knitr::opts_chunk$set(
    collapse = TRUE,
    comment = "#>"
)

Introduction

GladiaTOX is an open-source solution for HCS data processing and reporting that expands the tcpl package (toxcast pipeline, Filer et al., 2016). In addition to tcpl's functionalities (multiple dose-response fitting and best fit selection), GladiaTOX

Installation and package load

if(!requireNamespace("BiocManager", quietly = TRUE))
    install.packages("BiocManager")
BiocManager::install("GladiaTOX")
# Load GladiaTOX package and setup an output directory
# Change outdir accordingly to the folder path you want the reports to be saved
library(GladiaTOX)
outdir <- getwd()
wzxhzdk:3

Database configuration

The GladiaTOX installation includes the deployment of a sqlite database (sql/gladiatoxdb.sqlite folder). This file contains the database structure already initialized with the necessary content needed for data processing (e.g. processing methods entries).

The first step after database deployment is to configure access parameters. The default configuration already points to the sqlite database at so no additional configurations are needed to complete the example below. Below the default database URL is assigned to the variable sqlite_src:

sqlite_src <- file.path(system.file(package="GladiaTOX"), "sql",
                        "gladiatoxdb.sqlite")

The gtoxConf configuration command below initializes all necessary variables.

# sqlite database location
gtoxConf(   drvr = "SQLite",
            host = NA,
            user = NA,
            pass = NULL,
            db = sqlite_src)

This database will be used in next sections to load and process a second study phase. The sqlite database can be seen as a sample database used for the following example.

In case users plan to use the package in production and for multiple studies, it is recommended to install the MariaDB database (sql/gladiatoxdb_structure.mysql). This file contains SQL instructions to create and initialize an MariaDB database.

In case you install the database schema or change location of the sqlite database, then you must run the configuration command below and point to the new database location. For example, in case you deploy the database schema provided in the sql folder, then change the driver (drvr) to MariaDB. Eventually you may need to configure your user name and password.

Below is an example of configuration call pointing to an MariaDB database called my_gl_database at local.host:

gtoxConf(   drvr = "MariaDB",
            host = "local.host",
            user = "username",
            pass = "********",
            db = "my_gl_database")

Deployed database

The deployed database already contains fully processed study, with

The purpose of the call gtoxLoadAsid() is to list all studies available in the database.

# List available studies
gtoxLoadAsid()

Data and metadata for vignette

In this section we will explore one simple way for loading data in the database. The following chunks prepare the metadata and data in R objects (data.frame) prior database loading.

The following commands loads the data for vignette. The command loads three objects in the environment. The content of each object is described in the following sections. These objects are what users need to prepare before study data can be loaded. In particular the dat object contains the raw data as fetched from the instrument database. This database is only accessible internally to the company, hence its content has been exported and saved in an Rdat object . Some fields, not used by the code, are not reported.

load(system.file("extdata", "data_for_vignette.rda", package="GladiaTOX"))

plate: plate metadata

The plate object stores metadata with plate information.

Most of the columns have self-contained names and content; plate is the plate number (usually an integer); tube is the well location (H1 is row 8 column 1); well_type is the content type of the well (c positive control, t treatment, n is the negative control); endpoint contains assay names with no exposure duration info appended; u_boxtrack is a plate identifier used to join the plate metadata table with the raw data table prior data is loaded in the GladiaTOX database.

print(head(plate), row.names = FALSE)

chnmap: assay metadata and channel mapping

The second metadata table contains assay mapping information. In the example below two assays are shown: Cytotoxicity (TIER1) and DNA damage (pH2AX).

Five endpoints are part of the cytotoxicity assay (e.g., Cell count, membranepermeability). Two endpoints are shown to be part of the DNA damage assay. Since multiple endpoints can be read from the same plate, each of them is read on a separate channel. This column will also be used later on to join meatadata and data tables.

print(head(chnmap, 7), row.names = FALSE)

The content of plate and chnmap are then combined to generate the assay table. In the assay table, assay and endpoint are concatenated to timepoints to generate assays entries for the database.

assay <- buildAssayTab(plate, chnmap)
print(head(assay, 4), row.names = FALSE)

dat: image quantification raw data

The data table is an export from the image quantification instrument.

This table contains the raw fluorescence quantification values: measure_val; rowi and coli are the row and column indexes; machine_name is the channel name and is used to join this table with the assay table above; u_boxtrack is the plate identified and is used to join the table with the plate table.

print(head(dat), row.names = FALSE)

Database loading

In this sections data and metadata will be loaded in the GladiaTOX database. Let's set the study parameters, study name and phase of the new study phase to be loaded in the database and processed.

