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Imputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohortImproved imputation of low-frequency and rare variants using the UK10K haplotype reference panelHigh-accuracy haplotype imputation using unphased genotype data as the referencesReferences for Haplotype Imputation in the Big Data Era.Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studies.Choosing Subsamples for Sequencing Studies by Minimizing the Average Distance to the Closest LeafLatitudinal Clines of the Human Vitamin D Receptor and Skin Color Genes.Genotype imputation reference panel selection using maximal phylogenetic diversity.A pharmacokinetic/pharmacodynamic model of tumor lysis syndrome in chronic lymphocytic leukemia patients treated with flavopiridol.Imputation of rare variants in next-generation association studies.Theory and applications of a deterministic approximation to the coalescent model.Across-Platform Imputation of DNA Methylation Levels Incorporating Nonlocal Information Using Penalized Functional Regression.Genotype imputation in a coalescent model with infinitely-many-sites mutation.Imputation of missing genotypes within LD-blocks relying on the basic coalescent and beyond: consideration of population growth and structure.
P2860
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P2860
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
A coalescent model for genotype imputation.
@ast
A coalescent model for genotype imputation.
@en
type
label
A coalescent model for genotype imputation.
@ast
A coalescent model for genotype imputation.
@en
prefLabel
A coalescent model for genotype imputation.
@ast
A coalescent model for genotype imputation.
@en
P2860
P1433
P1476
A coalescent model for genotype imputation
@en
P2093
Ethan M Jewett
Sebastian Zöllner
P2860
P304
P356
10.1534/GENETICS.111.137984
P407
P577
2012-05-17T00:00:00Z