Cell type labelling

Will Macnair - Computational Sciences Center of Excellence, F Hoffmann-La Roche Ltd, Basel, Switzerland

March 23, 2026

Integration clusters vs predicted cell types

Prediction of cell type labels is a two-step process: The labeller first assigns a predicted cell type to each individual cell. These cell-level predictions are then aggregated at the level of high-resolution clusters (a majority-voting approach is used, where the final, assigned label for a cluster is the most common predicted label among all the cells within it).

The heatmap helps to assess whether this aggregation step seems sensible. Each cell on the heatmap shows the proportion of cells within a cluster (on the x-axis) that are assigned a specific predicted cell type in the first step (on the y-axis).

for (ii in seq_along(guess_f_ls)) {
  # unpack
  this_labeller   = labeller_ls[[ ii ]]
  this_model      = model_ls[[ ii ]]
  this_hi_res_cl  = hi_res_cl_ls[[ ii ]]

  # make confusion matrix
  guesses_sel = guesses_ls[[ ii ]] %>% 
    .[, .(cell_id, prediction = predicted_label_naive %>% factor)]
  int_tmp     = int_dt[, .(cell_id, UMAP1, UMAP2, hi_res_cl = get(this_hi_res_cl) %>% fct_infreq)]
  confuse_dt  = calc_confuse_dt(guesses_sel, int_tmp, "prediction", "hi_res_cl", min_cl2_p = min_cl2_p)

  # plot heatmap
  cat('### ', this_labeller, ', ', this_model, '\n', sep = '')
  draw(plot_cluster_comparison_heatmap(confuse_dt, "prediction", this_hi_res_cl, 
    plot_var = 'log_p_cl2', do_sort = "hclust"), merge_legend = TRUE)
  cat('\n\n')
}

scprocess, human_cns

Predicted cell types over UMAP

Clustering of data is performed with different labellers and models. Each of these is shown over a UMAP together with a plot showing predicted cell type labels.

for (ii in seq_along(guess_f_ls)) {
  # unpack
  this_labeller   = labeller_ls[[ ii ]]
  this_model      = model_ls[[ ii ]]
  this_hi_res_cl  = hi_res_cl_ls[[ ii ]]

  # get data
  guesses_sel = guesses_ls[[ ii ]] %>% 
    .[, .(cell_id, prediction = predicted_label_agg %>% factor)]
  int_tmp     = int_dt[, .(cell_id, UMAP1, UMAP2, hi_res_cl = get(this_hi_res_cl) %>% fct_infreq)]

  # plots
  g_cl        = plot_umap_cluster(int_dt, 
    int_tmp[, .(cell_id, cluster = hi_res_cl)], "high resolution\nharmony\ncluster")
  g_pred      = plot_umap_cluster(int_dt, 
    guesses_sel[, .(cell_id, cluster = prediction)], "prediction\n(aggregated)")
  g = g_cl + g_pred

  # plot umaps
  cat('### ', this_labeller, ', ', this_model, '\n', sep = '')
  print(g)
  cat('\n\n')
}

scprocess, human_cns

Totals for each predicted cell type

Tables showing how many in total of each celltype are predicted for each label, for each combination of labeller and model.

for (ii in seq_along(guess_f_ls)) {
  # unpack
  this_labeller   = labeller_ls[[ ii ]]
  this_model      = model_ls[[ ii ]]

  # print table
  cat('### ', this_labeller, ', ', this_model, '\n', sep = '')
  guesses_ls[[ ii ]] %>% calc_labels_table %>% kbl("html") %>% row_spec(row = 0, bold = TRUE) %>%
    kable_styling(bootstrap_options = "striped", full_width = FALSE, font_size = 12, position = "center") %>%
    scroll_box(width = "60%", height = "500px") %>% print
  cat('\n\n')
}

scprocess, human_cns

predicted label no. cells, aggregated no. cells, not aggregated
Neurons 72214 68311
Oligodendrocyte 8566 8579
Micro_Mono 6407 6307
Vascular_Fibro 5017 5491
Astrocyte 2150 2232
OPC_COP 456 3200
T_NK_B_cell 0 562
Ependymal_ChorPlex 0 128

R session info

Details of the R package versions used are given below.

devtools::session_info()
## ─ Session info ───────────────────────────────────────────────────────────────
##  setting  value
##  version  R version 4.4.3 (2025-02-28)
##  os       Red Hat Enterprise Linux 8.10 (Ootpa)
##  system   x86_64, linux-gnu
##  ui       X11
##  language (EN)
##  collate  en_US.UTF-8
##  ctype    en_US.UTF-8
##  tz       Europe/Zurich
##  date     2026-03-25
##  pandoc   3.8.2.1 @ /home/macnairw/packages/scprocess/.snakemake/conda/4fef11cadd34f9d2d13a0d6139d09340_/bin/ (via rmarkdown)
##  quarto   NA
## 
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##  whisker                0.4.1    2022-12-05 [1] CRAN (R 4.4.3)
##  withr                  3.0.2    2024-10-28 [1] CRAN (R 4.4.3)
##  workflowr            * 1.7.2    2025-08-18 [1] CRAN (R 4.4.3)
##  xfun                   0.54     2025-10-30 [1] CRAN (R 4.4.3)
##  xgboost              * 3.1.2.1  2026-01-06 [1] local
##  xml2                   1.5.0    2025-11-17 [1] CRAN (R 4.4.3)
##  xtable                 1.8-4    2019-04-21 [1] CRAN (R 4.4.3)
##  XVector                0.46.0   2024-10-29 [1] Bioconductor 3.20 (R 4.4.2)
##  yaml                 * 2.3.11   2025-11-28 [1] CRAN (R 4.4.3)
##  zellkonverter        * 1.16.0   2024-10-29 [1] Bioconductor 3.20 (R 4.4.2)
##  zlibbioc               1.52.0   2024-10-29 [1] Bioconductor 3.20 (R 4.4.2)
##  zoo                    1.8-14   2025-04-10 [1] CRAN (R 4.4.3)
## 
##  [1] /home/macnairw/packages/scprocess/.snakemake/conda/4fef11cadd34f9d2d13a0d6139d09340_/lib/R/library
##  * ── Packages attached to the search path.
## 
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