kaleidocell.files

kaleidocell.files

alias of Bundled files available in kaleidocell ======================================== h.all.v2026.1.Hs.symbols.gmt [✓] MSigDB Hallmark gene sets (v2026.1, Human). 50 coherent gene sets representing well-defined biological states and processes, curated to reduce redundancy across MSigDB. Source: https://www.gsea-msigdb.org/gsea/msigdb/. c5.go.bp.v2026.1.Hs.symbols.gmt [✓] MSigDB C5 GO Biological Process gene sets (v2026.1, Human). Gene sets derived from Gene Ontology (GO) biological process terms. Source: https://www.gsea-msigdb.org/gsea/msigdb/. c5.go.cc.v2026.1.Hs.symbols.gmt [✓] MSigDB C5 GO Cellular Component gene sets (v2026.1, Human). Gene sets derived from Gene Ontology (GO) cellular component terms. Source: https://www.gsea-msigdb.org/gsea/msigdb/. c5.go.mf.v2026.1.Hs.symbols.gmt [✓] MSigDB C5 GO Molecular Function gene sets (v2026.1, Human). Gene sets derived from Gene Ontology (GO) molecular function terms. Source: https://www.gsea-msigdb.org/gsea/msigdb/. c6.all.v2026.1.Hs.symbols.gmt [✓] MSigDB C6 Oncogenic Signatures (v2026.1, Human). Gene sets representing signatures of cellular pathways often dysregulated in cancer (e.g. RAS, MYC, E2F). Source: https://www.gsea-msigdb.org/gsea/msigdb/. c7.all.v2026.1.Hs.symbols.gmt [✓] MSigDB C7 Immunologic Signatures (v2026.1, Human). Gene sets representing cell states and perturbations within the immune system. Source: https://www.gsea-msigdb.org/gsea/msigdb/. c8.all.v2026.1.Hs.symbols.gmt [✓] MSigDB C8 Cell Type Signature gene sets (v2026.1, Human). Gene sets of cell type markers curated from single-cell sequencing studies. Source: https://www.gsea-msigdb.org/gsea/msigdb/. c9.all.v2026.1.Hs.symbols.gmt [✓] MSigDB C9 Cancer Gene sets (v2026.1, Human). Gene sets derived from cancer genomics studies including TCGA and other large-scale profiling efforts. Source: https://www.gsea-msigdb.org/gsea/msigdb/. hgnc_ensembl_translation.txt [✓] HGNC → Ensembl gene ID translation table. Tab-separated file mapping HGNC gene symbols to Ensembl gene IDs (GRCh38). Used internally for gene name normalisation..