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Since the resequencing microarray is not sensitive enough to differentiate individual recombinants, the minor genotypes identified by the resequencing analysis could very well represent composites of these recombinant genomes.
A high-density oligonucleotide microarray is not yet available for global transcript profiling of common bean.
A high-density oligonucleotide microarray is not yet available for global transcript profiling in alfalfa.
The traditional method of transcriptome profiling, gene expression microarray, is not sensitive in distinguishing transcripts among very similar gene sequences.
Thirdly, the microarray is not a complete survey of the transcriptome and so there will be sex genes and sex-biased genes that were not surveyed.
Whether or not the shape of the distribution changes if the data are collected by microarray is not clear, and further refinement awaits direct RNA sequencing count data.
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Approximately half of the highly expressed genes identified in the 135k microarray are not included in the previous microarray.
FGF4 and Cacnb3, although displayed on the microarray, were not amplified by qRT-PCR.
This microarray was not designed to be diagnostic; by using whole-genome arrays for each virus, probes were designed independent of degree of cross-hybridization.
However, it is evident that the overall expression alteration of all 25 genes is statistically comparable, although the actual fold change values in real-time PCR and microarray are not always commensurable.
Since most of the miRNAs used on the microarray are not present at detectable levels in most serum samples, clustering was only performed on a subset of the miRNAs.
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