Mahmoud Ahmed

Postdoc - Cancer Genomics

LINPS: a database for cancer-cell-specific perturbations of biological networks


Journal article


Mahmoud Ahmed, Deok Ryong Kim
Database, issue 2021, 2021


View PDF PubMed
Cite

Cite

APA   Click to copy
Ahmed, M., & Kim, D. R. (2021). LINPS: a database for cancer-cell-specific perturbations of biological networks. Database, (2021). https://doi.org/10.1093/database/baab048


Chicago/Turabian   Click to copy
Ahmed, Mahmoud, and Deok Ryong Kim. “LINPS: a Database for Cancer-Cell-Specific Perturbations of Biological Networks.” Database, no. 2021 (2021).


MLA   Click to copy
Ahmed, Mahmoud, and Deok Ryong Kim. “LINPS: a Database for Cancer-Cell-Specific Perturbations of Biological Networks.” Database, no. 2021, 2021, doi:10.1093/database/baab048.


BibTeX   Click to copy

@article{mahmoud2021a,
  title = {LINPS: a database for cancer-cell-specific perturbations of biological networks},
  year = {2021},
  issue = {2021},
  journal = {Database},
  doi = {10.1093/database/baab048},
  author = {Ahmed, Mahmoud and Kim, Deok Ryong}
}

Abstract

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. We used the Library of Integrated Cellular Signatures to model the cell-specific effect of hundreds of drug treatments on gene expression. These signatures were then used to predict the effect of the treatments on several CBN using the network perturbation amplitudes analysis. We packaged the pre-computed scores in a database with an interactive web interface. The intuitive user-friendly interface can be used to query the database for drug perturbations and quantify their effect on multiple key biological functions in cancer cell lines. In addition to describing the process of building the database and the interface, we provide a realistic use case to explain how to use and interpret the results. To sum, 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. Database URL https://bcmslab.shinyapps.io/LINPSAPP/.