Gowinda

Gowinda performs unbiased gene set enrichment analysis for genome-wide association (GWA) studies by correcting sampling biases arising from single-nucleotide polymorphism (SNP) density, gene length, and gene overlap.


Key Features:

  • Permutation tests: Uses permutation-based testing to correct for non-independence and unequal sampling probabilities of genes in GWA studies.
  • Bias correction for gene length and overlap: Accounts for increased SNP counts in longer genes and clustering of overlapping genes during sampling.
  • Gene Ontology (GO) focus: Targets Gene Ontology term enrichment while reducing artifacts specific to SNP-based mappings.
  • False-positive reduction: Reduces the occurrence of false-positive GO terms resulting from unequal gene sampling.
  • Statistical power: Maintains sufficient power to detect genuine enrichments despite bias corrections.
  • Scalability: Employs multi-threading to perform millions of permutations for large datasets.
  • Implementation: Implemented in Java 1.6.

Scientific Applications:

  • GWA gene set enrichment: Analysis of gene set enrichment in genome-wide association (GWA) study results derived from SNP data.
  • GO term interpretation: Identifying genuinely enriched Gene Ontology terms while minimizing bias-driven artifacts.
  • Genetic association interpretation: Supporting interpretation of associations between genetic variation and phenotypic traits, complex biological processes, and disease mechanisms.

Methodology:

Performs permutation tests to correct for unequal gene sampling and non-independence, uses multi-threaded execution to run millions of permutations, and is implemented in Java 1.6.

Topics

Details

License:
MPL-2.0
Maturity:
Mature
Tool Type:
database
Operating Systems:
Linux, Windows, Mac
Programming Languages:
Java
Added:
1/13/2017
Last Updated:
11/25/2024

Operations

Publications

Kofler R, Schlötterer C. Gowinda: unbiased analysis of gene set enrichment for genome-wide association studies. Bioinformatics. 2012;28(15):2084-2085. doi:10.1093/bioinformatics/bts315. PMID:22635606. PMCID:PMC3400962.

Documentation