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The studies of gene expression variability started relatively lately, with the advent of high-throughput technologies of analysis [1], [2].
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The development of an ever-expanding armamentarium of technologies for analysis of gene structure and function, referred to as recombinant DNA (deoxyribonucleic acid) technology, has created unprecedented opportunities for significantly improving the treatment and prevention of human diseases.
Using the combined technologies of FE analysis and 3D reconstruction of the middle ear from HRCT, we developed an FE model of the human middle ear with TM, ossicular bone, middle ear ligament, and middle ear boundaries [23].
In conclusion, the now standardized technologies of epigenome analysis coupled with whole-genome expression studies are required to determine the biological and clinical impact of environmentally induced epigenetic modifications in humans.
It is known from similar studies that the two technologies of expression analysis deliver qualitatively comparable data, however, the magnitude of such expression changes as reflected by microarray data tends to be generally compressed in comparison with qRT PCR [ 16].
Performing whole genome association (WGA) scans in ALS, as well as in other disorders, depends on robust technologies for analysis of individual SNP variants.
We report the first use of this technology for analysis of gene expression in filarial male and female worms.
These results show the utility of chip technology for analysis of rheumatoid disease.
It shows a versatility of the cell array technology for analysis of gene sets at various levels of genetic information flow.
Survival analysis is a technology of statistical analysis about survival time.
The high-density cDNA array technology to analysis of H. parasuis-infected PAM could improve our understanding of the H. parasuis infection.
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