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Recently, a second-generation array containing ~7000 SNP markers, referred to as the C7AIR, was designed by removing poor-performing SNPs from the C6AIR and adding markers selected to increase the utility of the array for elite tropical japonica material.
This demonstrates the utility of the array for carrying out comparisons between Apis species.
It confirms the utility of the array for a wide range of applications in maize germplasm.
Without regard for the identity of the array features, hybridization dynamics inform on the utility of the array.
We clearly show the utility of the array for heterologous hybridization across a range of fish species for which there is no other microarray available.
The similarity of the elicited transcriptional signatures observed on the arrays hybridized with the N. longiflora and N. attenuata [ 13] probes demonstrates the utility of the array in the analysis of samples from congenerics.
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To determine the utility of the arrays in the analysis of responses from congenerics, arrays were hybridized with samples taken from two tetraploid species (N.
In particular we were interested to test a set of immunological gene probes on our chicken microarrays to see if they provide functionally useful results, thus revealing the utility of the arrays in cross-species studies.
We show the utility of this array for the sensitive detection of these pathogens from complex substrates like soil, plant tissues and irrigation water, and samples that are collected by tomato growers in their greenhouses.
To demonstrate the utility of this array platform, we have analyzed the patterns of promoter usage in 17β-estradiol (E2 -treated and untrE2 -treatedcells and show widespread untreatedalternative proMCF7rs.
We first compared the platforms at the gene expression level and concluded that the Gene Array results are highly concordant with the Exon Array results, reaffirming the utility of the Gene Array as a gene expression profiling tool.
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