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CoLlAGe captures subtle anisotropic differences in disease pathologies by measuring entropy of co-occurrences of voxel-level gradient orientations on imaging computed within a local neighborhood.

CoLlAGe is based on the hypothesis that disruption in tissue microarchitecture can be quantified on imaging by measuring the disorder in voxel-wise gradient orientations. CoLlAGe involves assigning every image voxel a ‘disorder value’ associated with the co-occurrence matrix of gradient orientations computed around every voxel.

Details on extraction of CoLlAGe features are included in [1]. After feature extraction, the subsequent distribution or different statistics such as mean, median, variance etc can be computed and used in conjunction with a machine learning classifier to distinguish similar appearing pathologies. The feasibility of CoLlAGe in distinguishing cancer from treatment confounders/benign conditions and characterizing molecular subtypes of cancers has been demonstrated in the context of multiple challenging clinical problems.

Code Documentation


The attributes below represent the public output intended to be available to consumers of this module.

Indices and tables