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The genomic distance over which LD persists will determine the number and density of markers needed to perform a genome-wide association analysis.
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.
The main problem of the synaptic Brainbow at this time is the large number of fluorescent markers needed to map a large neural circuit.
However, due to an incomplete understanding of fibroblast development from MSCs and to their cellular heterogeneity in vivo that results in a lack of definitive markers needed to isolate them [15], [16], realization of the therapeutic potential of fibroblasts has been limited [17].
Further studies including other inflammatory markers needed to confirm our results.
With LD spanning a short distance, the resolution of association mapping will be excellent, but the number of markers needed to cover the genome is high.
Similar(42)
However, all the predicted molecular markers need to be validated.
But the markers need to be removed by linear interpolatioin further.
However, additional molecular markers needs to be screened for identifying potential recombination events which can help in higher resolution mapping to determine the gene underlying qBK1.2 precisely.
However, allele-specific markers for yield-enhancing genes have not been developed yet for some major yield-enhancing genes or the existing markers need to be improved for an effective marker-assisted breeding program.
Therefore, multiple markers need to be analyzed simultaneously in order to distinguish these innate cell populations.
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