# GRmetrics: an R package for calculation and visualization of dose-response metrics based on growth rate inhibition

Nicholas Clark

#### 4 January 2019

# Contents

# 1 Background

Quantifying drug response is the cornerstone of many pharmacological experiments ranging from pharmacogenomics studies to small-scale analyses of drug resistance. In general, cells are grown in the presence or absence of drugs for a few days and the endpoint cell count values (or a surrogate) is compared. From the relative cell count, metrics of drug sensitivity such as IC50 or Emax values are evaluated. In cases where the untreated control cells grow over the course of the assay, these traditional metrics are confounded by the number of divisions that take place over the course of an assay. In particular, for drugs that impact growth rate and block cell division, slow-growing cell lines will appear more resistant than fast-growing lines although the biological effect on a per-division basis may be the same.

Hafner et al. recently proposed alterative drug-response metrics based on growth rate inhibition (GR metrics) that are robust to differences in nominal division rate and assay duration. Using these metrics requires only to know the number of cells (or a surrogate) at the time of treatment; note that this value may also be inferred from the nominal division rate and the value of an untreated sample at the endpoint.

To facilitate the use of these GR metrics, we have developed an R package that provides functions to analyze and visualize drug response data with these new metrics across multiple conditions and cell lines.

# 2 Installation

The GRmetrics package can be installed through Bioconductor

    if (!requireNamespace("BiocManager", quietly=TRUE))
        install.packages("BiocManager")
    BiocManager::install("GRmetrics")

#References: Hafner, M., Niepel, M. Chung, M. and Sorger, P.K., Growth Rate Inhibition Metrics Correct For Confounders In Measuring Sensitivity To Cancer Drugs. Nature Methods 13.6 (2016): 521-527. (http://dx.doi.org/10.1038/nmeth.3853)

Corresponding MATLAB and Python scripts available on repo:

https://github.com/sorgerlab/gr50_tools.

Note: Most, but not all of these scripts have been reproduced in this R package. Namely, this package does not contain code for “Case B” of the MATLAB scripts nor does it contain an R script to generate the example input data. The python script for generating the example data can be found in the “inst/scripts/” directory.

Browser interface and online tools: http://www.grcalculator.org

Much of the description below has been adapted from:

https://github.com/datarail/gr_metrics/blob/master/README.md.

#Input data The main function of the package is GRfit, which takes in a data frame containing information about concentration, cell counts over time, and additional grouping variables for a dose-response assay and calculates growth-rate inhibition (GR) metrics for each experiment in the dataset.

There are two cases of data input accepted by the GRfit function. They are described in detail below. Case “A” is the default option.

##Case A: a single file with control values assigned to treated measurements The control values (both control and time 0 cell counts) are pre-computed by the user and assigned to each treatment (row) in appropriate columns in the input file. Control cell counts should be in a column labeled cell_count__ctrl and the time 0 cell counts in a column labeled cell_count__time0.

An example input data frame for “Case A”, named “inputCaseA”, is contained within the package. To access it, use the following code:

    library(GRmetrics)
    data(inputCaseA)

The mandatory inputs for Case “A” are:

- inputData - the name of an input data frame with the following columns as well as other grouping columns
  1. concentration - column with concentration values (not log transformed) of the perturbagen on which dose-response curves will be evaluated
  2. cell_count - column with the measure of cell number (or a surrogate of cell number) after treatment
  3. cell_count__time0 - column with initial (Time 0) cell counts - the measure of cell number in untreated wells grown in parallel until the time of treatment
  4. cell_count__ctrl - column with the Control cell count: the measure of cell number in control (e.g. untreated or DMSO-treated) wells from the same plate

All other columns will be treated as additional keys on which the data will be grouped (e.g. cell_line, drug, time, replicate)

##Case C: a single file with control values stacked with treated measurements In the most general case, the control cell counts are in the same file and format as the treated cell counts. Control cell counts will be averaged (using a 50%-trimmed mean) and automatically matched to the treated cell counts based on the keys (columns in the data file). The control cell count values must have a value of 0 for concentration and a value for time that matches the treated measurements. The time 0 cell count values must have value of 0 for time. If the structure of the data is complex, the provided scripts may inappropriately match control and treated cell counts, so users instead should format their data as described in case A.

