Last updated: 2026-07-02
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immgenT-GP-analysis/analysis/
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| html | 06b2461 | Ziang Zhang | 2026-07-02 | Initial commit: immgenT-GP-analysis |
Produced by script-refactor/TableS1.R:
# Supplementary Table 1: per-GP summary.
#
# One row per GP: which Level-1/Level-2/condition/organ categories it
# predicts well (AUC > 0.8, driven by high loading), plus its top positive
# and negative signature genes.
#
# Source: ported from script/Supplement_Table1.R (unchanged apart from the
# output path).
data_path <- "data/"
output_path <- "figure-refactor/"
L_pm_filtered <- readRDS(paste0(data_path, "L_pm_filtered.rds"))
F_pm_filtered <- readRDS(paste0(data_path, "F_pm_filtered.rds"))
level_1_AUC_list <- readRDS(paste0(data_path, "level_1_AUC_list_figure.rds"))
level_2_AUC_list <- readRDS(paste0(data_path, "level_2_AUC_list_figure.rds"))
condition_detailed_AUC_list_figure <- readRDS(paste0(data_path, "condition_detailed_AUC_list_figure.rds"))
organ_simplified_AUC_list_figure <- readRDS(paste0(data_path, "organ_simplified_AUC_list_figure.rds"))
# Normalize F_pm_filtered such that each column has max abs value of 1
F_pm_filtered <- apply(F_pm_filtered, 2, function(x) x / max(abs(x)))
colnames(F_pm_filtered) <- colnames(L_pm_filtered)
gps <- colnames(F_pm_filtered)
get_passing_categories <- function(auc_list, gps, L_mat, threshold = 0.8) {
auc_mat <- auc_list$auc
thr_mat <- auc_list$threshold
gp_median_loading <- apply(L_mat, 2, median)
lapply(gps, function(gp) {
if (!gp %in% colnames(auc_mat)) return("")
auc_vals <- auc_mat[, gp]
thr_vals <- thr_mat[, gp]
med_load <- gp_median_loading[gp]
# Keep only categories predicted by HIGH loading (threshold >= median loading)
cats <- rownames(auc_mat)[auc_vals > threshold & thr_vals >= med_load]
paste(cats, collapse = "; ")
})
}
level1_cats <- get_passing_categories(level_1_AUC_list, gps, L_pm_filtered)
level2_cats <- get_passing_categories(level_2_AUC_list, gps, L_pm_filtered)
condition_cats <- get_passing_categories(condition_detailed_AUC_list_figure, gps, L_pm_filtered)
organ_cats <- get_passing_categories(organ_simplified_AUC_list_figure, gps, L_pm_filtered)
sig_genes_pos <- lapply(gps, function(gp) {
vals <- F_pm_filtered[, gp]
candidates <- names(vals)[vals > 0.25]
top <- head(candidates[order(vals[candidates], decreasing = TRUE)], 5)
paste(top, collapse = "; ")
})
sig_genes_neg <- lapply(gps, function(gp) {
vals <- F_pm_filtered[, gp]
candidates <- names(vals)[vals < -0.25]
top <- head(candidates[order(abs(vals[candidates]), decreasing = TRUE)], 5)
paste(top, collapse = "; ")
})
supp_table <- data.frame(
GP = gps,
Level1 = unlist(level1_cats),
Level2 = unlist(level2_cats),
Condition = unlist(condition_cats),
Organ = unlist(organ_cats),
Signature_Genes_Pos = unlist(sig_genes_pos),
Signature_Genes_Neg = unlist(sig_genes_neg),
stringsAsFactors = FALSE
)
write.csv(supp_table, file = paste0(output_path, "Supplementary_Table1_GP_summary.csv"), row.names = FALSE)Showing the first 20 rows (of 200); download the full table at figure-refactor/Supplementary_Table1_GP_summary.csv.
| GP | Level1 | Level2 | Condition | Organ | Signature_Genes_Pos | Signature_Genes_Neg |
|---|---|---|---|---|---|---|
| K1 | CD8.K; CD4.Y; CD4.P; Treg.P; gdT.B; gdT.C; gdT.D; gdT.P; CD8aa.C; CD8aa.D; CD8aa.P; DP.wY; DP.wP | CT010467.1; Tmsb4x; Actb; Tmsb10; Eef1a1 | ||||
| K2 | CD8.wM; CD4.wM; Treg.wM; gdT.E; gdT.wM; CD8aa.wM; Tz.wM; DN.wM; DP.wC; DP.wM | PDAC_SoyHFD | Arhgap15; Dock2; Mbnl1; Inpp4b; Foxp1 | Tmsb10; Tmsb4x; Fau; Pfn1; Ppia | ||