## Set study parameters
std.nm <- "SampleStudy" # study name
phs.nm <- "PhaseII" # study phase

Register study info in database

The following code will register metadata file content in the database, including: assays, endpoints, treatments and controls. The status of the assay source table (study table) before and after new study creation is displayed below calling gtoxLoadAsid(). The purpose of the call is to list all studies available in the database before and after the new study is added with the function loadAnnot().

## List of studies before loading
gtoxLoadAsid()

## Load annotation in gtoxDB
loadAnnot(plate, assay, NULL)

## List of studies after loading
gtoxLoadAsid()

The loadAnnot function call registers multiple study parameters in the database, including the creation of the new assay source id (asid). The asid identifies the pair study name, study phase. The asid is what will be used to load raw data of the study, process the study and generate reports.

Load raw data in database

The asid just created can be retrieved by querying the database and specify the study name and phase.

# Get assay source ID
asid = gtoxLoadAsid(fld = c("asnm", "asph"), val = list(std.nm, phs.nm))$asid
asid

The asid and the dat objects are the inputs to the prepareDatForDB function used to join metadata stored in database to the raw data stored in the dat object.

Raw data is then loaded in the database with the gtoxWriteData function. Study whose asid is 2 is now ready to be processed.

# Prepare and load data
dat <- prepareDatForDB(asid, dat)
gtoxWriteData(dat[ , list(acid, waid, wllq, rval)], lvl = 0, type = "mc")

Quality control: data processing and reporting

Metadata and data are now registered in the database. Next step is to select the processing methods we want to apply on the data. There are multiple levels of processing (see gtoxLoadMthd(lvl=3) for details). The function assignDefaultMthds is a shortcut to assign all levels methods at once. The methods selected would probably fit well to most users.

assignDefaultMthds(asid = asid)

With the default selection, raw data is normalized by computing the log2 fold change of values in each well against the median of the corresponding controls.

Compute the noise band

The package computes a noise band to discriminate concentration series that are active versus those that are not. To compute the noise band we need to process and normalize vehicle's data running the following code:

# Run level 1 to level 3 functions
res <- gtoxRun(asid = asid, slvl = 1, elvl = 3, mc.cores = 2)

The default behaviour is to compute noise band margins separately for each endpoint. Margins correspond to 3 times the baseline median absolute deviation of vehicle responses. The following code computes the cutoffs and store them in the database.

# Extract assay endpoints ids of the study
aeids <- gtoxLoadAeid(fld = "asid", val = asid)$aeid
# Compute Vehicle Median Absolute deviation
tmp <- mapply(function(xx){
    tryCatch(gtoxCalcVmad(inputs = xx, aeid = xx, 
    notes = "computed within study"), 
    error = function(e) NULL)},
    as.integer(aeids))

Once the database is populated with noise band margins, then all chemical's data can be processed.

# Apply all functions from level 1 to level 6
res <- gtoxRun(asid = asid, slvl = 1, elvl = 6, mc.cores = 2)

In the original work (Filer et al., 2016), the default behaviour is to compute noise band margins based on the response of the lowest two concentrations of the series. That assumes that no response is observed at those concentrations. The current package overcome that assumption and extend the list of functionalities. The database design was modified accordingly.

Quality control report

Quality control is the mean to check the quality of the data produced in the lab. Each experimental plate is controlled. Plates not passing the control step are filtered out. Quality control is commonly based on a visual inspection. The package exposes functionalities to generate a self contained pdf file with plate heatmaps and positive control plots.

## QC report
gtoxReport(type = "qc", asid = asid, report_author = "report author",
report_title = "Vignette QC report", odir = outdir)

An example of plate heatmap is shown below, and is what included in the quality control pdf report. The following code is used to extract the plate id we want to plot.

# Define assay component and extract assay component ID
acnm <- "DNA damage (pH2AX)_DNA damage (pH2AX)_4h"
acid <- gtoxLoadAcid(fld=c("asid", "acnm"), val=list(asid,acnm))[, acid]
# Extract assay plate ID corresponding to plate name S-000031351
apid <- gtoxLoadApid()[u_boxtrack == "S-000031351", apid]
# Load level 2 data (Raw data before normalization)
l2 <- gtoxLoadData(lvl = 2L, fld = "acid", val = acid)

The plate heatmap is performed with the folliwing code.

gtoxPlotPlate(dat = l2, apid = apid, id = acid)

The QC report includes also dose-responses for positive control chemicals as in figure. For that we need to first extract level 4 data.

