This method defines a genomic signature as a set of frequencies of all overlapping oligonucleotides of specific length k (k = 4 in this study) in the forward strand of the whole nucleotide sequences available for a given genome.
The first stage (at least, after the atoms have been cooled close to absolute zero by more traditional methods) involves an optical "trap"—a set of lasers emitting frequencies of light that slow the atoms down.
This is performed by assuming harmonicity of the sources and by the use of a frequency threshold that assigns a set of frequency bins to a given harmonic.
In [31], the magnitude of impedance at PCC is compared with that of a set of frequency dependent reference for ID.
In this work, spectrum sensing for cognitive radios is considered in the presence of multiple Primary Users (PU) using frequency-hopping communication over a set of frequency bands.
The modulation frequency filterbank is implemented as a set of frequency domain filters.
In section 3, we extend this method through the minimization of a criterion intended to jointly equalize energies of signals in a set of frequency subin-tervals.
The method uses a set of frequency transformations to translate the multimedia data into the frequency domain.
Figure 3 displays the fraction of sites discovered within a set of frequency ranges.
As a consequence of these alterations dynamic characteristics of the beam are changed revealing a set of frequency band gaps.
Besides, this method possesses an order-independent nature, which means that even the order of contigs of a genome is unknown, the probe-set frequencies of the genome can still be accurately obtained.