An example input data frame for “Case C”, named “inputCaseC”, is contained within the package. To access it, use the following code:

    library(GRmetrics)
    data(inputCaseC)

The mandatory inputs for Case “C” are:

- inputData - the name of an input data frame with the following columns as well as other grouping columns
  1. concentration - column with concentration values (not log transformed) of the perturbagen on which dose-response curves will be evaluated
  2. cell_count - column with the measure of cell number (or a surrogate of cell number)
  3. time - column with the time at which a cell count is observed

All other columns will be treated as additional keys on which the data will be grouped (e.g. cell_line, drug, replicate)

##Functions The package contains 3 visualization functions: GRdrawDRC, GRscatter, and GRbox.

All of these functions take in an object created by GRfit as well as additional arguments. The results can be viewed in a static ggplot image or an interactive plotly (turned on/off by the plotly parameter).

- GRdrawDRC this function draws the (growth-rate inhibition) dose-response curve using the parameters calculated by the GRfit function. If points is set to TRUE, then it will also plot the points used to fit each curve.
- GRscatter this function draws a scatterplot of a given GR metric (GR50, GRmax, etc.) with the xaxis value(s) plotted against the yaxis value(s).
- GRbox this function draws boxplots of a given GR metric (GR50, GRmax, etc.) for values of a given grouping variable. It overlays the points used to make these boxplots and can color them according to another grouping variable.

The package also contains 4 accessor functions, which extract data from the SummarizedExperiment object created by GRfit. These functions are: GRgetMetrics, GRgetDefs, GRgetValues, and GRgetGroupVars.

- GRgetMetrics this function returns a table of GR metrics and traditional metrics along with goodness of fit measures. It also identifies each fit as flat or sigmoidal.
- GRgetDefs this function returns a table containing the definition of each GR metric, traditional metric, and goodness of fit measure calculated.
- GRgetValues this function returns a table of the original data (in the form of “Case A”) with columns for GR values and relative cell counts.
- GRgetGroupVars this function returns a vector of the grouping variables used to create the object. These are the variables in the dataset that are not averaged over.

# 3 Examples

Load example data (Case A)

    data(inputCaseA)

    head(inputCaseA)

    ##   cell_line agent perturbation replicate time concentration cell_count
    ## 1    MCF10A drugA            0         1   48      0.001000       1131
    ## 2    MCF10A drugA            0         1   48      0.003162       1205
    ## 3    MCF10A drugA            0         1   48      0.010000       1021
    ## 4    MCF10A drugA            0         1   48      0.031620        743
    ## 5    MCF10A drugA            0         1   48      0.100000        459
    ## 6    MCF10A drugA            0         1   48      0.316200        318
    ##   cell_count__ctrl cell_count__time0
    ## 1           1212.5             299.5
    ## 2           1212.5             299.5
    ## 3           1212.5             299.5
    ## 4           1212.5             299.5
    ## 5           1212.5             299.5
    ## 6           1212.5             299.5

Calculate GR values and solve for GR metrics parameters (i.e. fit curves)

    drc_output = GRfit(inputCaseA, groupingVariables = c('cell_line','agent'))

See overview of output data (SummarizedExperiment object)

    drc_output

    ## class: SummarizedExperiment
    ## dim: 19 12
    ## metadata(2): '' ''
    ## assays(1): ''
    ## rownames(19): ctrl_cell_doublings GR50 ... pval_rel_cell
    ##   flat_fit_rel_cell
    ## rowData names(2): Metric Description
    ## colnames(12): BT20 drugA BT20 drugB ... MCF7 drugC MCF7 drugD
    ## colData names(6): cell_line agent ... experiment
    ##   concentration_points

