6. Analysis / Visualization Terms

weight

Definition

In network analysis, weight refers to a numerical value assigned to an edge (connection) between nodes that quantifies the strength, intensity, or importance of their relationship. Weights can represent various biological properties: binding affinity between proteins, correlation strength between gene expression profiles, frequency of metabolic flux, or confidence scores for predicted interactions. Weighted networks provide richer information than unweighted graphs by capturing relationship gradients rather than simple presence/absence. Weight values influence network metrics like shortest paths, centrality calculations, and community detection algorithms, enabling more nuanced biological interpretations and prioritization of functionally significant connections.

Visualize weight in Nodes Bio

Nodes Bio enables researchers to visualize edge weights through variable line thickness, color intensity, or numerical labels on connections. Users can filter networks by weight thresholds to focus on high-confidence interactions, apply weighted centrality algorithms to identify key regulatory hubs, and compare weight distributions across experimental conditions. Weight-based visualization helps prioritize therapeutic targets by highlighting the strongest protein-protein interactions or most correlated gene expression patterns.

Visualization Ideas:

  • Protein-protein interaction networks with binding affinity weights shown as edge thickness
  • Gene co-expression networks with correlation coefficients as weighted edges colored by strength
  • Metabolic pathway networks with flux rates as weights to identify bottleneck reactions
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Example Use Case

A cancer researcher analyzing protein-protein interaction networks assigns weights based on experimental binding affinity data (Kd values). By filtering for edges with weights above 0.7 (strong binding), they reduce a 500-node network to 150 high-confidence interactions, revealing a tightly connected cluster of kinases. Weighted betweenness centrality analysis identifies a previously overlooked adapter protein as a critical hub, suggesting it as a novel drug target. The weight-based approach eliminates weak, potentially artifactual interactions that would have obscured this finding.

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