Your English writing platform
Discover LudwigExact(12)
The genotype at a marker locus is coded as 0, 1 or 2, corresponding to the copy number of an arbitrary allele.
Without making any assumptions about the distributions of the phenotypes, the multivariate FBAT test allows us to test the null hypothesis that the marker locus is not linked to any genetic locus that has an influence on the selected phenotypes.
The minor-allele frequency at each marker locus is at least 10%.
Fitting the mixed model described in equation {2} for each SNP marker locus is currently infeasible without approximations [ 34].
Here, the genetic variance explained by each marker locus is evaluated and different weights are thereby given to different genomic regions in the EBV calculation.
Furthermore, more alleles can be taken into account simultaneously and therefore, the probability that at least one population is polymorphic at a given marker locus is higher.
Similar(48)
Both the disease locus and marker locus were simulated to be diallelic, with the marker allele frequencies = .5 and the disease allele frequency = .25.25
Since marker allele-disease association and linkage between a disease locus and a marker locus are two different events, linkage without evidence of association and association without evidence of linkage are possible observations [22].
The QTL effect of each marker locus was investigated in the full TBBC3 population.
Genotype frequencies at every marker locus are given in Additional file 1: Table S1.
Within each set of NILs, lines contrasting for each marker locus were grouped and analyzed for their phenotypic differences.
More suggestions(1)
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