Review output table of GR metrics parameters

    head(GRgetMetrics(drc_output))

    ##              cell_line agent  fit_GR fit_rel_cell   experiment
    ## BT20 drugA        BT20 drugA sigmoid      sigmoid   BT20 drugA
    ## BT20 drugB        BT20 drugB    flat         flat   BT20 drugB
    ## BT20 drugC        BT20 drugC sigmoid      sigmoid   BT20 drugC
    ## BT20 drugD        BT20 drugD sigmoid      sigmoid   BT20 drugD
    ## MCF10A drugA    MCF10A drugA sigmoid      sigmoid MCF10A drugA
    ## MCF10A drugB    MCF10A drugB sigmoid      sigmoid MCF10A drugB
    ##              concentration_points ctrl_cell_doublings       GR50       GRmax
    ## BT20 drugA                      9            1.256578 0.09080477  0.03305683
    ## BT20 drugB                      9            1.256578        Inf  0.99059876
    ## BT20 drugC                      9            1.256578 0.24800535 -0.71018761
    ## BT20 drugD                      9            1.256578 0.02215168 -0.05039563
    ## MCF10A drugA                    9            2.121869 0.03964474 -0.06533159
    ## MCF10A drugB                    9            2.121869 1.73502043  0.05502585
    ##                  GR_AOC      GEC50       GRinf      h_GR        r2_GR
    ## BT20 drugA   0.50926262 0.08715113  0.02267627 1.1301507  0.968621411
    ## BT20 drugB   0.02209509 0.00000000  0.99059876 0.0100000 -0.004378014
    ## BT20 drugC   0.56226401 0.58512184 -0.78533762 1.0999555  0.977472706
    ## BT20 drugD   0.67647820 0.02363744 -0.04032884 1.1948823  0.976877384
    ## MCF10A drugA 0.62559226 0.04496553 -0.06702646 0.9988893  0.986610798
    ## MCF10A drugB 0.22076112 2.41459967 -0.18764416 0.9641440  0.971364003
    ##                   pval_GR flat_fit_GR       IC50      Emax       AUC
    ## BT20 drugA   2.096868e-80          NA 0.55085523 0.4482145 0.7052483
    ## BT20 drugB   1.000000e+00   0.9757885        Inf 0.9864435 0.9847035
    ## BT20 drugC   4.938309e-88          NA 0.56550564 0.1029963 0.6905482
    ## BT20 drugD   1.967703e-87          NA 0.09308940 0.4062678 0.6118821
    ## MCF10A drugA 2.731585e-66          NA 0.05331866 0.2166405 0.5080238
    ## MCF10A drugB 9.815911e-55          NA 2.27507203 0.2721915 0.8128093
    ##                    EC50       Einf        h r2_rel_cell pval_rel_cell
    ## BT20 drugA   0.08039928 0.44184478 1.117968  0.88748193  5.185369e-51
    ## BT20 drugB   0.00000000 0.98644353 0.010000 -0.01158457  1.000000e+00
    ## BT20 drugC   0.49386992 0.07154552 1.140094  0.98373427  1.575768e-95
    ## BT20 drugD   0.02197710 0.41098367 1.195509  0.88438881  2.182698e-50
    ## MCF10A drugA 0.03076491 0.21427553 1.017582  0.94713334  2.048170e-45
    ## MCF10A drugB 1.56574961 0.15621884 1.002558  0.96108795  4.497222e-50
    ##              flat_fit_rel_cell
    ## BT20 drugA                  NA
    ## BT20 drugB           0.9834633
    ## BT20 drugC                  NA
    ## BT20 drugD                  NA
    ## MCF10A drugA                NA
    ## MCF10A drugB                NA

View descriptions of each GR metric (or goodness of fit measure)

    View(GRgetDefs(drc_output))

Review output table of GR values

    head(GRgetValues(drc_output))

