CImbinator

CImbinator analyzes drug combination effects and quantifies synergy to identify and characterize synergistic interactions from small-scale and high-throughput drug combination screens.


Key Features:

  • Batch-Wise Analysis: Supports batch-wise processing to analyze large-scale and high-throughput drug combination datasets.
  • Dataset Scale Support: Handles both small-scale experimental datasets and large-scale/high-throughput screening data.
  • Median Effect Equation: Implements the median effect equation to assess and quantify synergistic or antagonistic interactions.
  • Dose-Response Modeling: Applies advanced experimental mathematical models based on dose-response relationships to quantify drug interactions.
  • R and Ruby Integration: Implemented in Ruby and leverages R for computations, including the R package drc (Dose-Response Curve) for dose-response modeling.

Scientific Applications:

  • Pharmacology and Bioinformatics: Enables analysis of drug interactions to support development and evaluation of combination therapies.
  • Identification of Synergistic Combinations: Identifies potential synergistic drug combinations that may improve therapeutic outcomes.
  • High-Throughput Screening Analysis: Analyzes complex datasets from high-throughput drug combination screens to detect interaction effects.
  • Precision Drug Response Modeling: Enhances precision of drug response modeling through use of advanced mathematical and dose-response approaches.

Methodology:

Computational methods explicitly include the median effect equation, dose-response modeling using the R package drc (Dose-Response Curve), and batch-wise processing implemented in Ruby with R for computations.

Topics

Details

Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
6/6/2018
Last Updated:
11/25/2024

Operations

Publications

Flobak Å, Vazquez M, Lægreid A, Valencia A. CImbinator: a web-based tool for drug synergy analysis in small- and large-scale datasets. Bioinformatics. 2017;33(15):2410-2412. doi:10.1093/bioinformatics/btx161. PMID:28444126. PMCID:PMC5860113.

Documentation