CytoProfile
The goal of CytoProfile is to conduct quality control using biological meaningful cutoff on raw measured values of cytokines. Specifically, test on distributional symmetry to suggest the adopt of transformation. Conduct exploratory analysis including summary statistics, generate enriched barplots, and boxplots. Further, conduct univariate analysis and multivariate analysis for advance analysis.
Installation
Before installation of the CytoProfile package, make sure to install BiocManager and mixOmics packages using:
## install BiocManager
if (!requireNamespace("BiocManager", quietly = TRUE)) install.packages("BiocManager")
## install mixOmics
BiocManager::install('mixOmics')You can install the development version of CytoProfile from GitHub with:
Install CytoProfile from CRAN with:
Example
Below are examples of using the functions provided in CytoProfile. Any saved or generated files that are PDF or PNG format will be found at in the Figures Folder.
1. Data Loading and set up
# Loading all packages required
# Data manipulation and reshaping
library(dplyr) # For data filtering, grouping, and summarising.
library(tidyr) # For reshaping data (e.g., pivot_longer, pivot_wider).
# Plotting and visualization
library(ggplot2) # For creating all the ggplot-based visualizations.
library(gridExtra) # For arranging multiple plots on a single page.
library(ggrepel) # For improved label placement in plots (e.g., volcano plots).
library(gplots) # For heatmap.2, which is used to generate heatmaps.
library(plot3D) # For creating 3D scatter plots in PCA and sPLS-DA analyses.
library(reshape2) # For data transformation (e.g., melt) in cross-validation plots.
# Statistical analysis
library(mixOmics) # For multivariate analyses (PCA, sPLS-DA, etc.).
library(e1071) # For computing skewness and kurtosis.
library(pROC) # For ROC curve generation in machine learning model evaluation.
# Machine learning
library(xgboost) # For building XGBoost classification models.
library(randomForest) # For building Random Forest classification models.
library(caret) # For cross-validation and other machine learning utilities.
# Package development and document rendering
library(knitr) # For knitting RMarkdown files and setting chunk options.
library(devtools) # For installing the development version of the package from GitHub.
# Load in the CytoProfile package
library(CytoProfile)
# Loading in data
data("ExampleData1")
data_df <- ExampleData12. Exploratory Data Analysis
Boxplots
# Generating boxplots to check for outliers for raw values
cyt_bp(data_df[, -c(1:3)], pdf_title = NULL)
# Removing the first 3 columns to retain only continuous variables.
# Generating boxplots to check for outliers for log2 values
cyt_bp(data_df[, -c(1:3)], pdf_title = NULL, scale = "log2")
3. Skewness and Kurtosis
data_df <- ExampleData1
# Histogram for overall raw data
cyt_skku(data_df[, -c(1:3)], pdf_title = NULL, group_cols = NULL)