    ##   cell_line agent perturbation replicate time concentration cell_count
    ## 1    MCF10A drugA            0         1   48      0.001000       1131
    ## 2    MCF10A drugA            0         1   48      0.003162       1205
    ## 3    MCF10A drugA            0         1   48      0.010000       1021
    ## 4    MCF10A drugA            0         1   48      0.031620        743
    ## 5    MCF10A drugA            0         1   48      0.100000        459
    ## 6    MCF10A drugA            0         1   48      0.316200        318
    ##   cell_count__ctrl cell_count__time0 log10_concentration    GRvalue
    ## 1           1212.5             299.5          -3.0000000 0.93219264
    ## 2           1212.5             299.5          -2.5000381 0.99385806
    ## 3           1212.5             299.5          -2.0000000 0.83663626
    ## 4           1212.5             299.5          -1.5000381 0.56891172
    ## 5           1212.5             299.5          -1.0000000 0.23569217
    ## 6           1212.5             299.5          -0.5000381 0.03015641
    ##   rel_cell_count ctrl_cell_doublings   experiment
    ## 1      0.9327835            2.017357 MCF10A drugA
    ## 2      0.9938144            2.017357 MCF10A drugA
    ## 3      0.8420619            2.017357 MCF10A drugA
    ## 4      0.6127835            2.017357 MCF10A drugA
    ## 5      0.3785567            2.017357 MCF10A drugA
    ## 6      0.2622680            2.017357 MCF10A drugA

View grouping variables used for calculation

    GRgetGroupVars(drc_output)

    ## [1] "cell_line" "agent"

You can also export your results. Here are two examples:

    # Write GR metrics parameter table to tab-separated text file
    write.table(GRgetMetrics(drc_output), file = "filename.tsv", quote = FALSE,
    sep = "\t", row.names = FALSE)
    # Write original data plus GR values to comma-separated file
    write.table(GRgetValues(drc_output), file = "filename.csv", quote = FALSE,
    sep = ",", row.names = FALSE)

#Visualizations You can draw GR dose-response curves with plotly or with ggplot2. You can also specify the range of the graph.

    # Draw dose-response curves
    GRdrawDRC(drc_output)

    GRdrawDRC(drc_output, experiments = c('BT20 drugA', 'MCF10A drugA',
                                          'MCF7 drugA'))

    GRdrawDRC(drc_output, experiments = c('BT20 drugA', 'MCF10A drugA',
                                          'MCF7 drugA'),
              min = 10^(-4), max = 10^2)

    GRdrawDRC(drc_output, plotly = FALSE)

You can also draw scatterplots and boxplots of GR metrics with plotly or ggplot2. Here is an example using example data in the format of Case C.

    ## Case C (scatterplot and boxplot examples)
    data(inputCaseC)

    head(inputCaseC)

    ##   cell_line agent perturbation replicate time concentration cell_count
    ## 1    MCF10A     -            0       NaN    0             0        294
    ## 2    MCF10A     -            0       NaN    0             0        318
    ## 3    MCF10A     -            0       NaN    0             0        287
    ## 4    MCF10A     -            0       NaN    0             0        296
    ## 5    MCF10A     -            0       NaN    0             0        291
    ## 6    MCF10A     -            0       NaN    0             0        286

    output1 = GRfit(inputData = inputCaseC, groupingVariables =
    c('cell_line','agent', 'perturbation', 'replicate', 'time'), case = "C")

    # Draw scatterplots
    GRscatter(output1, 'GR50', 'agent', c('drugA','drugD'), 'drugB')

    ## Coordinate system already present. Adding new coordinate system, which will replace the existing one.

    GRscatter(output1, 'GR50', 'agent', c('drugA','drugD'), 'drugB',
              plotly = FALSE)

    ## Coordinate system already present. Adding new coordinate system, which will replace the existing one.

    # Draw boxplots
    GRbox(output1, metric ='GRinf', groupVariable = 'cell_line',
          pointColor = 'agent')

    GRbox(output1, metric ='GRinf', groupVariable = 'cell_line',
          pointColor = 'agent',
          factors = c('BT20', 'MCF10A'))

