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1.
Adv Exp Med Biol ; 936: 225-246, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27739051

RESUMEN

Tumors cannot be understood in isolation from their microenvironment. Tumor and stromal cells change phenotype based upon biochemical and biophysical inputs from their surroundings, even as they interact with and remodel the microenvironment. Cancer should be investigated as an adaptive, multicellular system in a dynamical microenvironment. Computational modeling offers the potential to detangle this complex system, but the modeling platform must ideally account for tumor heterogeneity, substrate and signaling factor biotransport, cell and tissue biophysics, tissue and vascular remodeling, microvascular and interstitial flow, and links between all these sub-systems. Such a platform should leverage high-throughput experimental data, while using open data standards for reproducibility. In this chapter, we review advances by our groups in these key areas, particularly in advanced models of tissue mechanics and interstitial flow, open source simulation software, high-throughput phenotypic screening, and multicellular data standards. In the future, we expect a transformation of computational cancer biology from individual groups modeling isolated parts of cancer, to coalitions of groups combining compatible tools to simulate the 3-D multicellular systems biology of cancer tissues.


Asunto(s)
Líquido Extracelular/diagnóstico por imagen , Modelos Biológicos , Neoplasias/diagnóstico por imagen , Neovascularización Patológica/diagnóstico por imagen , Biología de Sistemas/métodos , Remodelación Vascular , Simulación por Computador , Células Endoteliales/patología , Células Endoteliales/ultraestructura , Hemodinámica , Humanos , Imagenología Tridimensional/estadística & datos numéricos , Neoplasias/irrigación sanguínea , Neoplasias/patología , Neoplasias/ultraestructura , Neovascularización Patológica/patología , Reproducibilidad de los Resultados , Programas Informáticos , Microambiente Tumoral
2.
Sci Rep ; 13(1): 17948, 2023 Oct 20.
Artículo en Inglés | MEDLINE | ID: mdl-37864007

RESUMEN

Deciphering the non-trivial interactions and mechanisms driving the evolution of time-varying complex networks (TVCNs) plays a crucial role in designing optimal control strategies for such networks or enhancing their causal predictive capabilities. In this paper, we advance the science of TVCNs by providing a mathematical framework through which we can gauge how local changes within a complex weighted network affect its global properties. More precisely, we focus on unraveling unknown geometric properties of a network and determine its implications on detecting phase transitions within the dynamics of a TVCN. In this vein, we aim at elaborating a novel and unified approach that can be used to depict the relationship between local interactions in a complex network and its global kinetics. We propose a geometric-inspired framework to characterize the network's state and detect a phase transition between different states, to infer the TVCN's dynamics. A phase of a TVCN is determined by its Forman-Ricci curvature property. Numerical experiments show the usefulness of the proposed curvature formalism to detect the transition between phases within artificially generated networks. Furthermore, we demonstrate the effectiveness of the proposed framework in identifying the phase transition phenomena governing the training and learning processes of artificial neural networks. Moreover, we exploit this approach to investigate the phase transition phenomena in cellular re-programming by interpreting the dynamics of Hi-C matrices as TVCNs and observing singularity trends in the curvature network entropy. Finally, we demonstrate that this curvature formalism can detect a political change. Specifically, our framework can be applied to the US Senate data to detect a political change in the United States of America after the 1994 election, as discussed by political scientists.

3.
Sci Rep ; 12(1): 10883, 2022 06 27.
Artículo en Inglés | MEDLINE | ID: mdl-35760826

RESUMEN

Cellular biological networks represent the molecular interactions that shape function of living cells. Uncovering the organization of a biological network requires efficient and accurate algorithms to determine the components, termed communities, underlying specific processes. Detecting functional communities is challenging because reconstructed biological networks are always incomplete due to technical bias and biological complexity, and the evaluation of putative communities is further complicated by a lack of known ground truth. To address these challenges, we developed a geometric-based detection framework based on Ollivier-Ricci curvature to exploit information about network topology to perform community detection from partially observed biological networks. We further improved this approach by integrating knowledge of gene function, termed side information, into the Ollivier-Ricci curvature algorithm to aid in community detection. This approach identified essential conserved and varied biological communities from partially observed Arabidopsis protein interaction datasets better than the previously used methods. We show that Ollivier-Ricci curvature with side information identified an expanded auxin community to include an important protein stability complex, the Cop9 signalosome, consistent with previous reported links to auxin response and root development. The results show that community detection based on Ollivier-Ricci curvature with side information can uncover novel components and novel communities in biological networks, providing novel insight into the organization and function of complex networks.


