Related papers: Characterization of Knots and Links Arising From S…
We produce embeddings of knots in thin position that admit compressible thin levels. We also find the bridge number of tangle sums where each tangle is high distance.
We define a family of link concordance invariants $\left\{ s_n \right\}_{n=2,3, \cdots}$. These link concordance invariants give lower bounds on the slice genus of a link $L$. We compute the slice genus of positive links. Moreover, these…
Twisted torus knots and links are given by twisting adjacent strands of a torus link. They are geometrically simple and contain many examples of the smallest volume hyperbolic knots. Many are also Lorenz links. We study the geometry of…
We characterise positive braid links with positive Seifert form via a finite number of forbidden minors. From this we deduce a one-to-one correspondence between prime positive braid links with positive Seifert form and simply laced Dynkin…
We define a knot to be half ribbon if it is the cross-section of a ribbon 2-knot, and observe that ribbon implies half ribbon implies slice. We introduce the half ribbon genus of a knot K, the minimum genus of a ribbon knotted surface of…
We introduce and study knots and links in 2-dimensional complexes. In particular, we define linking numbers for oriented two-component links in 2-complexes and a Kauffman-type bracket polynomial for links in 2-complexes. We also discuss…
Knots and links represent a fundamental motif of non-local connectivity that permeates the physical sciences from string theory to protein folds. While spectral braiding has been explored in two-band non-Hermitian models across various…
Twisted torus links $T(p,q;r,s)$ generalize torus links by introducing $s$ additional twists on $r$ adjacent strands of the torus link $T(p,q)$. It is well known that the number of components of a torus link $T(p, q)$ is given by the…
Phylogenetic networks have gained prominence over the years due to their ability to represent complex non-treelike evolutionary events such as recombination or hybridization. Popular combinatorial objects used to construct them are triplet…
We relate the stability of knot invariants under twisting a pair of strands to the stability of symmetric quivers under unlinking (or linking) operation. Starting from the HOMFLY-PT skein relations, we confirm the stable growth of…
Using Kirby Calculus, we explicitly pass from Berge's R-R descriptions of ten families of knots with lens space surgeries to surgery descriptions on the minimally twisted five chain link (MT5C). Since the MT5C admits a strong involution, we…
Decomposing knots and links into tangles is a useful technique for understanding their properties. The notion of prime tangles was introduced by Kirby and Lickorish in [3]; Lickorish proved [5] that by summing prime tangles one obtains a…
The contents of this 6-page paper have been subsumed into the 13-page paper, "A note on closed 3-braids", arXiv:0802.1072 [math.GT]. This paper is correct, but contains less information than the new one. The topological classification of…
We consider braids with repeating patterns inside arbitrary knots which provides a multi-parametric family of knots, depending on the "evolution" parameter, which controls the number of repetitions. The dependence of knot (super)polynomials…
In this note, we prove a lower bound for the positive kinkiness of a closed braid which we then use to derive an estimate for the positive kinkiness of a link in terms of its Seifert system. As an application, we show that certain pretzel…
Proteins are linear molecular chains that often fold to function. The topology of folding is widely believed to define its properties and function, and knot theory has been applied to study protein structure and its implications. More that…
We provide three 3-dimensional characterizations of the Z-slice genus of a knot, the minimal genus of a locally-flat surface in 4-space cobounding the knot whose complement has cyclic fundamental group: in terms of balanced algebraic…
Disordered networks of semiflexible filaments are common support structures in biology. Familiar examples include fibrous matrices in blood clots, bacterial biofilms, and essential components of cells and tissues of plants, animals, and…
We present four models for a random graph and show that, in each case, the probability that a graph is intrinsically knotted goes to one as the number of vertices increases. We also argue that, for $k \geq 18$, most graphs of order $k$ are…
A knot K is called n-adjacent to another knot K', if K admits a projection containing n generalized crossings such that changing any 0 < m \leq n of them yields a projection of K'. We apply techniques from the theory of sutured 3-manifolds,…