Omics Integration

RNA-seq Analysis

Upload DESeq2, edgeR, or limma results. GaiaLab extracts your significant genes and runs the full biomedical intelligence pipeline β€” pathways, drugs, hypotheses, and survival β€” automatically.

DESeq2 .csv edgeR .tsv limma .txt .rnk Seurat avg_log2FC

Upload expression results

Accepts any CSV/TSV with gene symbols, log2 fold-change, and adjusted p-value columns. Column names are detected automatically.

πŸ“‚
Drop your file here or click to browse
.csv Β· .tsv Β· .txt Β· .rnk β€” max 50 MB

Significant genes

Genelogβ‚‚FCpadjDirection
Submitting genes to GaiaLab…
This takes 30–60 seconds on first run.

How it works

1
Upload results
Drop any DESeq2, edgeR, or limma output. Column names are detected automatically.
2
Filter DEGs
Set your logFC and padj thresholds. Preview the significant gene list before submitting.
3
Full analysis
GaiaLab runs 54 database queries β€” pathways, drugs, hypotheses, survival β€” on your DEG list.
4
RNA-seq overlay
Results include your expression direction context β€” upregulated vs. downregulated gene annotations.

Expected column names (auto-detected)

Gene symbol
gene Β· gene_name Β· gene_symbol Β· Hugo_Symbol Β· hgnc_symbol Β· external_gene_name
Logβ‚‚ fold-change
log2FoldChange Β· logFC Β· avg_log2FC Β· log2fc Β· LFC
Adjusted p-value
padj Β· adj.P.Val Β· FDR Β· q_value Β· p.adjust Β· BH