Your English writing platform
Discover LudwigSuggestions(2)
Exact(1)
The authors applied the proportion reactivated, calculated from the observed data, to persons with missing genotypes, thus amplifying any misclassification.
Similar(59)
Minimizing the conditional variance based on the A matrix (MCA ) makes sense since the aim is to predict the missing genotypes and thus, conditional on (dense) genotypic information, to minimize the unexplained genetic variation.
We were not able to detect interaction between ScIce2 and ScCbf9b probably due to the large number of rare haplotypes (MAF < 5%) in ScCbf9b resulting in missing genotypes (87.9%) and thus in insufficient statistical power to identify gene × gene interaction.
The performance of the genotyping assay for each method was assessed using three criteria: missing genotypes (assay fail rates), incomplete genotypes (loci departing from HWE) and inaccurate genotypes (inconsistent genotypes across replicate samples).
This has resulted in high rates of missing genotypes (assay fail rates of 21%), incomplete genotypes (64% of loci departing from HWE) and inaccurate genotypes (1% of genotypes inconsistent across replicates).
SNPs with ≥2 missing genotypes were excluded.
The overall rate of missing genotypes was 9%.
Based on estimated parameters, missing genotypes are inferred.
Samples were screened for the proportion of missing genotypes, and animals with greater than 10% missing genotypes were removed.
Regarding missing genotypes, PGMDR discards families entirely when data on one SNP are missing.
This software estimates the missing genotypes and reconstructs haplotypes using unphased genotype data from unrelated individuals.
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com