Multi-omics RCD gene set test

Description

omicsRCD is a multivariate pathway enrichment analysis tool that identifies RCD gene sets over-represented in a list or matrix of genes. It combines multiple omics datasets based on a data fusion method, prioritises genes based on the significance of signals from the omics datasets, and performs pathway enrichment analysis of these prioritised genes. It can find active RCD pathways supported by single or multiple omics datasets, as well as those that are only apparent through data integration and remain undetected in any single dataset alone.

New analysis

A data table: a matrix containing p values, with genes as rows and omics values as columns. Please arrange genes in the odd-numbered columns and their corresponding p values in the even-numbered columns. The order and IDs in the odd-numbered columns do not need to be consistent. The tool will handle and resolve any discrepancies automatically.

Please use gene symbols for better performance. See Help for all supported gene IDs.

Gene1Omics1Gene2Omics2
GENEA0.012GENEC0.023
GENEB0.034GENEOTHER0.045
GENEC0.056GENEB0.067
  
Retrieve history results

For a newly submitted analysis, the Analysis ID field below will be automatically populated. Please save this ID for future reference. The results will be retained for 48 hours.

Please do not click the  Get  button during the newly submitted analysis.

  
Output