[BBC] ISCB Academy tutorial

[Venkata Pardhasaradhi SATAGOPAM]

ISCB Academy is part of the International Society for Computational Biology (ISCB), which aims to provide training and workshops worldwide. We provide hands-on experience accessing and using newly developed bioinformatics tools while ensuring best practices for rigour and reproducibility. The next tutorial is under the title “Integrating gene expression and biological knowledge for drug discovery and repurposing”, which will be held on the 22nd of April at 8:00am EDT.

Description of the Tutorial:

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.

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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.
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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.

Pre-requisites:
● Knowledge of the mechanisms of transcriptional regulation
● Familiarity with high-throughput gene expression data
● Basic knowledge of R and Bioconductor
● Familiarity with Docker and Git (This is only required to execute the code on a local machine)
Register 👉 https://www.iscb.org/iscbacademy

—
Dr. Venkata Satagopam
Bioinformatics Core
Luxembourg Centre For Systems Biomedicine (LCSB)
University of Luxembourg
Campus Belval, House of Biomedicine II
6, avenue du Swing
L-4367 Belvaux

T +352-466-644-6421
F +352-466-644-36421
venkata.satagopam at uni.lu<mailto:venkata.satagopam at uni.lu>
http://lcsb.uni.lu

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