Asunto(s)
Algoritmos , Ácidos Indolacéticos
4.
Front Physiol ; 12: 724027, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34925052

RESUMEN

In this paper, a new electromyographic phenomenon, referred to as Bursting Rate Variability (BRV), is reported. Not only does it manifest itself visually as a train of short periods of accrued surface electromyographic (sEMG) activity in the traces, but it has a deeper underpinning because the sEMG bursts are synchronous with wavelet packets in the D8 subband of the Daubechies 3 (db3) wavelet decomposition of the raw signal referred to as "D8 doublets"-which are absent during muscle relaxation. Moreover, the db3 wavelet decomposition reconstructs the entire sEMG bursts with two contiguous relatively high detail coefficients at level 8, suggesting a high incidence of two consecutive neuronal discharges. Most importantly, the timing between successive bursts shows some variability, hence the BRV acronym. Contrary to Heart Rate Variability (HRV), where the R-wave is easily identified, here, time-localization of the burst requires a statistical waveform matching between the "D8 doublet" and the burst in the raw sEMG signal. Furthermore, statistical fitting of the empirical distribution of return times shows a striking difference between control and quadriplegic subjects. Finally, the BRV rate appears to be within 60-88 bursts per minute on average among 9 human subjects, suggesting a possible connection between BRV and HRV.

5.
Sci Rep ; 9(1): 9800, 2019 07 05.
Artículo en Inglés | MEDLINE | ID: mdl-31278341

RESUMEN

Identification of community structures in complex network is of crucial importance for understanding the system's function, organization, robustness and security. Here, we present a novel Ollivier-Ricci curvature (ORC) inspired approach to community identification in complex networks. We demonstrate that the intrinsic geometric underpinning of the ORC offers a natural approach to discover inherent community structures within a network based on interaction among entities. We develop an ORC-based community identification algorithm based on the idea of sequential removal of negatively curved edges symptomatic of high interactions (e.g., traffic, attraction). To illustrate and compare the performance with other community identification methods, we examine the ORC-based algorithm with stochastic block model artificial networks and real-world examples ranging from social to drug-drug interaction networks. The ORC-based algorithm is able to identify communities with either better or comparable performance accuracy and to discover finer hierarchical structures of the network. This opens new geometric avenues for analysis of complex networks dynamics.

6.
Front Physiol ; 9: 1446, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30459629

RESUMEN

Gene expression is a vital process through which cells react to the environment and express functional behavior. Understanding the dynamics of gene expression could prove crucial in unraveling the physical complexities involved in this process. Specifically, understanding the coherent complex structure of transcriptional dynamics is the goal of numerous computational studies aiming to study and finally control cellular processes. Here, we report the scaling properties of gene expression time series in Escherichia coli and Saccharomyces cerevisiae. Unlike previous studies, which report the fractal and long-range dependency of DNA structure, we investigate the individual gene expression dynamics as well as the cross-dependency between them in the context of gene regulatory network. Our results demonstrate that the gene expression time series display fractal and long-range dependence characteristics. In addition, the dynamics between genes and linked transcription factors in gene regulatory networks are also fractal and long-range cross-correlated. The cross-correlation exponents in gene regulatory networks are not unique. The distribution of the cross-correlation exponents of gene regulatory networks for several types of cells can be interpreted as a measure of the complexity of their functional behavior.

7.
Stud Health Technol Inform ; 125: 310-2, 2007.
Artículo en Inglés | MEDLINE | ID: mdl-17377291

RESUMEN

This paper proposes a swarm of magnetically levitated nano-robots with high sensitivity nano-sensors as a mean to detect chemical sources, specifically the chemical signals released by injured nervous cells. In the aftermath of the process, further observation by these nano-robots would be used to monitor the healing process and assess the amount of regeneration, if any, or even the repair, of the injured nervous cells.


