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A cDNA microarray was established with these cDNAs, and the transcriptional profiles of Thellungiella plants under various stress conditions were obtained [ 8].
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The rapid quantification of bacteria with flow-through chemiluminescence microarrays was established in our laboratories and is applied for bioaerosol analysis in this work.
Tissue microarrays were established as previously described (Zhu et al, 2008).
The correspondence between genes represented by Stanford cDNA microarrays and Rosetta/NKI oligonucleotide microarrays were established by using Unigene identifiers (build 158, release date 18 January 2003 for the wound signature, as this was the original mapping carried out for the validation of the wound signature [ 26]).
Set-up of microarray-database using GEO and EGA-available microarray datasets was established as described previously [ 21].
The University Health Network's Microarray Centre was established as part of a consortium of research institutions in Toronto.
The microarray system was established by determining the method to prepare targets by random-primer labeling with chromosomal DNA and the conditions for hybridization.
To gain insights into the stress responses of R. baltica with respect to salinity and temperature the first whole genome array for R. baltica - also the first Planctomycete microarray - was established and applied.
An oligonucleotide microarray platform was established to detect miRNA signals.
The directional fold change was confirmed for all three genes and the correlation with microarray results was established.
For in silico validation of the genes, a database containing processed GEO microarray samples was established as described earlier (Gyorffy and Schafer, 2009).
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