A random walk-based method to identify driver genes by integrating the subcellular localization and variation frequency into bipartite graph

Table 1 The datasets for each cancer type

The second row is the sample counts for each cancer type. The third row represents the involving driver genes for each cancer type. The Mutated count and Outlying count are the genes number for the constructed bipartite graph. Edges are the total number of the edges for each bipartite graph. Density-degree is the value of practical edges out of total edges

ISSN: 1471-2105