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The genotype data were analyzed after one round of genotyping, and then based on the results we got, we chose new SNPs for new assays, according to their positions and functional importance, as well as the requirement of maximizing the number of genes included in the iPLEXes to be studied to increase the marker coverage density.
We have utilized the recently developed sugarcane DArT array to increase the marker density within the genetic map.
Based on these results, nine additional families were genotyped and analysed to increase the marker density in regions of interest.
As the major objective is to increase the marker density on the map, here we reported a sex-averaged map rather than sex-specific map.
In the process, we sought to also increase the marker density and utility of the catfish genetic linkage map for genomic studies.
In an effort to increase the marker density for sugarcane, a diversity array was developed using a combination of S. officinarum and S. spontaneum accessions and sugarcane cultivars [[ 23]].
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Therefore, increasing the size of training population rather than increasing the marker number can be preferable for rice hybrid prediction.
Eventhough some major effect QTLs were identified for three traits, the results could have been improved by increasing the marker density and the population size.
Nine polymorphic SSR markers were applied to narrow down the putative location responsible for the floury endosperm characteristics by increasing the marker density of chromosome 5 (Table 4; Locus, Ap = 2).
Results indicate that increasing the marker density increased the prediction ability of the models for most trait environment combinations.
The weak estrogen E3 (Clark and Markaverich 1984; Katzenellenbogen 1984; Lan and Katzenellenbogen 1976) also increased the marker.
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