CyteTypeR Annotation using AI_seurat_clusters

1 load libraries

2 Load Seurat Object

2.1 Dimplot by cell_state

DimPlot(All_samples_Merged, group.by = "seurat_clusters", label = F, label.box = T,repel = T, reduction = "umap")

3 Run CyteTypeR for cluster annotation

Idents(All_samples_Merged) <- "seurat_clusters"

# ---------------------------------------------------------
# Find marker genes per cluster
# ---------------------------------------------------------
SS_markers <- FindAllMarkers(
  All_samples_Merged,
  only.pos = TRUE,
  min.pct = 0.25,
  logfc.threshold = 0.25,
  min.pct.diff = 0.2
  
)

library(dplyr)

# Precise blacklist for uninformative genes
blacklist_patterns <- c(
  "^TRAV", "^TRBV", "^TRGV", "^TRDV", "^TRBC", "^TRAC", "^TRDC", "^TRGC", # TCR
  "^IGH", "^IGK", "^IGL", "^IGJ",                                         # Ig genes
  "^RPL", "^RPS",                                                         # ribosomal
  "^MT-",                                                                 # mitochondria
  "^HBA", "^HBB", "^HB[ABZ]",                                             # hemoglobins
  "^NEAT1$", "^MALAT1$",                                                  # optional lncRNAs
  "^XIST$"                              )

blacklist_regex <- paste(blacklist_patterns, collapse = "|")

# Preview which markers will be removed
to_remove <- SS_markers %>%
  filter(grepl(blacklist_regex, gene, ignore.case = TRUE))
message("Rows to remove: ", nrow(to_remove))
head(to_remove$gene)

# Filter markers (keep important metabolic/proliferation genes)
SS_markers_filtered <- SS_markers %>%
  filter(!grepl(blacklist_regex, gene, ignore.case = TRUE))

# Extract top 100 markers per cluster
top100_markers <- SS_markers_filtered %>%
  filter(p_val_adj < 0.05) %>%  # ensure statistical significance
  group_by(cluster) %>%
  slice_max(order_by = avg_log2FC, n = 100) %>%
  ungroup()

# Save to CSV
write.csv(SS_markers_filtered, 
          file = "seurat_cluster_filtered_all_markers.csv",
          row.names = FALSE)

# Save to CSV
write.csv(top100_markers, 
          file = "Top100_markers_per_seurat_cluster_filtered.csv",
          row.names = FALSE)

4 Run CyteTypeR for cluster annotation

library(CyteTypeR)
library(dplyr)
# -------------------------------
# Prepare data for CyteTypeR
# -------------------------------
prepped_data <- PrepareCyteTypeR(
  All_samples_Merged,
  SS_markers_filtered,
  n_top_genes = 25,               # top 100 marker genes per cluster
  group_key = 'seurat_clusters',  
  aggregate_metadata = TRUE,
  coordinates_key = "umap"
)

INFO [2026-02-04 15:53:58] Checking markers table...
INFO [2026-02-04 15:53:58] Provided markers data is a dataframe ✔
INFO [2026-02-04 15:53:58] No NA values ✔
INFO [2026-02-04 15:53:58] 'cluster' column found in marker table ✔
INFO [2026-02-04 15:53:58] Found gene symbols ✔
INFO [2026-02-04 15:53:58] Correct cluster labels ✔
INFO [2026-02-04 15:53:58] Markers check: done ✔

[1] "Aggregating metadata..."
[1] "Preparing marker genes with top 25 genes..."
[1] "Preparing visualisation data..."
[1] "Calculating expression percentages..."

