The NM-CGH microarray method is currently available for mutation analysis in our laboratory.
The DNA microarray method is found to be more sensitive in comparison to labor-intensive semiquantitative RT-PCR method, which gives data for a few gene transcripts.
A microarray method was developed for the detection of 40 bacterial species reported in the literature to be predominant in the human gastrointestinal tract.
The microarray method was used to screen fecal samples obtained from 11 healthy human volunteers for the presence of these intestinal bacteria.
Thus, the microarray method is a device with high specificity and less sensitivity, compared to the Taqman assay.
The results, however, clearly indicated that the present microarray method was very efficient for screening the genes differentially expressed in SRCBs.
Validation of our microarray method was done by comparing the results for LINE-1 to pyrosequencing data in the same colorectal samples.
The ratio magnification was also observed when the ADGE microarray method was applied to the whole microarray chip.
A DNAzyme-based microarray method was developed by Zuo et al. to detect multiple metal ions (Zuo et al., 2009).
The protein microarray method is currently being established as a powerful tool for detecting proteins, observing their expression levels, and probing their interactions and functions.
