Groups comprising many variable sequences sharing low variability were found.
Like Bull et al. [31] with PoLV 1 4 sequences, we used positions of 'limited variability', described as highly variable sequences, to classify DBL6ε sequences.
Moreover, we did not find any country where all variable sequences share low variability and are represented by a single consensus sequence.
The objective of our analysis has been to classify the variable sequences in order to understand how variability is distributed over the DBL6ε domain.
Remark 3.4 Since NOD random variable sequences and NA random variable sequences are the most important and special cases of pairwise NQD random variable sequences, then we have the following results as two corollaries of Theorems 2.1 and 2.2.
Hence, sequences of ANA random variables are a family of very wide scope, which contain NA random variable sequences and ρ̃-mixing random variable sequences.
The C-terminal region has variable sequences, and folds into a conserved amphipathic α-helical structure.
The multiple time-varying stochastic communication delays are introduced via stochastic variable sequences following Bernoulli distribution.
For independent and identically distributed random variable sequences, Jamison et al. [7] proved the following theorem.
When these are compared with the corresponding results of independent random variable sequences, there still remains much to be desired.
Since the amplicons of ORF2/3-137 Pcontainain variable sequences, a phylogenetic tree of the ORF2/3-137 producouldould clearly distinguish the different HEV genotypes.
