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
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.
Processing Steps
Generate Jupyter Notebook-
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
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