Project: Library of Integrated Network-based Cellular Signatures
Gene Set Library: RummaGEO DrugPerturbations 2025
Genes: 1,877
Description: A gene set from RummaGEO DrugPerturbations 2025 provided by LINCS
Label | Description |
---|---|
SNF2 related chromatin remodeling ATPase 5 | |
aspartate beta-hydroxylase | |
SUMO peptidase family member, NEDD8 specific | |
keratin 15 | |
cyclin dependent kinase inhibitor 2B | |
sulfiredoxin 1 | |
general transcription factor IIIC subunit 1 | |
cholinergic receptor nicotinic alpha 5 subunit | |
prolyl 3-hydroxylase 1 | |
prostaglandin E synthase 2 |
Perform Gene Set Enrichment with this gene set against Common Fund program's gene sets, identifying significant overlaps using a pre-built PWB workflow. Run the workflow with GSE118548 1 V 2 TRAMETINIB HUMAN UP.
GeneSetCart helps you to fetch gene sets from various data sources, augment, combine with set operations, visualize and analyze these gene sets in a single session. Start a new session with GSE118548 1 V 2 TRAMETINIB HUMAN UP.
CFDE-GSE illuminates connections between the input gene set and various CF gene sets that overlap with the queried gene set. Query CFDE-GSE with GSE118548 1 V 2 TRAMETINIB HUMAN UP.
The Playbook Workflow Builder helps you interactively construct workflows leveraging CFDE APIs without code. Start a new workflow with GSE118548 1 V 2 TRAMETINIB HUMAN UP.