Practical optical amplification in silicon is therefore very desirable.
Previously, the single-locus SSR markers were developed by practical PCR amplification in a panel of inbred lines, which was time consuming, labour intensive, high cost and, thus, inefficient.
Simulation results indicate that the optical path design is attractive in realizing the high gain of Tm3+ doped germanate glass channel waveguides for practical S-band amplification.
The development of practical Erbium Doped Fiber Amplification (EDFAs) enabled the development of dense Wavelength Division Multiplexing (WDM) optical networks.
For RT-qPCR experiments on single or a few genes, dilution series are needed and practical for estimating amplification efficiencies, which can then be taken into account in normalization.
The simulation results indicate that the bent structure designing is beneficial in attaining high optical gain in Er3+/Yb3+ codoped germanate glass substrates, which assures that long-period grating can be applied to implement practical C-band gain-flattened amplification.
Practical factors, such as PCR amplification efficiency, have not been taken into our theoretical consideration.
Microdissection of chromosomes has been attempted, but this approach depends on whole-genome amplification due to practical limits on the amount of starting material [ 17].
Taken together with our previous studies ([6],[8]; Mariani et al. 1996b; [7],[13],[14]), the findings reported here suggest the following practical approach to applying the PCR amplification technology for the diagnosis of infectious diseases.
Whole genome amplification (WGA) promises to eliminate practical molecular genetic analysis limitations associated with genomic DNA (gDNA) quantity.