# Histogram with grouping (e.g., "Group")
cyt_skku(ExampleData1[, -c(2:3)], pdf_title = NULL, group_cols = c("Group"))
4. Error Bar Plots
Basic Error Bar Plot
# Generating basic error bar plots
data_df <- ExampleData1
cyt_errbp(
data_df[, c("Group", "CCL.20.MIP.3A", "IL.10")],
group_col = "Group",
p_lab = FALSE,
es_lab = FALSE,
class_symbol = FALSE,
x_lab = "Cytokines",
y_lab = "Concentrations in log2 scale",
log2 = TRUE
)
Enriched Error Bar Plot with p-values and Effect Sizes
# Generating Error Bar Plot enriched with p-value and effect size
data_df <- ExampleData1
cyt_errbp(
data_df[, c("Group", "CCL.20.MIP.3A", "IL.10")],
group_col = "Group",
p_lab = TRUE,
es_lab = TRUE,
class_symbol = TRUE,
x_lab = "Cytokines",
y_lab = "Concentrations in log2 scale",
log2 = TRUE
)
5. Univariate Analysis
Two Sample T-test and Mann Whitney U Test
# Performing Test
data_df <- ExampleData1[, -c(3)]
data_df <- dplyr::filter(data_df, Group != "ND", Treatment != "Unstimulated")
# Test example
cyt_ttest(
data_df[, c(1:2, 5:6)],
scale = "log2",
verbose = TRUE,
format_output = TRUE
)
#> $results
#> Outcome Categorical Comparison
#> 1 IFN.G Group PreT2D vs T2D
#> 2 IL.10 Group PreT2D vs T2D
#> 3 IFN.G Treatment CD3/CD28 vs LPS
#> 4 IL.10 Treatment CD3/CD28 vs LPS
#> Test Estimate Statistic P_value
#> 1 Wilcoxon rank sum test with continuity correction -2.463 1599.0 0.008
#> 2 Wilcoxon rank sum test with continuity correction -0.956 1625.0 0.012
#> 3 Wilcoxon rank sum test with continuity correction 9.024 4132.5 0.000
#> 4 Wilcoxon rank sum test with continuity correction 1.690 3091.0 0.000ANOVA Comparisons Test
# Perform ANOVA comparisons test (example with 2 cytokines)
data_df <- ExampleData1[, -c(3)]
cyt_anova(data_df[, c(1:2, 5:6)], format_output = TRUE)
#> Outcome Categorical Comparison P_adj
#> PreT2D-ND IFN.G Group PreT2D-ND 0.0883
#> T2D-ND IFN.G Group T2D-ND 0.9779
#> T2D-PreT2D IFN.G Group T2D-PreT2D 0.0550
#> PreT2D-ND1 IL.10 Group PreT2D-ND 0.7745
#> T2D-ND1 IL.10 Group T2D-ND 0.1546
#> T2D-PreT2D1 IL.10 Group T2D-PreT2D 0.0316
#> LPS-CD3/CD28 IFN.G Treatment LPS-CD3/CD28 0.0000
#> Unstimulated-CD3/CD28 IFN.G Treatment Unstimulated-CD3/CD28 0.0000
#> Unstimulated-LPS IFN.G Treatment Unstimulated-LPS 0.9988
#> LPS-CD3/CD281 IL.10 Treatment LPS-CD3/CD28 0.0000
#> Unstimulated-CD3/CD281 IL.10 Treatment Unstimulated-CD3/CD28 0.0000
#> Unstimulated-LPS1 IL.10 Treatment Unstimulated-LPS 0.00016. Multivariate Analysis
Partial Least Squares Discriminant Analysis (PLS-DA)
# cyt_plsda function.
data <- ExampleData1[, -c(3)]
data_df <- dplyr::filter(data, Group != "ND" & Treatment == "CD3/CD28")
cyt_splsda(
data_df,
pdf_title = NULL,
colors = c("black", "purple"),
bg = FALSE,
scale = "log2",
ellipse = TRUE,
conf_mat = FALSE,
var_num = 25,
cv_opt = "loocv",
comp_num = 2,
pch_values = c(16, 4),
group_col = "Group",
group_col2 = "Treatment",
roc = TRUE
)
