We investigate a generalization of Hopf algebra $\mathfrak{sl}_{q}\left( 2\right) $ by weakening the invertibility of the generator $K$, i.e. exchanging its invertibility $KK^{-1}=1$ to the regularity $K\overline{K}K=K$. This leads to a weak Hopf algebra $w\mathfrak{sl}_{q}\left( 2\right) $ and a $J$-weak Hopf algebra $v\mathfrak{sl}_{q}\left( 2\right) $ which are studied in detail. It is shown that the monoids of group-like elements of $w\mathfrak{sl}_{q}\left( 2\right) $ and $v\mathfrak{sl}_{q}\left( 2\right) $ are regular monoids, which supports the general conjucture on the connection betweek weak Hopf algebras and regular monoids. Moreover, from $w\mathfrak{sl}_{q}\left( 2\right) $ a quasi-braided weak Hopf algebra $\overline{U}_{q}^{w}$ is constructed and it is shown that the corresponding quasi-$R$-matrix is regular $R^{w}\hat{R}^{w}R^{w}=R^{w}$.

Consider an age-dependent, single-species branching process defined by a progeny number distribution, and a lifetime distribution associated with each independent particle. In this paper, we focus on the associated inverse problem where one wishes to formally solve for the progeny number distribution or the lifetime distribution that defines the Bellman-Harris branching process. We derive results for the existence and uniqueness (the identifiability) of these two distributions given one of two types of information: the extinction time probability of the entire process (extinction time distribution), or the distribution of the total number of particles at one fixed time. We demonstrate that perfect knowledge of the distribution of extinction times allows us to formally determine either the progeny number distribution or the lifetime distribution. Furthermore, we show that these constructions are unique. We then consider “data” consisting of a perfectly known total number distribution given at one specific time. For a process with known progeny number distribution and exponentially distributed lifetimes, we show that the rate parameter is identifiable. For general lifetime distributions, we also show that the progeny distribution is globally unique. Our results are presented through four theorems, each describing the constructions in the four distinct cases.

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.

The dynamic formulation of optimal transport has attracted growing interests in scientific computing and machine learning, and its computation requires to solve a PDE-constrained optimization problem. The classical Eulerian discretization based approaches suffer from the curse of dimensionality, which arises from the approximation of high-dimensional velocity field. In this work, we propose a deep learning based method to solve the dynamic optimal transport in high dimensional space. Our method contains three main ingredients: a carefully designed representation of the velocity field, the discretization of the PDE constraint along the characteristics, and the computation of high dimensional integral by Monte Carlo method in each time step. Specifically, in the representation of the velocity field, we apply the classical nodal basis function in time and the deep neural networks in space domain with the H1-norm regularization. This technique promotes the regularity of the velocity field in both time and space such that the discretization along the characteristic remains to be stable during the training process. Extensive numerical examples have been conducted to test the proposed method. Compared to other solvers of optimal transport, our method could give more accurate results in high dimensional cases and has very good scalability with respect to dimension. Finally, we extend our method to more complicated cases such as crowd motion problem.

Let $\Omega $ be a bounded $C^2$ domain in $R^n$ and $\phi : \partial \Omega \to \mathbb{R}^m$ be a continuous map. The Dirichlet problem for the minimal surface system asks whether there exists a Lipschitz map $f : \Omega \to \mathbb{R}^m$ with $ f |_{\partial \Omega}$ and with the graph of $f$ a minimal submanifold in $R^{n+m}$. For $m = 1$, the Dirichlet problem was solved more than thirty years ago by Jenkins-Serrin [13] for any mean convex domains and the solutions are all smooth. This paper considers the Dirichlet problem for convex domains in arbitrary codimension $m$. We prove if $\psi : \bar{\Omega} \to \mathbb{R}^m$ satisfies $8n\delta sup_{\Omega}||D^2 \psi| + \sqrt{2} sup_{\partial \Omega} |D\psi| <1$, then the Dirichlet problem for $ \psi |_{\partial \Omega}$ is solvable in smooth maps. Here $\delta$ is the diameter of $\Omega$ . Such a condition is necessary in view of an example of Lawson-Osserman [15]. In order to prove this result, we study the associated parabolic system and solve the Cauchy-Dirichlet problem with $\psi$ as initial data.