INFO [2026-02-04 15:54:02] Processed batch 1/19 (2000 genes)
INFO [2026-02-04 15:54:07] Processed batch 2/19 (2000 genes)
INFO [2026-02-04 15:54:12] Processed batch 3/19 (2000 genes)
INFO [2026-02-04 15:54:19] Processed batch 4/19 (2000 genes)
INFO [2026-02-04 15:54:26] Processed batch 5/19 (2000 genes)
INFO [2026-02-04 15:54:35] Processed batch 6/19 (2000 genes)
INFO [2026-02-04 15:54:44] Processed batch 7/19 (2000 genes)
INFO [2026-02-04 15:54:55] Processed batch 8/19 (2000 genes)
INFO [2026-02-04 15:55:07] Processed batch 9/19 (2000 genes)
INFO [2026-02-04 15:55:20] Processed batch 10/19 (2000 genes)
INFO [2026-02-04 15:55:34] Processed batch 11/19 (2000 genes)
INFO [2026-02-04 15:55:50] Processed batch 12/19 (2000 genes)
INFO [2026-02-04 15:56:06] Processed batch 13/19 (2000 genes)
INFO [2026-02-04 15:56:24] Processed batch 14/19 (2000 genes)
INFO [2026-02-04 15:56:43] Processed batch 15/19 (2000 genes)
INFO [2026-02-04 15:57:04] Processed batch 16/19 (2000 genes)
INFO [2026-02-04 15:57:25] Processed batch 17/19 (2000 genes)
INFO [2026-02-04 15:57:48] Processed batch 18/19 (2000 genes)
INFO [2026-02-04 15:57:56] Processed batch 19/19 (601 genes)
INFO [2026-02-04 15:57:56] Processed 19 batches and a total of 36601 genes

[1] "Done!"

# -------------------------------
# Metadata for CyteTypeR
# -------------------------------
metadata <- list(
  title = 'My scRNA-seq analysis of human Sézary syndrome ',
  run_label = 'initial_analysis',
  experiment_name = 'Sézary Syndrome Cell_lines human samples study'
)


# Remove both literal "NA" and true NA names
prepped_data$clusterMetadata <- prepped_data$clusterMetadata[
  !is.na(names(prepped_data$clusterMetadata)) & 
  names(prepped_data$clusterMetadata) != "NA"
]

# Confirm cleanup
names(prepped_data$clusterMetadata)

 [1] "1"  "2"  "3"  "4"  "5"  "6"  "7"  "8"  "9"  "10" "11" "12" "13" "14"

# -------------------------------
# Run CyteTypeR
# -------------------------------
results <- CyteTypeR(
  obj = All_samples_Merged,
  prepped_data = prepped_data,
  study_context = "Sezary syndrome Cell lines L1-L7 in orig.ident derived from blood samples from humans and CD4T_lab and CD4T_10x which are cluster 3 and 10 are purified samples from healthy donors patient samples",
  metadata = metadata
)

INFO [2026-02-04 15:58:38] Submitting job to CyteType...
INFO [2026-02-04 16:00:15] CyteType job (id: 5a2cb8c4-db28-428e-81b9-617c046e2ce4) submitted. Polling for results...
INFO [2026-02-04 16:00:20] Report (updates automatically) available at: 
INFO [2026-02-04 16:00:20] If disconnected, retrieve results with: GetResults()

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WARN [2026-02-04 16:15:40] Job 5a2cb8c4-db28-428e-81b9-617c046e2ce4 has unknown status: 'error'. Continuing...

[DONE] [✔✔✔✔✔✔✔✔✔✔✔✔✔✔] 14/14 completed

INFO [2026-02-04 16:16:36] Job 5a2cb8c4-db28-428e-81b9-617c046e2ce4 completed successfully.

# -------------------------------
# Check results
# -------------------------------
# If job succeeds, retrieve results:
# GetResults(results)

saveRDS(results, file = "CyteTypeR_results_SS_cclusters_finalized.rds")

5 Run CyteTypeR for cluster Visualization

DimPlot(results, group.by = "cytetype_seurat_clusters", label = T, label.box = T,repel = T, reduction = "umap")
DimPlot(results, group.by = "cytetype_seurat_clusters", label = F, label.box = T,repel = T, reduction = "umap")

6 https://nygen-labs-prod--cytetype-api.modal.run/report/5a2cb8c4-db28-428e-81b9-617c046e2ce4