7. Principal Component Analysis (PCA)
data <- ExampleData1[, -c(3, 23)]
data_df <- dplyr::filter(data, Group != "ND" & Treatment != "Unstimulated")
cyt_pca(
data_df,
pdf_title = NULL,
colors = c("black", "red2"),
scale = "log2",
comp_num = 2,
pch_values = c(16, 4),
group_col = "Group"
)
#> [1] "Results based on log2 transformation:"
8. Volcano Plot
# Generating Volcano Plot
data_df <- ExampleData1[, -c(2:3)]
cyt_volc(
data_df,
group_col = "Group",
cond1 = "T2D",
cond2 = "ND",
fold_change_thresh = 2.0,
top_labels = 15
)
#> $`T2D vs ND`
9. Heatmap
# Generating Heat map
cyt_heatmap(
data = data_df,
scale = "log2", # Optional scaling
annotation_col_name = "Group",
title = NULL
)
10. Dual Flashlight Plot
# Generating dual flashlights plot
data_df <- ExampleData1[, -c(2:3)]
dfp <- cyt_dualflashplot(
data_df,
group_var = "Group",
group1 = "T2D",
group2 = "ND",
ssmd_thresh = -0.2,
log2fc_thresh = 1,
top_labels = 10
)
# Print the plot
dfp
# Print the table data used for plotting
print(dfp$data, n = 25)
#> # A tibble: 25 × 11
#> cytokine mean_ND mean_PreT2D mean_T2D variance_ND variance_PreT2D
#> <chr> <dbl> <dbl> <dbl> <dbl> <dbl>
#> 1 CCL.20.MIP.3A 634. 404. 887. 6.72e+ 5 2.74e+5
#> 2 GM.CSF 2.65 3.11 1.92 2.63e+ 1 3.14e+1
#> 3 IFN.G 57730. 18303. 61484. 2.86e+10 2.30e+9
#> 4 IL.10 979. 836. 1366. 1.99e+ 6 1.19e+6
#> 5 IL.12.P70 13.0 39.1 78.9 4.15e+ 2 2.56e+4
#> 6 IL.13 1064. 1543. 1122. 5.60e+ 6 1.11e+7
#> 7 IL.15 7.92 4.29 8.22 3.54e+ 1 2.58e+1
#> 8 IL.17A 352. 653. 615. 9.40e+ 5 2.88e+6
#> 9 IL.17E.IL.25 0.0101 0.0163 0.01 1.01e- 6 3.88e-3
#> 10 IL.17F 1.63 2.35 3.11 1.56e+ 1 3.37e+1
#> 11 IL.1B 2806. 2977. 4299. 6.63e+ 7 3.76e+7
#> 12 IL.2 9227. 10718. 16129. 2.60e+ 8 4.10e+8
#> 13 IL.21 205. 210. 316. 3.15e+ 5 2.49e+5
#> 14 IL.22 0.0513 0.0684 0.0633 4.58e- 3 4.51e-3
#> 15 IL.23 0.147 0.243 0.269 3.13e- 2 9.37e-2
#> 16 IL.27 0.0662 0.0834 0.106 6.18e- 3 5.66e-3
#> 17 IL.28A 0.0537 0.0710 0.0666 2.45e- 3 5.10e-3
#> 18 IL.31 0.0409 0.0905 0.0354 6.62e- 3 4.88e-2
#> 19 IL.33 1.17 1.43 1.16 2.09e+ 0 2.71e+0
#> 20 IL.4 0.344 0.707 0.297 4.24e- 1 2.96e+0
#> 21 IL.5 134. 340. 155. 1.09e+ 5 9.88e+5
#> 22 IL.6 4620. 5197. 8925. 2.86e+ 7 5.72e+7
#> 23 IL.9 203. 256. 254. 1.34e+ 5 2.11e+5
#> 24 TNF.A 5046. 3069. 5624. 7.02e+ 7 1.63e+7
#> 25 TNF.B 0.641 0.709 0.610 2.37e+ 0 2.76e+0
#> # ℹ 5 more variables: variance_T2D <dbl>, ssmd <dbl>, log2FC <dbl>,
#> # SSMD_Category <chr>, Significant <lgl>
11. Machine Learning Models
Using XGBoost for classification
# Using XGBoost for classification
data_df0 <- ExampleData1
data_df <- data.frame(data_df0[, 1:3], log2(data_df0[, -c(1:3)]))
data_df <- data_df[, -c(2:3)]
data_df <- dplyr::filter(data_df, Group != "ND")
cyt_xgb(
data = data_df,
group_col = "Group",
nrounds = 500,
max_depth = 4,
eta = 0.05,
nfold = 5,
cv = TRUE,
eval_metric = "mlogloss",
early_stopping_rounds = NULL,
top_n_features = 10,
verbose = 0,
plot_roc = TRUE,
print_results = FALSE
)
