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library(SingleCellExperiment)
library(dplyr)
library(ggplot2)
library(tibble)
library(purrr)
library(forcats)
library(topconfects)
library(patchwork)
library(tidyr)

source(here::here("code", "analysis-utils.R"))
source(here::here("code", "plot-utils.R"))
real_data_data <- retrieve_real_data_parameters() %>% 
  rowwise() %>% 
  mutate(mgs = list(readRDS(full_filename)$result)) %>%
  ungroup()

pbmc3k <- readRDS(here::here("data", "real_data", "zeisel.rds"))
real_data_data %>% 
  filter(data_id == "endothelial") %>% 
  filter(method != "rankcorr", method != "difference", method != "lm", 
         pars != "seurat_roc", method != "random") %>% 
  rowwise() %>% 
  mutate(n_zero = nrow(filter(mgs, p_value == 0))) %>% 
  ungroup() %>% 
  mutate(pars_plot = pars_lookup[pars]) %>% 
  mutate(pars_plot = fct_reorder(factor(pars_plot), n_zero)) %>% 
  ggplot(aes(pars_plot, n_zero)) + 
  geom_col(fill = "seagreen") + 
  coord_flip() +
  labs(y = "Number of 0 p-values", 
       x = "Method", 
       title = "Number of 0 p-values - Endothelial data") + 
  theme_bw()

real_data_data %>% 
  filter(data_id == "zeisel") %>% 
  filter(method != "rankcorr", method != "difference", method != "lm", 
         pars != "seurat_roc", method != "random", pars != "seurat_poisson") %>% 
  rowwise() %>% 
  mutate(n_zero = nrow(filter(mgs, p_value == 0))) %>% 
  ungroup() %>% 
  mutate(pars_plot = pars_lookup[pars]) %>% 
  mutate(pars_plot = fct_reorder(factor(pars_plot), n_zero)) %>% 
  ggplot(aes(pars_plot, n_zero)) + 
  geom_col(fill = "seagreen") + 
  coord_flip() +
  labs(y = "Number of 0 p-values", 
       x = "Method", 
       title = "Number of 0 p-values - Zeisel data") + 
  theme_bw()

real_data_data %>% 
  filter(data_id == "pbmc3k") %>% 
  filter(method != "rankcorr", method != "difference", method != "lm", 
         pars != "seurat_roc", method != "random", pars != "seurat_poisson") %>% 
  rowwise() %>% 
  mutate(n_zero = nrow(filter(mgs, p_value == 0))) %>% 
  ungroup() %>% 
  mutate(pars_plot = pars_lookup[pars]) %>% 
  mutate(pars_plot = fct_reorder(factor(pars_plot), n_zero)) %>% 
  ggplot(aes(pars_plot, n_zero)) + 
  geom_col(fill = "seagreen") + 
  coord_flip() +
  labs(y = "Number of 0 p-values", 
       x = "Method", 
       title = "Number of 0 p-values - pbmc3k data") + 
  theme_bw()

seurat_wilcox_zeisel <- readRDS(
  here::here("results", "real_data", "zeisel-seurat_wilcox.rds")
)

scanpy_wilcoxon_tc_zeisel <- readRDS(
  here::here("results", "real_data", "zeisel-scanpy_wilcoxontiecorrect_rankby_raw.rds")
)
scanpy_genes <- scanpy_wilcoxon_tc_zeisel %>% 
  pluck("result") %>% 
  filter(cluster == "oligodendrocytes") %>% 
  get_top_sel_mgs(n = 40) %>% 
  pull("gene")
  
seurat_genes <- seurat_wilcox_zeisel %>% 
  pluck("result") %>% 
  filter(cluster == "oligodendrocytes") %>% 
  get_top_sel_mgs(n = 40) %>% 
  pull("gene")

rank_rank_plot(
  scanpy_genes,
  seurat_genes,
  "Scanpy Wilcoxon TC (rankby_abs)", 
  "Seurat Wilcox"
) + 
  ggtitle("Scanpy vs Seurat Wilcoxon (zero p-values)")

all_datasets_results <- retrieve_real_data_parameters() %>% 
  rowwise() %>% 
  mutate(
    mgs_raw = list(readRDS(full_filename)$result), 
    mgs = list(split(mgs_raw, mgs_raw$cluster))
  ) %>% 
  ungroup() %>% 
  unnest_longer(
    col = mgs, 
    values_to = "mgs", 
    indices_to = "cluster"
  )
scanpy_seurat_zeisel_oligodendrocytes <- all_datasets_results %>%
  mutate(n = 125) %>% 
  filter(data_id == "zeisel") %>% 
  filter(
    pars %in% c("scanpy_wilcoxontiecorrect_rankby_abs", "seurat_wilcox")
  ) %>% 
  filter(cluster == "oligodendrocytes") %>%
  rowwise() %>% 
  mutate(mgs = list(get_top_sel_mgs(mgs, n = n))) %>% 
  mutate(
    rank = list(1:n), 
    log_fc = list(mgs$log_fc), 
    p_value = list(mgs$p_value),
    zero_p_value = list(p_value == 0)
  ) %>% 
  mutate(plot_method = method_lookup[method]) %>% 
  unnest(cols = c(rank, log_fc, zero_p_value)) %>% 
  # Shrink plot file size.
  select(-c(mgs, mgs_raw)) %>% 
  ggplot(aes(x = rank, y = log_fc, colour = zero_p_value)) + 
  geom_point() + 
  facet_wrap(~plot_method) + 
  labs(
    x = "Gene rank", 
    y = "Log fold-change", 
    colour = "p-value = 0?", 
  ) + 
  scale_colour_manual(values = c("black", "red")) + 
  theme_bw()

scanpy_seurat_zeisel_oligodendrocytes

saveRDS(
  scanpy_seurat_zeisel_oligodendrocytes,
  here::here("figures", "raw", "scanpy-seurat-zeisel-oligodendrocytes.rds")
)

devtools::session_info()
─ Session info  ──────────────────────────────────────────────────────────────
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 date     2024-01-01
 pandoc   2.18 @ /apps/easybuild-2022/easybuild/software/MPI/GCC/11.3.0/OpenMPI/4.1.4/RStudio-Server/2022.07.2+576-Java-11-R-4.1.2/bin/pandoc/ (via rmarkdown)

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