# Extract assay endpoint ID
aeid <- gtoxLoadAeid(fld = c("acid", "analysis_direction"), 
                        val = list(acid, "up"))[, aeid]
# Extract sample ID
spid <- gtoxLoadWaid(fld = c("apid", "wllt"), 
                        val = list(apid, "c"))[,unique(spid)]
# Collect level 4 data (normalized data)
m4id <- gtoxLoadData(lvl = 4L, fld = c("spid", "aeid"), 
                        val = list(spid, aeid))[, m4id]

Then we can plot the normalized data corresponding to the selected sample ID.

gtoxPlotM4ID(m4id = m4id, lvl = 6, bline = "coff")

The panel on the right side shows a set of information including goodness of fit. In this particular example no info is available since the series has to few concentration to fit a model (4 concentrations is the minimum number to perform a fit).

Data masking

QC report is mainly used to check the quality of the plates. For example, in case the response of a positive control of an assay stays within the noiseband, then the user may decide to filter that plate out. Below is shown the code to mask plate S-000030318.

apid <- gtoxLoadApid()[u_boxtrack%in%"S-000030318", apid] # plate id
waids <- gtoxLoadWaid(fld="apid", val=apid)$waid #well ids
m0ids <- gtoxLoadData(lvl = 0, fld = "waid", val = waids)$m0id # raw data ids
gtoxSetWllq(ids = m0ids, wllq = 0, type = "mc") # set well quality to zero

The masked plate will not be processed and will not be included in the final report.

Data processing and reporting

Process data

Now that the user has selected the processing methods, cutoffs computed, and bad quality plates masked, all information is in place to start processing the data with the following command.

res <- gtoxRun(asid = asid, slvl = 1, elvl = 6, mc.cores = 2)

The gtoxRun returns a list of vectors of logical values used to check processing status. The resulting processed data is automatically stored in the database along with the statistics computed. Statistics include activity concentrations (AC10 and AC50) and minimal effective concentrations (MECs).

Data reporting

The gtoxReport function, with option type = "all", triggers the generation of the full processing report. The pdf file created includes summary tables, dose-response curves (as seen later), and other plots for all chemicals tested in the study.

## Processing report
gtoxReport(type = "all", asid = asid, report_author = "report author",
report_title = "Vignette Processing report", odir = outdir)

Models that best fit the data are also included in the final report. In order to select the best fitting the package evaluate three models: constant, hill and gain-loss. Below is shown an example where all models are fit to the data (ochre, red and blue) from a single plate.

## Endpoint to plot
aeids <- gtoxLoadAeid(fld=c("asid", "aenm"),
val=list(asid, "DNA damage (pH2AX)_DNA damage (pH2AX)_24h_up"),
add.fld="asid")$aeid
## level 4 id to plot
m4id <- gtoxLoadData(lvl=4L)[(aeid==aeids & grepl("chromium", spid))]$m4id[1]
gtoxPlotM4ID(m4id = m4id, lvl = 6, bline = "coff")

The HILL model (marked in red on the right panel) will be selected as best fit since minimizing the Akaike information criteria (AIC).

All winning models are combined into a single plot that is included in the pdf report. An example of winning model plot is shown in figure, for the very same chemical and endpoint used above.

## Get chemical id to plot
chid <- gtoxLoadChem(field = "chnm", val = "chromium",
include.spid = FALSE)$chid
## Plot dose-response curves
gtoxPlotWin(chid = chid, aeid = aeids, bline = "bmad", collapse = TRUE)

The plot shows all replicated dose-response curves. Each curve represents the fitting result on an experimental plate. Only best fits are reported.

Additional reporting plots

Additional reporting plots, not included in the full report, can be obtained as described below. Boxplot of minimal effective concentrations can be obtained running the following chunk. An example of boxplot is reported below. MEC values are shown as dots. Low MECs correspond to high toxicity.

fname <- paste0(format(Sys.Date(), format="%y%m%d"), "_ASID", asid,"_MEC.pdf")
fname <- file.path(outdir, fname)
pdf(fname, width = 11, height = 7)
glPlotStat(asid)
dev.off()
knitr::include_graphics('MECfig.png')

The MEC plot shows an example of MEC boxplot. In the example the GSH assay is shown along with the two endpoints (GSH content and Cell count). Chemicals are listed in the legend to the right. Each dot in the plot represents an MEC value.

MEC values can also be reported in a piechart. Below an example.

chnms <- c("mercury", "o-cresol", "p-cresol")
glPlotPie(asid, chnms = chnms)

The pie plot reports the mean MECs for all endpoints measured in the study. Time points are reported to the right (4h, 24h). Each slice is associated to an endpoint. Numbers on the slides indicate the corresponding MEC means.

Severity scores can also be computed and displayed. This score indicate the average impact of chemicals across multiple endpoints.

glPlotToxInd(asid)

Example of severity score plot reporting the full list of chemicals used in the study; y-axis reports the severity score value (normalized between 0 and 1); x-axis in just the index of the chemical.

Session Info

sessionInfo()


pmpsa-hpc/GladiaTOX documentation built on Sept. 1, 2023, 5:52 p.m.