This allows us to approximate the gap between the heritability already explained by the discovered cis- and trans-eQTLs and the heritability accessible with our SNP microarray technology in even larger studies.
Genomic sequencing, in contrast to genotyping microarray technology, reveals rare or even unique alleles lacking scientific literature support for physiological effects.
Currently, microarray technology is less expensive and even more developed, in comparison to other techniques applied in proteomic and metabolomic research.
In the near future, a new generation of sequencing techniques will help overcome limited genome sequence availability; they will also greatly supplement, and potentially even replace, microarray technology in the coming years.
Comparison of the data between rat and mouse have been made and showed the difficulties to compare the different zones of these two mammalians epididymis, even using similar microarray technology [ 20, 45].
With the continuing advancement of protein microarray technology, this microarray could be expanded to hundreds or even thousands of allergens, providing an efficient and economically feasible assay to measure allergen-specific IgE in sera.
Additionally, our analyses here suggest the ability of these procedures to allow interrogation of classes of rare transcripts, even at impressively low input RNA amounts, for which microarray technology is widely believed to be insufficiently sensitive.
Microarray technology allows large-scale and parallel measurements for expression of around thousands, perhaps even tens of thousands, of genes.
Modern microarray technology is capable of providing data about the expression of thousands of genes, and even of whole genomes.
Microarray technology presented in this paper yielded an in depth analysis of diversity for lettuce germplasm separating even closely related lines such as the crisphead class.
Even with the high sensitivity of today's proteomics methods, proteome coverage is low compared to microarray technology.
