Screening for potential cancer therapies using existing large datasets of drug perturbations requires expertise and resources not available to all. This is often a barrier for lab scientists to tap into these valuable resources. To address these issues, one can take advantage of prior knowledge especially those coded in standard formats such as causal biological networks (CBN). Large datasets can be converted into appropriate structures, analyzed once and the results made freely available in easy-to-use formats. In these three parts tutorial, we will give a full description of one large scale analysis of using this approach, one case study of building a network of metastasis suppressors from scratch, and a walkthrough example code to perform and adapt these tools for different use cases.

• Part One: a talk describing the construction of a database for cancer-cell-specific perturbations of biological networks (LINPS). We pre-computed cancer-cell-specific perturbation amplitudes of several biological networks and made the output available in a database with an interactive web interface.
• Part Two: a talk describing the building of a functional network model of the metastasis suppressor RKIP and its regulators in breast cancer cells. In this case study, we applied text mining and a manual literature search to extract known interactions between several metastasis suppressors and their regulators. Then we adopted a reverse causal reasoning approach to evaluate and prioritize pathways that are most consistent and responsive to drugs that inhibit cell growth. We further validated some of the predicted regulatory links in the breast cancer cell line MCF7 experimentally and highlighted the points of uncertainty in our model.

• Part Three: a code walkthrough encoding directed interactions into the biological expression language (BEL), computing the network perturbation amplitudes (NPA), and interpreting the output.