Suggestions(5)
Exact(7)
In our proposed pipeline, the label for each mapping is determined during the merging stage after considering the mappings to multiple pseudogenomes.
The frequency distribution of a semitone mapping is determined by the number of semitones that are to be mapped over the number of available channels.
The number of markers needed to perform genome-wide association mapping is determined by the extent of LD, or allelic association, in the species or population(s) under investigation.
Step 2: Community mapping to obtain seed protein pairs Community mapping is determined in two steps.
Effectiveness of genomic selection and fine mapping is determined by the level of linkage disequilibrium (LD) across the genome.
Event detection by stochastic mapping is determined by a varying cutoff value (posterior probability of event), thus multiple classifications are possible with various levels of sensitivity (=true positive rate [TPR]) and specificity (=1 − false positive rate [FPR]).
Similar(53)
P-values of LOD scores from the QTL mapping were determined with 1000 genome-wide bootstraps.
The logarithm of odds (LOD) significance threshold for interval mapping was determined by 10,000 iterated permutations.
SNP-based genome-wide association mapping was determined by using TASSEL (Trait Analysis by Association, Evolution and Linkage) software [ 46].
Total numbers of sequence reads for each gene symbol from the transcriptome mapping were determined and were used to create the gene-expression profile matrix.
Genome-wide significance thresholds for linkage mapping were determined by analyzing 1,000 permutations of the phenotype data (Churchill and Doerge 1994).
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