GSE68172 Processing Pipeline

GSE code_examples 2 steps

Publication

An in vivo genome-wide CRISPR screen identifies the RNA-binding protein Staufen2 as a key regulator of myeloid leukemia.

Nature cancer (2020) — PMID 34109316

Dataset

GSE68172

LAA expression profiles on LSC compared to other tissues

Warning: Pipeline descriptions and code snippets may be inferred or AI-generated. Use them only as a starting point to guide analysis, and validate before use.
  1. 1

    The data were analyzed with BRB ArrayTools using RMA.

    BRB ArrayTools vNot specified (Inferred with models/gemini-2.5-flash) GitHub
    $ Bash example
    # BRB ArrayTools is primarily a GUI-based software for microarray data analysis.
    # Direct command-line execution for specific analysis steps like RMA (Robust Multi-array Average)
    # is not typically performed via a single bash command like other CLI tools.
    # Users interact with the software through its graphical interface to load raw microarray data (e.g., .CEL files),
    # select analysis methods (e.g., RMA for normalization), and view results.
    
    # Installation (conceptual - typically involves downloading and installing a GUI application):
    # For Windows/macOS, download the installer from the official BRB ArrayTools website.
    # Example of a conceptual command if it were a CLI tool (this is NOT how BRB ArrayTools is used):
    # brb_arraytools --method RMA --input raw_microarray_data.CEL --output normalized_data.txt
    # The analysis is performed interactively within the GUI, where RMA is selected as a normalization method.
  2. 2

    Intensity values were log2 transformed

    R (Inferred with models/gemini-2.5-flash) vbase function
    $ Bash example
    # Install R if not already installed (example for Debian/Ubuntu)
    # sudo apt-get update && sudo apt-get install -y r-base
    
    # Assuming input data is in a tab-separated file (input.tsv)
    # and intensity values are in a column named 'Intensity'.
    # This script will add a new column 'Intensity_log2'.
    
    # Create a dummy input file for demonstration (replace with your actual input.tsv)
    # echo -e "Sample\tIntensity\tOtherData" > input.tsv
    # echo -e "S1\t100\tA" >> input.tsv
    # echo -e "S2\t250\tB" >> input.tsv
    # echo -e "S3\t50\tC" >> input.tsv
    # echo -e "S4\t1000\tD" >> input.tsv
    
    Rscript -e '
      # Read the input data
      data <- read.delim("input.tsv", header = TRUE, sep = "\t")
      
      # Perform log2 transformation on the "Intensity" column
      # Ensure the column exists and contains numeric values
      if ("Intensity" %in% colnames(data)) {
        data$Intensity_log2 <- log2(data$Intensity)
      } else {
        stop("Column 'Intensity' not found in the input file.")
      }
      
      # Write the transformed data to a new output file
      write.table(data, "output_log2.tsv", sep = "\t", row.names = FALSE, quote = FALSE)
    '
    
    # To view the output file:
    # cat output_log2.tsv
Raw Source Text
The data were analyzed with BRB ArrayTools using RMA. Intensity values were log2 transformed
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