MaxLink
MaxLink identifies and ranks genes closely associated with a user-provided query gene list using a guilt-by-association approach within protein interaction networks to predict potential disease-related genes.
Key Features:
- Guilt-by-association analysis: Infers candidate genes based on association patterns with query genes within protein interaction networks.
- Underlying network: Uses FunCoup 3.0 as the protein interaction network foundation for linkage and association data.
- Gene ranking by connectivity: Produces ranked lists of genes by their connectivity to known disease-associated or query genes.
- Updated algorithm: Incorporates an updated algorithm intended to enhance prediction of potential disease-related genes.
- Statistically robust candidate selection: Adopts a more statistically robust method for selecting candidate genes.
- C++ implementation and performance: Algorithm re-implemented in C++ to improve computational efficiency and speed, facilitating large-scale network analyses.
Scientific Applications:
- Disease gene discovery: Prioritizes candidate genes connected to known disease genes to support identification of novel gene-disease associations.
- Cancer research: Applies guilt-by-association ranking to gene lists in oncology-focused studies.
- General network biology: Enables exploration of gene connections across diverse biological contexts beyond oncology.
Methodology:
Uses a guilt-by-association approach within protein interaction networks (FunCoup 3.0); applies an updated algorithm with a statistically robust method for selecting candidate genes; ranks genes by connectivity to known disease-associated genes; implementation re-implemented in C++ for improved efficiency.
Topics
Details
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- C++, Perl
- Added:
- 8/3/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Guala D, Sjölund E, Sonnhammer ELL. MaxLink: network-based prioritization of genes tightly linked to a disease seed set. Bioinformatics. 2014;30(18):2689-2690. doi:10.1093/bioinformatics/btu344. PMID:24849579.