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Assessment of genotype imputation methods.

BMC proceedings | 2009

Several methods have been proposed to impute genotypes at untyped markers using observed genotypes and genetic data from a reference panel. We used the Genetic Analysis Workshop 16 rheumatoid arthritis case-control dataset to compare the performance of four of these imputation methods: IMPUTE, MACH, PLINK, and fastPHASE. We compared the methods' imputation error rates and performance of association tests using the imputed data, in the context of imputing completely untyped markers as well as imputing missing genotypes to combine two datasets genotyped at different sets of markers. As expected, all methods performed better for single-nucleotide polymorphisms (SNPs) in high linkage disequilibrium with genotyped SNPs. However, MACH and IMPUTE generated lower imputation error rates than fastPHASE and PLINK. Association tests based on allele "dosage" from MACH and tests based on the posterior probabilities from IMPUTE provided results closest to those based on complete data. However, in both situations, none of the imputation-based tests provide the same level of evidence of association as the complete data at SNPs strongly associated with disease.

Pubmed ID: 20018042 RIS Download

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: R01 CA122443
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM031575
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM031575-28

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This is a list of tools and resources that we have found mentioned in this publication.


IMPUTE (tool)

RRID:SCR_009245

Software application for estimating (imputing) unobserved genotypes in SNP association studies. The program is designed to work seamlessly with the output of the genotype calling program CHIAMO and the population genetic simulator HAPGEN, and it produces output that can be analyzed using the program SNPTEST. (entry from Genetic Analysis Software)

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MACH (tool)

RRID:SCR_009621

QTL analysis based on imputed dosages/posterior_probabilities.

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