In order to compare the efficiency of morphological traits and molecular markers in distinguishing the Consolida species, molecular analysis using nrDNA ITS and cpDNA trnL-trnF with maximum parsimony and Bayesian methods were done in a total of 34 species and forma representing 28 species of Consolida, 6 species of Aconitella, plus two species of Delphinium and two species of Aconitum as out gr...

The desire to infer the evolutionary history of a group of species should be more viable now that a considerable amount of multilocus molecular data is available. However, the current molecular phylogenetic paradigm still reconstructs gene trees to represent the species tree. Further, commonly used methods to combine data, such as the concatenation method, the consensus tree method, or the gene...

The forgotten topological index of a molecular graph $G$ is defined as $F(G)=sum_{vin V(G)}d^{3}(v)$, where $d(u)$ denotes the degree of vertex $u$ in $G$. The first through the sixth smallest forgotten indices among all trees, the first through the third smallest forgotten indices among all connected graph with cyclomatic number $gamma=1,2$, the first through<br /...

One of the most widely known topological index is the Wiener index. The Wiener Index Conjecture states that all positive integer numbers except a finite set are the Wiener indices of some trees. We explore the Wiener indices of the binary trees. We present efficient algorithms for generating the Wiener indices of the binary trees. Based on experiments we strengthen the conjecture for the class ...

Maximum likelihood (ML) is increasingly used as an optimality criterion for selecting evolutionary trees, but finding the global optimum is a hard computational task. Because no general analytic solution is known, numeric techniques such as hill climbing or expectation maximization (EM), are used in order to find optimal parameters for a given tree. So far, analytic solutions were derived only ...