The CRIT framework for identifying cross patterns in systems biology and application to chemogenomics.

摘要

Biological data is often tabular but finding statistically valid connections between entities in a sequence of tables can be problematic--for example, connecting particular entities in a drug property table to gene properties in a second table, using a third table associating genes with drugs. Here we present an approach (CRIT) to find connections such as these and show how it can be applied in a variety of genomic contexts including chemogenomics data.CAS Registry/EC Number/Name of Substance 0 (Transcription Factors).