ArticleBMC research notes2012
Fast accurate missing SNP genotype local imputation.
Article in BMC research notes, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- Parentage and relatedness reconstruction in Pinus sylvestris using genotyping-by-sequencing.Heredity · 2020Article
- JS-MA: A Jensen-Shannon Divergence Based Method for Mapping Genome-Wide Associations on Multiple Diseases.Frontiers in genetics · 2020Article
- Efficient analysis of large-scale genome-wide data with two R packages: bigstatsr and bigsnpr.Bioinformatics (Oxford, England) · 2018Article
- Comparison of three boosting methods in parent-offspring trios for genotype imputation using simulation study.Journal of animal science and technology · 2016Article
- Whole genome SNP genotype piecemeal imputation.BMC bioinformatics · 2015Article
- Cloud computing for detecting high-order genome-wide epistatic interaction via dynamic clustering.BMC bioinformatics · 2014Article
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundSingle nucleotide polymorphism (SNP) genotyping assays normally give rise to certain percents of no-calls; the problem becomes severe when the target organisms, such as cattle, do not have a high resolution genomic sequence. Missing SNP genotypes, when related to target traits, would confound downstream data analyses such as genome-wide association studies (GWAS). Existing methods for recovering the missing values are successful to some extent - either accurate but not fast enough or fast but not accurate enough.
resultsTo a target missing genotype, we take only the SNP loci within a genetic distance vicinity and only the samples within a similarity vicinity into our local imputation process. For missing genotype imputation, the comparative performance evaluations through extensive simulation studies using real human and cattle genotype datasets demonstrated that our nearest neighbor based local imputation method was one of the most efficient methods, and outperformed existing methods except the time-consuming fastPHASE; for missing haplotype allele imputation, the comparative performance evaluations using real mouse haplotype datasets demonstrated that our method was not only one of the most efficient methods, but also one of the most accurate methods.
conclusionsGiven that fastPHASE requires a long imputation time on medium to high density datasets, and that our nearest neighbor based local imputation method only performed slightly worse, yet better than all other methods, one might want to adopt our method as an alternative missing SNP genotype or missing haplotype allele imputation method.
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