erssa {ERSSA} | R Documentation

## Empirical RNA-seq Sample Size Analysis

### Description

ERSSA is a package designed to test whether an currently available RNA-seq dataset has sufficient biological replicates to detect a majority of differentially expressed (DE) genes between two conditions. Base on the number of biological replicates available, the algorithm subsamples at step-wise replicate levels and uses existing differentially expression analysis softwares (e.g. edgeR and DESeq2) to identify the number of DE genes. This process is repeated for a given number of times with unique combinations of samples to generate a distribution of DE genes at each replicate level. Compare to existing RNA-seq sample size analysis algorithms, ERSSA does not rely on any a priori assumptions about the dataset, but rather uses an user-supplied pilot RNA-seq dataset to determine whether the current replicate level is sufficient to detect a majority of DE genes.

### Usage

    erssa(
      count_table = NULL,
      condition_table = NULL,
      DE_ctrl_cond = NULL,
      filter_cutoff = 1,
      counts_filtered = FALSE,
      comb_gen_repeat = 30,
      DE_software = "edgeR",
      DE_cutoff_stat = 0.05,
      DE_cutoff_Abs_logFC = 1,
      DE_save_table = FALSE,
      marginalPlot_stat = "median",
      TPR_FPR_stat = "mean",
      path = ".",
      num_workers = 1,
      save_log = FALSE,
      save_plot = TRUE
    )

### Arguments

`count_table` | A RNA-seq count matrix with genes on each row and samples on each column. If count_table has already been filtered to remove non- or low-expressing genes, then counts_filtered argument should be changed to TRUE.
`condition_table` | A condition table with two columns and each sample as a row. Column 1 contains sample names and Column 2 contains sample conditions (e.g. Control, Treatment).
`DE_ctrl_cond` | The name of control condition in the comparison. Must be one of the two conditions in the condition table.
`filter_cutoff` | The average CPM threshold set for filtering genes. Default to 1.
`counts_filtered` | Boolean. Whether count table has already been filtered. Default = FALSE with the function run filtering by average CPM at the cutoff specified by filter_cutoff value.
`comb_gen_repeat` | The number of maximum unique combinations to generate at each replicate level. More tests will be performed with a bigger value, but run time also increases linearly. Default set to 30 unique combinations at maximum.
`DE_software` | The name of DE analysis software to use. Current options include "edgeR" and "DESeq2". Default to "edgeR".
`DE_cutoff_stat` | The cutoff in FDR or adjusted p-value used to determine whether a gene is differentially expressed. Genes with lower FDR or adjusted p-value pass the cutoff. Default = 0.05.
`DE_cutoff_Abs_logFC` | The cutoff in abs(log2FoldChange) for differential expression consideration. Genes with higher abs(log2FoldChange) pass the cutoff. Default = 1.
`DE_save_table` | Boolean. The results of differential expression tests can be saved to the drive for further analysis. Default setting does not save the results to save drive space. Default = FALSE.
`marginalPlot_stat` | The statistic used for plotting of values in marginal plot function. Options include 'mean', 'median'. Default='median'.
`TPR_FPR_stat` | The statistics used to summarize TPR and FPR at each replicate level in ggplot2_TPR_FPRPlot function. Options include 'mean', 'median'. Default = 'mean'.
`path` | The path to which the plots and results will be saved. Default to current working directory.
`num_workers` | Number of nodes to use for parallel computing the DE tests
`save_log` | Boolean. Whether to save runtime parameters in log file. Defualt to false.
`save_plot` | Boolean. Wehther to save ggplot2 plots to drive. Default to true.

### Details

`erssa` function is a wrapper that calls several ERSSA functions in sequence. For additional description of the functions called, please see their respective manual.

For the majority of current RNA-seq analysis, RNA-seq samples are aligned to the reference, followed by running quantification packages to generate count tables. ERSSA can then take the unfiltered count table and remove non- to low-expressing genes with count_filter function. Alternatively, a filtered count table can be supplied and filtering will be skipped.

Next, unique combinations of samples at various biological replicate levels will be generated by comb_gen function and passed to a differential expression analysis software for statistical testing for DE genes. The pipeline currently supports edgeR and DESeq2, but additional software support can be easily added.

The generated differential expression results are then analyzed by several plotting functions briefly described here. ggplot2_dotplot function plots the trend in DE gene identification. ggplot2_marginPlot function plots the marginal change in the number of DE genes as replicate level increases. ggplot2_intersectPlot function plots the number of DE genes that is common across combinations. ggplot2_TPR_FPRPlot function plots the TPR and FPR of DE detection using the full dataset's list of DE gene as the ground truth. Base on insights from these plots, the user can determine whether a desirable level of DE gene discovery has been reached.

At the default setting, the results of statistical tests are not saved, only the list of DE genes is. However, all of the test results can be optionally saved for further analysis.

At default setting, only one CPU node is employed and depend on the number of tests that needs to be done, the calculations can take some time to complete. If additional nodes are available, additional nodes can be employed by specifying the num_workers argument. Parallel computing requires BiocParallel package.

The results including list of DE genes and ggplot2 objects are returned. All runtime parameters can optionally be saved in a log file named "erssa.log".

### Value

A list of objects generated during the analysis is returned:

- count_table.filteredfiltered count table

- samp.name.combthe samples involved in each statistical test

- list.of.DE.geneslist of DE genes in each statistical test

- gg.dotplot.obja list of objects that can be used to recreate the dot plot. See function ggplot2_dotplot manual for more detail.

- gg.marinPlot.obja list of objects that can be used to recreate the marginal num. of DE genes plot. See function ggplot2_marginPlot manual for more detail.

- gg.intersectPlot.obja list of objects that can be used to recreate the num. of intersect genes plot. See function ggplot2_intersectPlot manual for more detail.

- gg.TPR_FPRPlot.obja list of objects that can be used to recreate the TPR vs. FPR plot. See function ggplot2_TPR_FPRPlot manual for more detail.

### Author(s)

Zixuan Shao, Zixuanshao.zach@gmail.com

### References

Ching, Travers, Sijia Huang, and Lana X. Garmire. “Power Analysis and Sample Size Estimation for RNA-Seq Differential Expression.” RNA, September 22, 2014. https://doi.org/10.1261/rna.046011.114.

Hoskins, Stephanie Page, Derek Shyr, and Yu Shyr. “Sample Size Calculation for Differential Expression Analysis of RNA-Seq Data.” In Frontiers of Biostatistical Methods and Applications in Clinical Oncology, 359–79. Springer, Singapore, 2017. https://doi.org/10.1007/978-981-10-0126-0_22.

### Examples

    # load example dataset containing 1000 genes, 4 replicates and 5 comb. per
    # rep. level
    data(condition_table.partial, package = "ERSSA")
    data(count_table.partial, package = "ERSSA")

    # run erssa with the "partial" dataset, use default edgeR for DE
    ssa = erssa(count_table.partial, condition_table.partial,
                DE_ctrl_cond='heart')

    # run erssa with the "full" dataset containing 10 replicates per heart and
    # muscle, all genes included.
    # Remove comments to run
    #   set.seed(1)
    #   data(condition_table.full, package="ERSSA")
    #   data(count_table.full, package="ERSSA")
    #   ssa = erssa(count_table.full, condition_table.full, DE_ctrl_cond='heart')

[Package ERSSA version 1.6.0 Index]