Evidence map›Paper›PMID 26498158›Full record

ArticleBMC bioinformatics2015

Whole genome SNP genotype piecemeal imputation.

Yining Wang, Tim Wylie, Paul Stothard, Guohui Lin

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Article in BMC bioinformatics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yining WangDepartment of Computing Science, University of Alberta, Edmonton, Alberta T6G 2E8, Canada. yining@ualberta.ca.
Tim WylieDepartment of Computing Science, University of Alberta, Edmonton, Alberta T6G 2E8, Canada. timothy.wylie@utrgv.edu.
Paul StothardDepartment of Agricultural, Food, and Nutritional Science, University of Alberta, Edmonton, T6G 2C8, Alberta, Canada. stothard@ualberta.ca.
Guohui LinDepartment of Computing Science, University of Alberta, Edmonton, Alberta T6G 2E8, Canada. guohui@ualberta.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite ongoing reductions in the cost of sequencing technologies, whole genome SNP genotype imputation is often used as an alternative for obtaining abundant SNP genotypes for genome wide association studies. Several existing genotype imputation methods can be efficient for this purpose, while achieving various levels of imputation accuracy. Recent empirical results have shown that the two-step imputation may improve accuracy by imputing the low density genotyped study animals to a medium density array first and then to the target density. We are interested in building a series of staircase arrays that lead the low density array to the high density array or even the whole genome, such that genotype imputation along these staircases can achieve the highest accuracy.

resultsFor genotype imputation from a lower density to a higher density, we first show how to select untyped SNPs to construct a medium density array. Subsequently, we determine for each selected SNP those untyped SNPs to be imputed in the add-one two-step imputation, and lastly how the clusters of imputed genotype are pieced together as the final imputation result. We design extensive empirical experiments using several hundred sequenced and genotyped animals to demonstrate that our novel two-step piecemeal imputation always achieves an improvement compared to the one-step imputation by the state-of-the-art methods Beagle and FImpute. Using the two-step piecemeal imputation, we present some preliminary success on whole genome SNP genotype imputation for genotyped animals via a series of staircase arrays.

conclusionsFrom a low SNP density to the whole genome, intermediate pseudo-arrays can be computationally constructed by selecting the most informative SNPs for untyped SNP genotype imputation. Such pseudo-array staircases are able to impute more accurately than the classic one-step imputation.

Indexed as

Genome-Wide Association StudyAnimalsCattleCluster AnalysisGenomeGenotypePolymorphism, Single NucleotideSoftware

Identifiers

PMID26498158
PMCPMC4619096

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.