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Titlebook: Biological Networks and Pathway Analysis; Tatiana V. Tatarinova,Yuri Nikolsky Book 2017 Springer Science+Business Media LLC 2017 Protein-p

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樓主: Daguerreotype
31#
發(fā)表于 2025-3-26 22:34:07 | 只看該作者
Semantic Data Integration and Knowledge Management to Represent Biological Network Associations,as a typical example to illustrate this approach. In this chapter we introduce techniques and concepts (such as ontologies, semantic objects, typed relationships, contexts, graphs, and information layers) that are used to represent complex biomedical networks. The BioXM? Knowledge Management Environ
32#
發(fā)表于 2025-3-27 04:08:24 | 只看該作者
Knowledge-Based Compact Disease Models: A Rapid Path from High-Throughput Data to Understanding Caut tool. The resulting subnetworks provided the basis for generating mechanistic hypotheses that were partially validated by mined experimental evidence. This approach differs from previous consistency-based studies in that the cutoff on the Receiver Operating Characteristic of the true–false separat
33#
發(fā)表于 2025-3-27 05:22:28 | 只看該作者
Functional Network Disruptions in Schizophrenia,of the topological and spatial structure of functional MRI networks in schizophrenia (a) cannot be explained by a disruption to area-based task-dependent responses, i.e., indeed relates to the emergent properties, (b) is global in nature, affecting most dramatically long-distance correlations, and (
34#
發(fā)表于 2025-3-27 10:52:28 | 只看該作者
35#
發(fā)表于 2025-3-27 13:58:55 | 只看該作者
https://doi.org/10.1007/978-3-476-02897-6 the relative importance for each gene product in a molecular pathway remains unclear unless one call for the methods of parameter sensitivity/stiffness analysis in the interactomic kinetic models of signaling pathway activation in terms of total concentrations of each gene product..Here we show two
36#
發(fā)表于 2025-3-27 21:26:08 | 只看該作者
Das Vorbild im Nachbild des Terrorsct of micro RNAs (miRs) on the regulation of cellular interactome. Many alternative sources provide information about miRs and their targets. However, instruments elucidating higher level impact of the established total miR profiles are still largely missing. A variant of OncoFinder termed MiRImpact
37#
發(fā)表于 2025-3-27 23:42:07 | 只看該作者
38#
發(fā)表于 2025-3-28 05:01:38 | 只看該作者
https://doi.org/10.1007/978-3-476-02898-3ncludes tools for gene/protein list enrichment analysis, statistical “interactome” tool for the identification of over- and under-connected proteins in the dataset, and a biological network analysis module made up of network generation algorithms and filters. The suite also features Advanced Search,
39#
發(fā)表于 2025-3-28 08:24:32 | 只看該作者
Kleist Zwischen Aufkl?rung und Romantikof gene sets between two phenotypes. We also present comparative power analysis and Type I error rates for different approaches in each major type of GSA on simulated data. Our evaluation presents a concise guideline for selecting GSA approaches best performing under particular experimental settings
40#
發(fā)表于 2025-3-28 11:29:44 | 只看該作者
https://doi.org/10.1007/978-3-476-02898-3scriptomics and epigenomics data in cancer. The results of this analysis helped us to better understand the molecular mechanisms of cancer development and cancer drug resistance. Such an approach promises to be very effective for rapid and accurate identification of cancer drug targets with true pot
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