GSE137258 Processing Pipeline

OTHER code_examples 2 steps

Publication

Inhibition of YTHDF2 triggers proteotoxic cell death in MYC-driven breast cancer.

Molecular cell (2021) — PMID 34216543

Dataset

GSE137258

Inhibition of YTHDF2 triggers proteotoxic cell death in MYC-driven breast cancer

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

    Library strategy: DNA-seq

    FastQC (Inferred with models/gemini-2.5-flash) v0.11.9 (Inferred with models/gemini-2.5-flash) GitHub
    $ Bash example
    # Install FastQC (if not already installed)
    # conda install -c bioconda fastqc
    
    # Define input FASTQ files and output directory
    # Replace with actual paths to your DNA-seq raw data
    READ1="sample_R1.fastq.gz"
    READ2="sample_R2.fastq.gz"
    OUTPUT_DIR="fastqc_results"
    
    # Create output directory if it doesn't exist
    mkdir -p "${OUTPUT_DIR}"
    
    # Run FastQC on the raw DNA-seq FASTQ files
    # This performs quality control checks on the sequencing data
    fastqc "${READ1}" "${READ2}" -o "${OUTPUT_DIR}"
  2. 2

    CRISPR screening data was aligned and processed using MaGeCK.

    MaGeCK v0.5.9.3
    $ Bash example
    # Install MaGeCK (if not already installed)
    # conda install -c bioconda mageck
    
    # Example: Perform MaGeCK analysis for gene essentiality testing.
    # This assumes 'sgRNA_counts.txt' contains read counts for sgRNAs across samples,
    # 'sgRNA_library.txt' maps sgRNAs to target genes, and 'design_matrix.txt'
    # specifies control and treatment samples. Replace placeholder file names and paths
    # with actual data.
    
    # Example content for sgRNA_counts.txt (tab-separated):
    # sgRNA_ID\tSample1_Control\tSample2_Control\tSample3_Treatment\tSample4_Treatment
    # sgRNA1\t100\t120\t50\t60
    # sgRNA2\t200\t210\t180\t190
    # ...
    
    # Example content for sgRNA_library.txt (tab-separated):
    # sgRNA_ID\tGene_ID
    # sgRNA1\tGeneA
    # sgRNA2\tGeneB
    # ...
    
    # Example content for design_matrix.txt (tab-separated):
    # Sample_ID\tCondition
    # Sample1_Control\tcontrol
    # Sample2_Control\tcontrol
    # Sample3_Treatment\ttreatment
    # Sample4_Treatment\ttreatment
    
    mageck test \
        -k sgRNA_counts.txt \
        -l sgRNA_library.txt \
        -n mageck_results \
        -d design_matrix.txt \
        --control-id control \
        --treatment-id treatment
Raw Source Text
Library strategy: DNA-seq
CRISPR screening data was aligned and processed using MaGeCK.
Genome_build: hg19
Supplementary_files_format_and_content: MaGeCK processed gene summary
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