--- title: "Pk/Pv/Pf Serology Tutorial" output: rmarkdown::html_vignette vignette: > %\VignetteIndexEntry{Pk/Pv/Pf Serology Tutorial} %\VignetteEngine{knitr::rmarkdown} %\VignetteEncoding{UTF-8} --- ```{r, include = FALSE} knitr::opts_chunk$set( collapse = TRUE, comment = "#>" ) options(rmarkdown.html_vignette.check_title = FALSE) setup <- function() { needed <- c("knitr", "rmarkdown", "tidyverse", "kableExtra") lapply(needed, function(pkg) { if (requireNamespace(pkg, quietly = TRUE)) { library(pkg, character.only = TRUE) } }) } setup() library(SeroTrackR) ``` For all of these analyses you can run as many plates as you wish. ### Visualisation of the Pk/Pv/Pf Pipeline ![](../man/figures/SeroTrackR_Pk_Pf_Pv.jpeg) ```{r setup pk analysis, eval=FALSE} library(SeroTrackR) library(tidyverse) ``` ### 5-Point Standard Curve #### Step 1: Load your data! Firstly, we will be using our example data that's in-built in the package. Here replace the `system.file()` argument with the file path for your package. ```{r} your_raw_data_5std <- c( system.file("extdata", "example_MAGPIX_pk_5std_plate1.csv", package = "SeroTrackR"), system.file("extdata", "example_MAGPIX_pk_5std_plate2.csv", package = "SeroTrackR") ) your_plate_layout_5std <- system.file("extdata", "example_platelayout_pk_5std.xlsx", package = "SeroTrackR") ``` #### Step 2: Read your data and process MFI to RAU This function to (a) process raw Serological data and (b) convert MFI to RAU. The `runPlasmoPipeline()` function will output three data frames: 1. All_Results: All columns of every MFI to RAU conversion 2. MFI_RAU: Just the SampleID, Plate, MFI and RAU values per antigen 3. MFI_RAU_long: SampleID, Plate, MFI, RAU, Antigen, Species (long-format df) ```{r} results_5stdcurve <- runPlasmoPipeline( raw_data = your_raw_data_5std, platform = "magpix", plate_layout = your_plate_layout_5std, panel = "panel1", std_point = 5, experiment_name = "5-point standard curve" ) ``` ##### Standard Curve Plot ```{r} results_5stdcurve$std_curve ``` ##### Bead Counts QC Plot ```{r} results_5stdcurve$bead_counts ``` ##### Blanks QC Ploat ```{r} results_5stdcurve$blanks ``` ##### MFI to RAU Tables All results: ```{r} results_5stdcurve$mfi_outputs$All_Results %>% head() %>% kable() ``` MFI and RAU only: ```{r} results_5stdcurve$mfi_outputs$MFI_RAU %>% head() %>% kable() ``` MFI and RAU long table: ```{r} results_5stdcurve$mfi_outputs$MFI_RAU_long %>% head() %>% kable() ``` ### 10-Point Standard Curve These steps are very similar to the 5-point standard curve, except where indicated. #### Step 1: Load your data! ```{r} your_raw_data_10std <- c( system.file("extdata", "example_MAGPIX_pk_10std_plate1.csv", package = "SeroTrackR"), system.file("extdata", "example_MAGPIX_pk_10std_plate2.csv", package = "SeroTrackR") ) your_plate_layout_10std <- system.file("extdata", "example_platelayout_pk_10std.xlsx", package = "SeroTrackR") ``` #### Step 2: Read your data and process MFI to RAU ```{r} results_10stdcurve <- runPlasmoPipeline( raw_data = your_raw_data_10std, platform = "magpix", plate_layout = your_plate_layout_10std, panel = "panel1", std_point = 10, ################################### here make sure you write 10! experiment_name = "10-point standard curve" ) ``` ##### Standard Curve Plot ```{r} results_10stdcurve$std_curve ``` ##### Bead Counts QC Plot ```{r} results_10stdcurve$bead_counts ``` ##### Blanks QC Ploat ```{r} results_10stdcurve$blanks ``` ##### MFI to RAU Tables All results: ```{r} results_10stdcurve$mfi_outputs$All_Results %>% head() %>% kable() ``` MFI and RAU only: ```{r} results_10stdcurve$mfi_outputs$MFI_RAU %>% head() %>% kable() ``` MFI and RAU long table: ```{r} results_10stdcurve$mfi_outputs$MFI_RAU_long %>% head() %>% kable() ```