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Yannis Almirantis

Publications and source records attributed to Yannis Almirantis.

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Multistable Synaptic Plasticity induces Memory Effects and Cohabitation of Chimera and Bump States in Leaky Integrate-and-Fire Networks

Chimera states and bump states are collective synchronization phenomena observed independently (at different parameter regions) in networks of coupled nonlinear oscillators. And while chimera states are characterized by coexistence of coherent and incoherent domains, bump states consist of active domains operating on a silent background. Multistable plasticity in the network connections originates from brain dynamics and is based on the idea that neural cells may transmit inhibitory or excitatory signals depending on various factors, such as local connectivity, influence of neighboring cells etc. During the system/network integration, the link weights adapt and, in the case of multistability, they may organize in coexisting excitatory and/or inhibitory domains. Here, we explore the influence of bistable plasticity on collective synchronization states and we numerically demonstrate that the dynamics of the linking may give rise to co-existence of bump-like and chimera-like states simultaneously in the network. In the case of bump and chimera co-existence, confinement effects are developed: the different domains stay localized and do not travel around the network. Memory effects are also reported in the sense that the final spatial arrangement of the coupling strengths reflects some of the local properties of the initial link distribution. For the quantification of the system's spatial and temporal features, the global and local entropy functions are employed as measures of the network organization, while the average firing rates account for the network evolution and dynamics.

nlin.CD

Extending 1089 attractor to any number of digits and any number of steps

The well-known 1089 trick reflects an amazing trait of digital reversal process and reminisces of a limiting attractor in dynamical systems even though it takes only two steps. It is natural to consider the situations when the number of digits is beyond three as in the original 1089 trick, as well as situations when the number of steps is beyond two. The first part has been mostly done by Webster which we will reproduce. After two steps, the resulting integers are called Papadakis-Webster integers (PWI), which is always divisible by 99, and the resulting quotients consist of only 0's and 1's, which we name Papadakis-Webster binary strings (PWBS). Not all binary strings could be PWBS, and we define the hairpin pairing rule to determine if a binary string is a PWBS. For the second part, we propose a two-option iteration system named iterative digital reversal (IDR) suitably interweaving additions and subtractions. The simplest limiting behavior of IDR is 2-cycles. The elements in an IDR 2-cycle are all composed of repetitions of the 10(9)$_L$89 (L>=0) motif, and are all PWIs. The lower 2-cycle elements after division of 99 belong to the subset of PWBS that are palindromic and consist of 0- and 1-blocks with a minimal length of two. IDR also has higher p-cycles (p=10,12,71) whose elements seem to contain at least one PWI. Another interesting finding about IDR is that it contains non-periodic and diverging trajectories, as the integer values grow to infinity. In these diverging trajectories, while the number of flanking digits around the middle point increases by the iteration, the middle part has an 8-cycle rhythm or signature which has been found in all diverging trajectories. Overall, the generalization of the original 1089 trick in both space and time leads to new patterns in integers and new phenomenology in dynamics.

nlin.CD

Rich dynamical behaviors from a digital reversal operation

Repeatedly adding or subtracting the digital reversal to or from an integer, depending on which one is larger, can be treated as a dynamical system. On one hand, a three-digit version of this map running only two steps is the 1089 mathematical trick problem; on the other hand, this mapping can be compared to John Conway's reverse-add-then-sort (RATS) iteration, as well as the 3x+1 problem, also known as Collatz's map. We numerically run this map and find interesting dynamics, including limiting cycles with unusual periodicity and length-8 diverging trajectories.