    GRbox(output1, metric ='GRinf', groupVariable = 'cell_line',
          pointColor = 'agent',
          factors = c('BT20', 'MCF10A'), plotly = FALSE)

    GRbox(output1, metric ='GR50', groupVariable = 'cell_line',
          pointColor = 'agent', wilA = 'BT20', wilB = c('MCF7', 'MCF10A'),
          plotly = FALSE)

#GR metric details We have developed scripts to calculate normalized growth rate inhibition (GR) values and corresponding metrics (GR50, GRmax, …) based on cell counts measured in dose-response experiments. Users provide a tab-separated data file in which each row represents a separate treatment condition and the columns specify the keys that define the treatment condition (e.g. cell line, drug or other perturbagen, perturbagen concentration, treatment time, replicate) and the measured cell counts (or surrogate). The experimentally measured cell counts that are required for GR metric calculation are as follows: - measured cell counts after perturbagen treatment (cell_count, x(c)) - measured cell counts of control (e.g. untreated or DMSO-treated) wells on the same plate (cell_count__ctrl, x_ctrl) - measured cell counts from an untreated sample grown in parallel until the time of treatment (cell_count__time0, x_0)

The provided GR scripts compute over the user’s data to calculate GR values individually for each treatment condition (cell line, time, drug, concentration, …) using the formula:

    GR(c) = 2 ^ ( log2(x(c)/x_0) / log2(x_ctrl/x_0) ) - 1

Based on a set of GR values across a range of concentrations, the data are fitted with a sigmoidal curve:

    GR(c) = GRinf + (1-GRinf)/(1 + (c/(GEC50))^Hill )

The following GR metrics are calculated:

- GR50, the concentration at which the effect reaches a GR value of 0.5 based on interpolation of the fitted curve.

- GRmax, the effect at the highest tested concentration. Note that GRmax can differ from GRinf if the dose-response does not reach its plateau value. For robustness, we take this as the minimum mean GR value at the two highest concentrations.

- GR_AOC, the area over the dose-response curve, which is the integral of 1-GR(c) over the range of concentrations tested, normalized by the range of concentration.

- GEC50, the drug concentration at half-maximal effect, which reflects the potency of the drug.

- GRinf, GR(c->inf), which reflects asymptotic drug efficacy.

- h_GR, The Hill coefficient of the fitted (GR) curve, which reflects how steep the dose response curve is

- r2_GR, The coefficient of determination - essentially how well the (GR) curve fits to the data points

- pval_GR, The p-value of the F-test comparing the fit of the (GR) curve to a horizontal line fit

- flat_fit_GR, For data that doesn’t significantly fit better to a curve than a horizontal line fit (p > 0.05), the y value (GR) of the flat line

The following traditional metrics are calculated:

- IC50, The concentration at which relative cell count = 0.5

- Emax, The maximal effect of the drug (minimal relative cell count value). For robustness, we take this as the minimum mean relative cell count at the two highest concentrations.

- AUC, The ‘Area Under the Curve’ - The area below the fitted (traditional) dose response curve

- EC50, The concentration at half-maximal effect (not growth rate normalized)

- Einf, The asymptotic effect of the drug (not growth rate normalized)

- h, The Hill coefficient of the fitted (traditional) dose response curve, which - reflects how steep the dose response curve is

- r2_rel_cell, The coefficient of determination - essentially how well the (traditional) curve fits to the data points

- pval_rel_cell, The p-value of the F-test comparing the fit of the (traditional) curve to a horizontal line fit

- flat_fit_rel_cell, For data that doesn’t significantly fit better to a curve than a horizontal line fit (p > 0.05), the y value (relative cell count) of the flat line

In addition to the metrics, the scripts report the r-squared of the fit and evaluate the significance of the sigmoidal fit based on an F-test. If the fit is not significant (p > 0.05), the sigmoidal fit is replaced by a constant value (flat fit). This can be circumvented by using the “force” option in the GRfit function. Additional information and considerations are described in the supplemental material of the manuscript referred above.