LINPS

LINPS provides pre-computed perturbation profiles of causal biological networks derived from drug-induced gene expression changes from the Library of Integrated Cellular Signatures across cancer cell lines.


Key Features:

  • Data Integration and Pre-computation: Integrates large-scale drug perturbation gene expression datasets from the Library of Integrated Cellular Signatures and converts them into structured representations for downstream analysis.
  • Network Perturbation Amplitudes Analysis: Applies network perturbation amplitudes analysis to quantify how drug treatments alter causal biological networks (CBNs).
  • Cancer-cell Specific Profiles: Provides perturbation profiles specific to cancer cell lines, mapping drug-induced gene expression changes onto CBNs relevant to cancer biology.

Scientific Applications:

  • Therapeutic Target Identification: Facilitates identification of candidate therapeutic targets by revealing nodes and pathways in CBNs affected by drug perturbations.
  • Mechanistic Interpretation of Drug Effects: Enables mechanistic interpretation of drug effects at the network level using drug-induced gene expression changes.
  • Prioritization of Treatment Strategies: Supports prioritization of drug repurposing or combination strategies by comparing perturbation amplitudes across CBNs in cancer cell lines.

Methodology:

Converts LINCS drug perturbation gene expression datasets into structured representations of causal biological networks, pre-computes perturbation profiles across cancer cell lines, and quantifies impacts using network perturbation amplitudes analysis.

Topics

Details

License:
GPL-3.0
Cost:
Free of charge
Tool Type:
command-line tool, web application
Operating Systems:
Mac, Linux, Windows
Programming Languages:
R, Shell
Added:
1/14/2022
Last Updated:
1/14/2022

Operations

Publications

Ahmed M, Kim DR. LINPS: a database for cancer-cell-specific perturbations of biological networks. Database. 2021;2021. doi:10.1093/database/baab048. PMID:34415996. PMCID:PMC8378515.

PMID: 34415996
PMCID: PMC8378515
Funding: - National Research Foundation of Korea grant: 2015R1A5A2008833

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