative.

Supporting Evidence

  • Permutation testing is time-consuming but was previously the gold standard for significance levels.
  • Bonferroni correction is not suitable due to correlations between tests in SNP settings.
  • The study found that the blocking algorithm corrections are closest to the desired type I error under moderate LD.

Takeaway

This study looks at how to avoid mistakes when testing many genes at once. It finds a better way to check if the results are real.

Methodology

The study simulated parent-child trio data under different linkage disequilibrium conditions and compared various correction methods for type I error rates.

Limitations

The study did not consider low LD conditions, which may affect the applicability of the findings.

Participant Demographics

The study used simulated data from the Collaborative Study on the Genetics of Alcoholism.

Digital Object Identifier (DOI)

10.1186/1471-2156-6-S1-S78

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication