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Type II regions correspond to bands that were observed in seven tissues but displayed different methylation patterns; these bands were defined as tissue-polymorphic methylation fragments.
Type I regions correspond to bands that were only observed in one tissue or bands that were found in six tissues but not in the seventh tissue; these bands were defined as tissue-specific methylation fragments.
Isolates that differed by 1 to 3 bands were defined as a subtype.
After calculation of amplitudes of the spontaneous brain activity, frequency bands were defined as delta (1.3 4.0 Hz), alpha (8.0 12.0 Hz), low gamma (30.5 49.0 Hz), and high gamma (50.3 70.20 Hz).
Isolates with identical patterns were considered genotypically "indistinguishable", while those that differed by 1 to 3 bands were defined as "closely related" and 4 to 6 bands as "possible related".
PFGE patterns that differed by <3 bands were defined as 1 PFGE type; isolates with the same PFGE patterns indicated indistinguishable strains, and those with 2 or 3 different bands indicated closely related strains (15 ).
Similar(53)
The uncertainty in the relative timing between ULF wave bands is defined as the summation of each individual ULF wave band uncertainty.
The volume fraction of the light-colored bands was defined as the area ratio of white pixels, and was regarded as the degree of development of the flow structure for the specimen.
The intensity of NADH spectral band and the intensity of FAD spectral band were defined as A and B, respectively.
Thereafter, each 20 bp interval below and above the median band were defined as representing a distinct genotype [ 27].
The modified elliptical aperture and modified elliptical background aperture for each source and science energy band are defined as the areas of intersection of the elliptical aperture and elliptical background aperture for that source with the field of view, excluding any overlapping source regions.
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