Asunto(s)
Diagnóstico por Imagen , Magnetismo , Nanotecnología , Neuronas/patología , Robótica/métodos , Humanos , Imagenología Tridimensional , Estados Unidos
8.
Sci Rep ; 6: 25797, 2016 05 16.
Artículo en Inglés | MEDLINE | ID: mdl-27181056

RESUMEN

Quantum annealing (QA) serves as a specialized optimizer that is able to solve many NP-hard problems and that is believed to have a theoretical advantage over simulated annealing (SA) via quantum tunneling. With the introduction of the D-Wave programmable quantum annealer, a considerable amount of effort has been devoted to detect and quantify quantum speedup. While the debate over speedup remains inconclusive as of now, instead of attempting to show general quantum advantage, here, we focus on a novel real-world application of D-Wave in wireless networking-more specifically, the scheduling of the activation of the air-links for maximum throughput subject to interference avoidance near network nodes. In addition, D-Wave implementation is made error insensitive by a novel Hamiltonian extra penalty weight adjustment that enlarges the gap and substantially reduces the occurrence of interference violations resulting from inevitable spin bias and coupling errors. The major result of this paper is that quantum annealing benefits more than simulated annealing from this gap expansion process, both in terms of ST99 speedup and network queue occupancy. It is the hope that this could become a real-word application niche where potential benefits of quantum annealing could be objectively assessed.

9.
BMC Syst Biol ; 10(1): 92, 2016 Sep 21.
Artículo en Inglés | MEDLINE | ID: mdl-27655224

RESUMEN

BACKGROUND: The increased availability of high-throughput datasets has revealed a need for reproducible and accessible analyses which can quantitatively relate molecular changes to phenotypic behavior. Existing tools for quantitative analysis generally require expert knowledge. RESULTS: CellPD (cell phenotype digitizer) facilitates quantitative phenotype analysis, allowing users to fit mathematical models of cell population dynamics without specialized training. CellPD requires one input (a spreadsheet) and generates multiple outputs including parameter estimation reports, high-quality plots, and minable XML files. We validated CellPD's estimates by comparing it with a previously published tool (cellGrowth) and with Microsoft Excel's built-in functions. CellPD correctly estimates the net growth rate of cell cultures and is more robust to data sparsity than cellGrowth. When we tested CellPD's usability, biologists (without training in computational modeling) ran CellPD correctly on sample data within 30 min. To demonstrate CellPD's ability to aid in the analysis of high throughput data, we created a synthetic high content screening (HCS) data set, where a simulated cell line is exposed to two hypothetical drug compounds at several doses. CellPD correctly estimates the drug-dependent birth, death, and net growth rates. Furthermore, CellPD's estimates quantify and distinguish between the cytostatic and cytotoxic effects of both drugs-analyses that cannot readily be performed with spreadsheet software such as Microsoft Excel or without specialized computational expertise and programming environments. CONCLUSIONS: CellPD is an open source tool that can be used by scientists (with or without a background in computational or mathematical modeling) to quantify key aspects of cell phenotypes (such as cell cycle and death parameters). Early applications of CellPD may include drug effect quantification, functional analysis of gene knockout experiments, data quality control, minable big data generation, and integration of biological data with computational models.

10.
IEEE Trans Neural Netw ; 16(5): 1163-73, 2005 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-16252824

RESUMEN

Buffer management in queuing systems plays an important role in addressing the tradeoff between efficiency measured in terms of overall packet loss and fairness measured in terms of individual source packet loss. Complete partitioning (CP) of a buffer with the best fairness characteristic and complete sharing (CS) of a buffer with the best efficiency characteristic are at the opposite ends of the spectrum of buffer management techniques. Dynamic partitioning buffer management techniques aim at addressing the tradeoff between efficiency and fairness. Ease of implementation is the key issue when determining the practicality of a dynamic buffer management technique. In this paper, two novel dynamic buffer management techniques for queuing systems accommodating self-similar traffic patterns are introduced. The techniques take advantage of the adaptive learning power of perceptron neural networks when applied to arriving traffic patterns of queuing systems. Relying on the water-filling approach, our proposed techniques are capable of coping with the tradeoff between packet loss and fairness issues. Computer simulations reveal that both of the proposed techniques enjoy great efficiency and fairness characteristics as well as ease of implementation.


Asunto(s)
Artefactos , Almacenamiento y Recuperación de la Información/métodos , Internet , Redes Neurales de la Computación , Reconocimiento de Normas Patrones Automatizadas/métodos , Procesamiento de Señales Asistido por Computador , Algoritmos , Inteligencia Artificial , Simulación por Computador , Modelos Estadísticos , Telecomunicaciones
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