Sentence examples for was correctly imputed from inspiring English sources

Exact(1)

The accuracy of this result, obtained without inspecting the coordinates of the preceding units, can be verified by independently decoding them into symbolic sequences: 000000101000111... and 000000000100000110..., confirming that the length of the shared sequence of 6 zeros was correctly imputed.

Similar(59)

For each individual, imputation accuracy was calculated using the same two measures: (i) the proportion of all of the horses' genotypes that were correctly imputed; and (ii) the correlation between the true and imputed genotypes across all the horses' SNPs when coded as above.

On average, 51.45% of the SNPs have been correctly imputed for all Info values.

a a genotype is correctly imputed if both alleles are correctly imputed.

More than 99% of the alleles were correctly imputed if more than 300 animals were genotyped at high-density.

Specifically, when 87.8% of missing genotypes were correctly imputed, the accuracy of GEBV was reduced by only 5%.

Using Minimac, up to 97.1% of the alleles were correctly imputed based on 50 pre-selected reference animals.

Around 50% of the SNPs were accurately imputed (meaning an accuracy of 100% over all horses) for each animal and the vast majority of the SNPs were correctly imputed in at least 80% of the horses.

Assessing whether the sequence of offspring is correctly imputed can only be done if a sample of such offspring is actually sequenced, and such data are presently not available in sufficient quantities.

In a scenario with low-density genotypes (14 SNPs/Morgan), these authors observed that 87.8% of missing genotypes were correctly imputed but 95% of the accuracy of GEBV obtained with high-density SNP genotypes (1500 SNPs/Morgan) was achieved.

For each imputed SNP, imputation accuracy was assessed using two measures: (i) the proportion of genotypes for the SNP that were correctly imputed among samples; and (ii) the correlation between the true and imputed genotypic allele counts across all samples (homozygote for allele 1, coded 0; heterozygous, coded 1; homozygous for allele 2, coded 2).

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