Publications by authors named "Jordan C Rozum"

Cellular automata (CA) are discrete dynamical systems with a prominent place in the history and study of artificial life. Here, we focus on the density classification task (DCT) in which a 1-dimensional lattice of Boolean (on/off) automata must perform a form of rudimentary quorum sensing. Typically, the ring lattice consists of 149 cells (though we consider other sizes as well) that update their state according to their own state and its six nearest neighbors in the previous time step.

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Minimum spanning trees and forests are powerful sparsification techniques that remove cycles from weighted graphs to minimize total edge weight while preserving node reachability, with applications in computer science, network science, and graph theory. Despite their utility and ubiquity, they have several limitations, including that they are only defined for undirected networks, they significantly alter dynamics on networks, and they do not generally preserve important network features such as shortest distances, shortest path distribution, and community structure. In contrast, distance backbones, which are subgraphs formed by all edges that obey a generalized triangle inequality, are well defined in directed and undirected graphs and preserve those and other important network features.

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Complex living systems are thought to exist at the "edge of chaos" separating the ordered dynamics of robust function from the disordered dynamics of rapid environmental adaptation. Here, a deeper inspection of 72 experimentally supported discrete dynamical models of cell processes reveals previously unobserved order on long time scales, suggesting greater rigidity in these systems than was previously conjectured. We find that propagation of internal perturbations is transient in most cases, and that even when large perturbation cascades persist, their phenotypic effects are often minimal.

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Genetic regulatory networks (GRNs) regulate the flow of genetic information from the genome to expressed messenger RNAs (mRNAs) and thus are critical to controlling the phenotypic characteristics of cells. Numerous methods exist for profiling mRNA transcript levels and identifying protein-DNA binding interactions at the genome-wide scale. These enable researchers to determine the structure and output of transcriptional regulatory networks, but uncovering the complete structure and regulatory logic of GRNs remains a challenge.

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Biomolecular network dynamics are thought to operate near the critical boundary between ordered and disordered regimes, where large perturbations to a small set of elements neither die out nor spread on average. A biomolecular automaton (e.g.

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Summary: pystablemotifs is a Python 3 library for analyzing Boolean networks. Its non-heuristic and exhaustive attractor identification algorithm was previously presented in Rozum et al. (2021).

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Article Synopsis
  • The paper explores how techniques like parity inversion and time reversal can uncover complex behaviors from simple rules in stochastic models.* -
  • It introduces a new attractor identification algorithm for Boolean networks, highlighting its ability to analyze large systems and resolve a key question in network scaling.* -
  • The findings reveal an unexpectedly low scaling exponent in critical random Boolean networks, suggesting that a system's relation to time reversal influences the range of behaviors it can exhibit.*
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Article Synopsis
  • The authors introduce a technique for identifying control-robust subsets within an interacting system, termed "stable modules," defined by specific constraints on their variables that remain valid over time unless externally altered.
  • Using graph structures to represent causal links between these constraints, stable modules serve as decision points within a system's dynamics, which can be combined to understand complex behavior patterns.
  • The technique is validated through applications to two biological networks, illustrating its utility by predicting cell fates in Drosophila and examining signaling elements in T-cell responses.
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We consider a dynamic framework frequently used to model gene regulatory and signal transduction networks: monotonic ODEs that are composed of Hill functions. We derive conditions under which activity or inactivity in one system variable induces and sustains activity or inactivity in another. Cycles of such influences correspond to positive feedback loops that are self-sustaining and control-robust, in the sense that these feedback loops "trap" the system in a region of state space from which it cannot exit, even if the other system variables are externally controlled.

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