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For these microarray technologies, the number of available tools is small compared with mRNA analysis tools.
For most microarray technologies, the set of potential targets must be available in advance so that appropriate probe sequences can be used.
Here we describe a systematic comparison of data from four leading microarray technologies (the Affymetrix Genome-wide SNP 5.0 array, Agilent High-Density CGH Human 244A array, Illumina HumanCNV370-Duo DNA Analysis BeadChip, and the Nimblegen 385 K oligonucleotide array).
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Currently, many gene-expression studies use microarray technology, the basis for which is RNA transcript hybridizing to immobilized probes which correspond to tens of thousands of defined sequences.
More recently Carmichael and colleagues studied by microarray technology the genomic patterns in acute ICH (<24 hours) compared to healthy brains.
Furthermore, with the continuing development of microarray technology, the capacity of microarrays is expected to increase.
The ChIP-on-chip technique combines chromatin immunoprecipitation (the ChIP) with DNA microarray technology (the chip).
Compared with the previous microarray technology, the RNA-seq approach offers several obvious advantages.
Compared to microarray technology, the RNAseq method offers several distinct advantages.
There are several types of microarray technologies currently in use with studies using oligonucleotide microarray technology, the most common for high-throughput quantitative studies of RNA expression (47).
Due to the success of microarray technology, the available data on the transcriptional regulatory networks of different organisms has grown exponentially.
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