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MOESM4 of Genotyping by low-coverage whole-genome sequencing in intercross pedigrees from outbred founders: a cost-efficient approach

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posted on 2019-08-15, 05:00 authored by Yanjun Zan, Thibaut Payen, Mette Lillie, Christa Honaker, Paul Siegel, Örjan Carlborg
Additional file 4: Figure S4. Illustration of relationship between sequencing coverage, SNP density and imputation accuracy. (a/b) Histograms of the sequencing coverage/SNP densities for the 803 genotyped F2 individuals; (c/d) Scatter plots of individual coverage/SNP density vs imputation accuracy measured as proportion of sites that has same genotype with the averaged genotype probabilities estimated by Wahlberg et al. [21] using genotypes of 434 SNPs and microsatellite markers with the Haley and Knott algorithm [32].

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Svenska ForskningsrĂĽdet Formas (SE)

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