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Five scale geometry variants are defined (average, anterior, tail, ventral, and pectoral fin) and their functional implications are discussed in terms of the interscale mobility mechanisms that enable flexibility within the exoskeleton.
Variants are defined as peptides with at least one amino acid difference from their corresponding identified epitope.
To be unambiguously identified, genetic variants are defined at the genomic DNA level.
The LND variants are defined by HPRT deficiency without self-injurious behaviour, a hallmark feature of classic LND.
When both risk and protective variants are defined in the simulation runs, our newly introduced measure showed even more power compared with the other methods.
This work led to the construction of a structural haplotype of 59kb across the CNV, in which the relative positions of different gene sequence variants are defined.
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Inactive variants were defined as variants which showed no detectable activity in buffer.
Historically, virus variants were defined by serology; a total lack of cross-reactivity means a different virus type and lack of cross-reactivity of a particular protein defines a subtype.
The immunoreactivity of the PEGylated variants was defined as the ratio of the WT-his EC50 to the EC50 of the corresponding PEGylated enzyme.
The remaining variants were defined as the candidate variants.
"Rare variants" were defined as variants with Minor Allele Frequency (MAF) of less than 1%.
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