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In order to identify genes with preferential expression in either roots or buttons, an additional two sequencing runs were performed using a PGM™ sequencer (Personal Genome Machine™; Life Techonologies), for which each organ (button and roots) was distinguished by using Ion barcode adapters.
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The three main lineages could be distinguished by using several HRM profiles.
First, the sinensis type and the assamica type groups were distinguished by using the M02 marker.
These two very different scenarios can only be distinguished by using comparisons of ancestors and descendants within lineages or by inferring ancestral characteristics from phylogenies.
At this point, one may raise the following question: if drug-like and non-drug-like molecules can be distinguished by using simple property-based filters.
In practice, thermodynamic phase is distinguished by using polarized reflectance at 0.865 μm given by POLDER and brightness temperature at 10.9μm by OCTS.
Hence these two positional isomers could be distinguished by using their different perturbation effects on a BR dynamic system in the range of 9.0 × 10−4 to 8.0 × 10−3 M.
Modelling studies were distinguished by using patterned bars.
Sedation levels 2, 4, and 6 could thus be distinguished by using spectral entropy.
Individual serotypes within serogroup 6 were distinguished by using serotype-specific PCR.
A subset, however, is distinguished by using synaptic zinc as cofactor.
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