Microarrays were washed, stained, and scanned according to standard procedures.
DNA microarrays were washed as described and read using an Applied Biosystems 1700 Chemiluminescent Microarray Analyzer.
Microarrays were washed and scanned using an Agilent Scanner controlled by Agilent Scan Control 7.0 software.
Microarrays were washed and stained using the Affymetrix Fluidics Station FS400.
After hybridization, the microarrays were washed with Oligo aCGH wash buffer followed by drying of slides.
Microarrays were washed in ddH2O five times, once in isopropanol, then dried immediately by centrifugation.
After hybridization the microarrays were washed and dried according to the procedures described in the manufacturer's protocol.
Following a 16-h incubation the microarrays were washed and scanned using the EukGE-WS2v4 fluidics protocol.
The microarrays were washed to remove non-bound streptavidin, dried, and fluorescent binding events measured by a GenePix 4000B.
Finally, the microarrays were washed and fluorescence signals of the hybridized Agilent Microarrays were detected using Agilent's Microarray Scanner System.
The microarrays were washed and stained using an Affymetrix Fluidics Station 450 according to the manufacturer's standard protocol and scanned using the Affymetrix GeneChip Scanner 3000 (Affymetrix).
