Related papers: Knot Fertility and Lineage
We give a recipe for constructing families of distinct knots that have identical Khovanov homology and give examples of pairs of prime knots, as well as infinite families, with this property.
Knot Theory is currently a very broad field. Even a long survey can only cover a narrow area. Here we concentrate on the path from Goeritz matrices to quasi-alternating links. On the way, we often stray from the main road and tell related…
The genus of knots is a one of the fundamental invariant and can be seen as a complexity of knots. In this paper, we give a lower bound of genus using Dehornoy floor, which is a measure of complexity of braids in terms of braid ordering.
Introduced recently, an n-crossing is a singular point in a projection of a link at which n strands cross such that each strand travels straight through the crossing. We introduce the notion of an \"ubercrossing projection, a knot…
The list of knots with up to 10 crossings is commonly referred to as the Rolfsen Table. This paper presents a way to generate the Rolfsen table in a simple, clear, and reproducible manner. The methods we use are similar to those used by J.…
The knots-quivers correspondence states that various characteristics of a knot are encoded in the corresponding quiver and the moduli space of its representations. However, this correspondence is not a bijection: more than one quiver may be…
The slicing degree of a knot $K$ is defined as the smallest integer $k$ such that $K$ is $k$-slice in $\#^n \overline{\mathbb{CP}^2}$ for some $n$. In this paper, we establish bounds for the slicing degrees of knots using Rasmussen's…
The altenating knots, links and twists projected on the S_2 sphere are identified with the phase Space of a Hamiltonian dynamic system of one degree of freedom. The saddles of the system correspond to the crossing points, the edges, to the…
Roberts proved that a family of alternating, arborescent, prime knots each have at least $2^{2n-1}$ distinct minimal genus Seifert surfaces, where $n$ is the genus of the knot in question. We give a subfamily of these knots that have…
The slicing number of a knot, $u_s(K)$, is the minimum number of crossing changes required to convert $K$ to a slice knot. This invariant is bounded above by the unknotting number and below by the slice genus $g_s(K)$. We show that for many…
Knot theory is actively studied both by physicists and mathematicians as it provides a connecting centerpiece for many physical and mathematical theories. One of the challenging problems in knot theory is distinguishing mutant knots. Mutant…
We introduce new skein invariants of links based on a procedure where we first apply the skein relation only to crossings of distinct components, so as to produce collections of unlinked knots. We then evaluate the resulting knots using a…
Knot Floer homology is a knot invariant defined using holomorphic curves. In more recent work, taking cues from bordered Floer homology,the authors described another knot invariant, called "bordered knot Floer homology", which has an…
In a previous paper (q-alg/9501022) we suggested some algorithms that could be useful in solving the problem of knot classification. Here we continue this discussion by answering questions raised in that paper and by commenting on practical…
In knot concordance three genera arise naturally, g(K), g_4(K), and g_c(K): these are the classical genus, the 4-ball genus, and the concordance genus, defined to be the minimum genus among all knots concordant to K. Clearly 0 <= g_4(K) <=…
This paper introduces a new algebra, the crossing algebra, that is applied to count the number of components for arborescent knots, links, tangles or states (of a state polynomial expansion such as the Kauffman bracket). This algebra is…
The primary objects of study in the ``knot theory of complex plane curves'' are C-links: links (or knots) cut out of a 3-sphere in the complex plane by complex plane transverse and totally tangential. Transverse C-links are naturally…
In this paper, we study a geometric/topological measure of knots and links called the nullification number. The nullification of knots/links is believed to be biologically relevant. For example, in DNA topology, one can intuitively regard…
We derive a linear estimate of the signature of positive knots, in terms of their genus. As an application, we show that every knot concordance class contains at most finitely many positive knots.
We extend knot contact homology to a theory over the ring $\mathbb{Z}[\lambda^{\pm 1},\mu^{\pm 1}]$, with the invariant given topologically and combinatorially. The improved invariant, which is defined for framed knots in $S^3$ and can be…