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Codominant markers are adequate tools to test the autotetraploid structure of the genome [ 22].
Conclusions: These highly polymorphic markers are adequate for DNA profiling and studies of population genetics in S. platyclados.
Conclusions: These results indicate that these microsatellite markers are adequate for detecting and characterizing population genetic structure in the Chinese species of sect.
Conclusions: Levels of polymorphism of the reported markers are adequate for studies of diversity and fragmentation in natural populations of this parasitic plant.
Observed levels of polymorphism suggest that the reported markers are adequate for characterizing spatial genetic structure at reduced spatial scales and for studying aggregation patterns in Phoradendron host-parasite relationships.
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This reduced set of markers was adequate for MIBD evaluation, as the close connections among the inbred pedigree has led to IBD sharing over long chromosomal segments.
Our findings indicate that, the different measures of marker informativeness [δ, FST, FIC, SIC, and In] performed well and as few as the top 20 ranked informative markers were adequate for accurate classification of ancestral populations.
These analyses suggest that while the neuronal proportion prediction accuracy is optimized with large sets of CETS markers, the performance of the algorithm in subset of these markers is adequate to generate accurate predictions and is dependent only on relative methylation as opposed to absolute methylation signals.
This analysis revealed that a single, unique molecular marker is adequate for discrimination of the noninfiltrative versus infiltrative/invasive tumors.
For the non-carrier chromosomes, two markers per arm are adequate, although additional markers may further increase accuracy of the RPG recovery estimates.
When we ran STRUCTURE with K set to 7 using 25 of the 42 microsatellites, i.e. those we had used in our previous study [21], clustering of the six units was not observed (data not shown), suggesting that these 25 markers are not adequate for a fine-scale phylogenetic study of the A. gambiae complex, particularly when one aims to characterize the closely related A. gambiae s.s.s
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