We propose an inverse iterative method for computing the Perron pair of an irreducible nonnegative third order tensor. The method involves the selection of a parameter $\theta_k$ in the $k$th iteration. For every positive starting vector, the method converges quadratically and is positivity preserving in the sense that the vectors approximating the Perron vector are strictly positive in each iteration. It is also shown that $\theta_k=1$ near convergence. The computational work for each iteration of the proposed method is less than four times (three times if the tensor is symmetric in modes two and three, and twice if we also take the parameter to be $1$ directly) that for each iteration of the Ng--Qi--Zhou algorithm, which is linearly convergent for essentially positive tensors.

No abstract uploaded!

No abstract uploaded!

In this note we establish some general finiteness results concerning lattices Γ in connected Lie groups$G$which possess certain “density” properties (see$Moskowitz$, M., On the density theorems of Borel and Furstenberg,$Ark. Mat.$$16$(1978), 11–27, and$Moskowitz$, M., Some results on automorphisms of bounded displacement and bounded cocycles,$Monatsh. Math.$$85$(1978), 323–336). For such groups we show that Γ always has finite index in its normalizer$N$_{$G$}(Γ). We then investigate analogous questions for the automorphism group Aut($G$) proving, under appropriate conditions, that Stab_{Aut($G$)}(Γ) is discrete. Finally we show, under appropriate conditions, that the subgroup $\tilde{\Gamma}=\{i_{\gamma}:\gamma \in \Gamma \},\ i_{\gamma}(x)=\gamma x\gamma^{-1}$ , of Aut($G$) has finite index in Stab_{Aut($G$)}(Γ). We test the limits of our results with various examples and counterexamples.

Comparing DNA and protein sequence groups plays an important role in biological evolutionary relationship research. Despite many methods available for sequence comparison, only a few can be used for group comparison. In this study, we propose a novel approach using convex hulls. We use statistical information contained within the sequences to represent each sequence as a point in high dimensional space. We find that the points belonging to one biological group are located in a different region of space than points belonging to other biological groups. To be more precise, the convex hull of the points from one group are disjoint from the convex hulls of points from other groups. This finding allows us to do phylogenetic analysis for groups in an efficient way. Five different theorems are presented for checking whether two convex hulls intersect or are disjoint. Test results for datasets related to HRV, HPV, Ebolavirus, PKC and protein phosphatase domains demonstrate that our method performs well and provides a new tool for studying group phylogeny. More significantly, the convex analysis presents a new way to search for sequences belonging to a biological group by examining points within the group’s convex hull.