PPI |
Estimate edge biomarkers according to differential expressed genes and protein-protein interactions. |
Classify patients accurately and integrate protein-protein interaction information. |
[50] |
EdgeBiomarker |
Construct an individual specific network through the expression profile of a single sample and integrating the edge and node markers of the biological network. |
Diagnose the phenotype of each individual. |
[42] |
SSN |
Construct individual specific networks based on the molecular expression of a single sample. |
Clarify the molecular mechanisms of complex diseases of each individual at the system level. |
[43] |
P-SSN |
Construct single-sample network and retain the direct interactions by excluding indirect interactions. |
Predict driver mutation genes based on single-sample data, subtype complex diseases and cluster single cells. |
[44] |
TRFBA |
Integrate transcriptional regulatory and metabolic models using a set of expression data for various perturbations. |
Integrate transcriptome and metabolome data and improve the quantitatively prediction of growth rate. |
[45] |
SCS |
Use mutation data and expression data to identify personalized driver mutation profiles from the perspective of network controllability. |
Predict personalized driver mutation spectrum. |
[46] |
CSN |
Construct a cell-specific network (CSN) for each single cell from scRNA-seq data. |
Cluster and pseudo-trajectory at network level; find important non-differential genes. |
[47] |
c-CSN |
Eliminate indirect associations to measure direct associations between genes. |
Resolve the direction of differentiation trajectories by quantifying the potency of each single cell. |
[48] |
NBSBM |
Method of sparse Bayesian machine based on network. |
Predict drug sensitivity and reveal the underlying mechanism of drug action. |
[49] |