nlin.CD

Range-Limited Heaps' Law for Functional DNA Words in the Human Genome

Heaps' or Herdan's law is a linguistic law describing the relationship between the vocabulary/dictionary size (type) and word counts (token) to be a power-law function. Its existence in genomes with certain definition of DNA words is unclear partly because the dictionary size in genome could be much smaller than that in a human language. We define a DNA word as a coding region in a genome that codes for a protein domain. Using human chromosomes and chromosome arms as individual samples, we establish the existence of Heaps' law in the human genome within limited range. Our definition of words in a genomic or proteomic context is different from other definitions such as over-represented k-mers which are much shorter in length. Although an approximate power-law distribution of protein domain sizes due to gene duplication and the related Zipf's law is well known, their translation to the Heaps' law in DNA words is not automatic. Several other animal genomes are shown herein also to exhibit range-limited Heaps' law with our definition of DNA words, though with various exponents. When tokens were randomly sampled and sample sizes reach to the maximum level, a deviation from the Heaps' law was observed, but a quadratic regression in log-log type-token plot fits the data perfectly. Investigation of type-token plot and its regression coefficients could provide an alternative narrative of reusage and redundancy of protein domains as well as creation of new protein domains from a linguistic perspective.

q-bio.GN

Revisiting the Neutral Dynamics Derived Limiting Guanine-Cytosine Content Using the Human De Novo Point Mutation Data

We revisit the topic of human genome guanine-cytosine content under neutral evolution. For this study, the de novo mutation data within human is used to estimate mutational rate instead of using base substitution data between related species. We then define a new measure of mutation bias which separate the de novo mutation counts from the background guanine-cytosine content itself, making comparison between different datasets easier. We derive a new formula for calculating limiting guanine-cytosine content by separating CpG-involved mutational events as an independent variable. Using the formula when CpG-involved mutations are considered, the guanine-cytosine content drops less severely in the limit of neutral dynamics. We provide evidence, under certain assumptions, that an isochore-like structure might remain as a limiting configuration of the neutral mutational dynamics.

q-bio.GN

Optimal Computation of Overabundant Words

The observed frequency of the longest proper prefix, the longest proper suffix, and the longest infix of a word $w$ in a given sequence $x$ can be used for classifying $w$ as avoided or overabundant. The definitions used for the expectation and deviation of $w$ in this statistical model were described and biologically justified by Brendel et al. (J Biomol Struct Dyn 1986). We have very recently introduced a time-optimal algorithm for computing all avoided words of a given sequence over an integer alphabet (Algorithms Mol Biol 2017). In this article, we extend this study by presenting an $\mathcal{O}(n)$-time and $\mathcal{O}(n)$-space algorithm for computing all overabundant words in a sequence $x$ of length $n$ over an integer alphabet. Our main result is based on a new non-trivial combinatorial property of the suffix tree $\mathcal{T}$ of $x$: the number of distinct factors of $x$ whose longest infix is the label of an explicit node of $\mathcal{T}$ is no more than $3n-4$. We further show that the presented algorithm is time-optimal by proving that $\mathcal{O}(n)$ is a tight upper bound for the number of overabundant words. Finally, we present experimental results, using both synthetic and real data, which justify the effectiveness and efficiency of our approach in practical terms.

cs.DS

Optimal Computation of Avoided Words

The deviation of the observed frequency of a word $w$ from its expected frequency in a given sequence $x$ is used to determine whether or not the word is avoided. This concept is particularly useful in DNA linguistic analysis. The value of the standard deviation of $w$, denoted by $std(w)$, effectively characterises the extent of a word by its edge contrast in the context in which it occurs. A word $w$ of length $k>2$ is a $ρ$-avoided word in $x$ if $std(w) \leq ρ$, for a given threshold $ρ< 0$. Notice that such a word may be completely absent from $x$. Hence computing all such words na\"ıvely can be a very time-consuming procedure, in particular for large $k$. In this article, we propose an $O(n)$-time and $O(n)$-space algorithm to compute all $ρ$-avoided words of length $k$ in a given sequence $x$ of length $n$ over a fixed-sized alphabet. We also present a time-optimal $O(σn)$-time and $O(σn)$-space algorithm to compute all $ρ$-avoided words (of any length) in a sequence of length $n$ over an alphabet of size $σ$. Furthermore, we provide a tight asymptotic upper bound for the number of $ρ$-avoided words and the expected length of the longest one. We make available an open-source implementation of our algorithm. Experimental results, using both real and synthetic data, show the efficiency of our implementation.

cs.DS