| K3 | gdT.A; gdT.B; gdT.C; gdT.D; gdT.E; gdT.F; gdT.Z; CD8aa.C; CD8aa.D; CD8aa.E; DP.wY | CeDtg; CeDtg_glia; Ddvillin; Ddvillin_glia; MNVCR6; MNVCW3 | small intestine epi | Gzma; Cd7; Ccl5; Fcer1g; Tyrobp | Tmsb10; Tpt1; CT010467.1; Actb; Tmsb4x | |
| K4 | CD4.wN | SLO | Tmsb10; Fau; CT010467.1; Pfn1; Ppia | Dock2; Rack1; Arhgap15; Myh9; Ptprc | ||
| K5 | CD8.K; CD8.P; CD4.P; Treg.P; gdT.P; CD8aa.P; Tz.P; DN.P; DP.wP | H2ac8; H1f5; H1f4; H4c4; Hist1h2ap | ||||
| K6 | CD4.T; CD4.U; CD4.X; CD4.Y; CD4.P; Treg.D; Treg.E; gdT.Q; gdT.R; gdT.S; gdT.T; gdT.U; gdT.V; gdT.X; gdT.Z; Tz.D | Crodentium; MTB_49w; Saureus | S100a6; Gzmb; Lgals1; Vim; Crip1 | Tmsb10; CT010467.1; Eef1a1; Cmss1; Cdk8 | ||
| K7 | gdT.X; gdT.Z; DP.wG | CT010467.1; Ccl5; Cmss1; Cdk8; Crip1 | Igfbp4; Ccr7; Limd2 | |||
| K8 | gdT.Z | VV_D63_AntigenExperienced; VV_D63_bystander; VV_D80_bystander | Fth1; S100a6; Thy1; Ctla2a; Gem | Ccl5; Gzma; Gzmb; AW112010; Tyrobp | ||
| K9 | CD8.wU; CD8.wV; DP.wC; DP.wD; DP.wE | Cdk8; Cmss1; CT010467.1; Eef2; Myh9 | Tmsb10; Fau; Tmsb4x; Cd52 | |||
| K10 | CD8.G; CD8.H; CD8.I; CD8.J; CD8.K; CD8.wU; CD8.wY; CD4.S; DN.F | dirty_2m_LCMVarm_D30; dirty_2m_LCMVarm_D7; GBMpron; LCMVarm_intravascular; LCMVarm_intravascularcirculating; LCMVarm_intravascularsurveilling | Ccl5; Gzma; Lgals1; Nkg7; Ly6c2 | |||
| K11 | placenta; kidney | Vps37b; Gramd3; Dusp10; Junb; Ccr7 | Cd52; Ltb; Ptprcap | |||
| K12 | CD8.C; CD8.wX; CD4.G; CD4.H; CD4.I; CD4.U; Treg.B; DN.A; DN.G | Izumo1r; Cdk8; Tox; Tbc1d4; Pdcd1 | Crip1; Ccl5; Satb1; Igfbp4; Selplg | |||
| K13 | CD4.X; CD4.Y; gdT.Q; gdT.R; gdT.S; gdT.T; gdT.U; gdT.V; Tz.D | D3; Foxp3mutant_D3; Saureus | Tmem176b; Tmem176a; Il7r; CT010467.1; Cd163l1 | Ms4a4b; Inpp4b; Ctla4; Ifi27l2a; Cd2 | ||
| K14 | DP.wF; DP.wG | Cd8b1; Cd8a; Satb1; Rag1; Themis | H2-K1; Crip1; H2-D1; B2m; Eef1a1 | |||
| K15 | CD8.D; CD8.F; CD4.F; Treg.C; gdT.X; DN.G; DN.H; DP.wH | Eif5a; Npm1; Hsp90ab1; Ncl; Mif | Malat1; Tmsb4x; Itm2b; Cd52; Ypel3 | |||
| K16 | CD8.F; CD4.D; DN.I; DN.J | B16_ACTaPD1a41BB; CtrachomatisL2_primaryD5; LCMVcl13_D8; Toxo_D9 | Ifi27l2a; Isg15; Ly6a; Bst2; Stat1 | |||
| K17 | Ifi27l2a; Atp5e; Tmsb4x; Ripor2; Lef1 | Actg1; Ubb; Hspa8; Eef1a1; Il31ra | ||||
| K18 | Cpa3; CT010467.1; Crip1; Ccl5; Tmsb10 | Ifi27l2a; Ccr7; Ly6d; Rgcc | ||||
| K19 | Prl8a9; Tpbpa; Psg21; Prl3b1; Creg1 | Cts6; Ccr10 | ||||
| K20 | CD8.K | LCMVarm_intravascular | Cenpa; Ube2c; Cdc20; Cenpf; Arl6ip1 | H2ac8; H1f5; H1f4; Hist1h2ap; H1f3 |
Table S1. One row per GP: which Level-1 (major lineage), Level-2 (sub-lineage), condition, and organ categories it predicts well (AUC > 0.8, driven by high loading), plus its top 5 positive and negative signature genes (|score| > 0.25).
sessionInfo()R version 4.5.1 (2025-06-13)
Platform: aarch64-apple-darwin20
Running under: macOS Sequoia 15.6.1
Matrix products: default
BLAS: /System/Library/Frameworks/Accelerate.framework/Versions/A/Frameworks/vecLib.framework/Versions/A/libBLAS.dylib
LAPACK: /Library/Frameworks/R.framework/Versions/4.5-arm64/Resources/lib/libRlapack.dylib; LAPACK version 3.12.1
locale:
[1] en_CA/en_CA/en_CA/C/en_CA/en_CA
time zone: Asia/Tokyo
tzcode source: internal
attached base packages:
[1] stats graphics grDevices utils datasets methods base
loaded via a namespace (and not attached):
[1] vctrs_0.7.3 cli_3.6.6 knitr_1.50 rlang_1.2.0
[5] xfun_0.55 stringi_1.8.7 otel_0.2.0 promises_1.5.0
[9] jsonlite_2.0.0 workflowr_1.7.2 glue_1.8.1 rprojroot_2.1.1
[13] git2r_0.36.2 htmltools_0.5.9 httpuv_1.6.16 sass_0.4.10
[17] rmarkdown_2.30 evaluate_1.0.5 jquerylib_0.1.4 tibble_3.3.0
[21] fastmap_1.2.0 yaml_2.3.12 lifecycle_1.0.5 whisker_0.4.1
[25] stringr_1.6.0 compiler_4.5.1 fs_1.6.6 Rcpp_1.1.1-1.1
[29] pkgconfig_2.0.3 later_1.4.4 digest_0.6.39 R6_2.6.1
[33] pillar_1.11.1 magrittr_2.0.5 bslib_0.9.0 tools_4.5.1
[37] cachem_1.1.0