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Exact(29)
The 3xP3-EGFP marker was tested in mosquitoes with different genetic backgrounds.
The DEP1-indel1 marker was tested in the donor and 12 recipients, and it discriminated DEP1 alleles clearly (Fig. 5b).
This marker was tested in the parental varieties, and the result was consistent with the Gn1a-17 SNP marker analysis, except for Parao (Fig. 1b middle), indicating that the marker is available to introduce Gn1a-Habataki allele into Gn1a-Type 2 backgrounds but not Parao background.
Each marker was tested in two replicates and their average was used in the statistical analysis.
Expression of mRNA encoding Myf5 early myogenic differentiation marker was tested by real time PCR.
Each genetic marker was tested for Hardy-Weinberg equilibrium in the control population.
Similar(31)
We found power was increased by excluding markers that are in LD with the marker being tested.
Phylogenetic utility of the markers was tested in two genera, Gnomoniopsis and Ophiognomonia (Gnomoniaceae, Diaporthales).
The effectiveness of flanking markers was tested in a segregating population and the InDel type markers PA26 and RM2334 showed high co-segregation with the resistance phenotype.
The linkage of the markers was tested based on the LOD score (the threshold of the LOD score was 3.0, and the maximum distance was 25 cM).
In addition, the anti-soiling and anti-graffiti performance against inorganic dusts, carbonaceous pollutants and permanent markers was tested according to standardized procedure.
Related(20)
trace was tested
marker was evidenced
marker was established
gauge was tested
indicator was tested
marker was analyzed
score was tested
marker was inspected
marker was estimated
marker were tested
marker was built
marker was switched
marker was lost
marker was dedicated
marker was verified
marker was elevated
marker was removed
marker was located
marker was used
marker was unveiled
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