Difference between revisions of "Gene set enrichment analysis HumanPSD (Agilent probes) (workflow)"

Latest revision as of 16:34, 12 March 2019

Workflow title

Gene set enrichment analysis HumanPSD (Agilent probes)

Provider

geneXplain GmbH

[edit] Workflow overview

[edit] Description

This workflow is designed to perform Gene Set Enrichment Analysis, GSEA, as it is described at http://www.broadinstitute.org/gsea/index.jsp.  As input, the normalized data with Agilent probeset IDs can be submitted. Such normalized files result from the “Normalize data” procedure under “Analyses/Methods/Data normalization/Normalize Agilent experiment and control”.

First, the input files are subjected to fold-change calculation. The table with probeset IDs and calculated fold change values is converted into a table with Ensembl Gene IDs. In the next step, the Ensembl genes are annotated with additional information, gene descriptions and gene symbols.

Finally the annotated Ensembl genes are subjected to GSEA using the HumanPSD^TM database. Enrichment analysis is performed using the following ontologies: HumanPSD GO biological processes, HumanPSD GO cellular components, HumanPSD GO molecular function, HumanPSD disease and by the TRANSPATH pathways.

Output files include enrichment analysis results, a list of annotated Ensemble genes and a histogram of log fold change distribution. For each ontological term several parameters are calculated, including nominal p-value, ES, NES, FDR, rank at max, hit names, the link to the corresponding ontological term, and the link to open a visualization plot.

[edit] Parameters

Experiment normalized

Control normalized

Annotation source

Species

Results folder