GSE276986 Processing Pipeline

RNA-Seq code_examples 1 step

Publication

Neuronal aging causes mislocalization of splicing proteins and unchecked cellular stress.

Nature neuroscience (2025) — PMID 40456907

Dataset

GSE276986

Aging-linked deterioration of RNA metabolism destabilizes the stress response of neurons [RNA-seq]

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

    RNA-Seq data was processed using the NF-Core architecture, which compiles several RNA-seq processing steps into a single executable command

    Nextflow vLatest stable version (Inferred with models/gemini-2.5-flash) GitHub
    $ Bash example
    # Install Nextflow (if not already installed)
    # For example, using Conda:
    # conda install -c bioconda -c conda-forge nextflow
    # Or via curl:
    # curl -s https://get.nextflow.io | bash
    # mv nextflow /usr/local/bin/
    
    # Install nf-core (if not already installed)
    # pip install nf-core
    
    # Create a dummy samplesheet.csv (replace with your actual data)
    # This is a minimal example. Refer to nf-core/rnaseq documentation for full samplesheet format.
    cat <<EOF > samplesheet.csv
    sample,fastq_1,fastq_2,group,replicate
    control_rep1,data/control_rep1_R1.fastq.gz,data/control_rep1_R2.fastq.gz,control,1
    treated_rep1,data/treated_rep1_R1.fastq.gz,data/treated_rep1_R2.fastq.gz,treated,1
    EOF
    
    # Ensure you have a Nextflow compatible container engine (e.g., Docker, Singularity) installed and running.
    # For a full list of available genomes, check: https://nf-co.re/rnaseq/usage#--genome
    # For custom genomes, provide --fasta and --gtf files.
    # Using a recent stable release (e.g., 3.14.0) as an example for the pipeline version.
    nextflow run nf-core/rnaseq \
        -profile docker \
        --input samplesheet.csv \
        --genome GRCh38 \
        --outdir results \
        -r 3.14.0
Raw Source Text
RNA-Seq data was processed using the NF-Core architecture, which compiles several RNA-seq processing steps into a single executable command
Assembly: hg38
Supplementary files format and content: Feature counts for all detected transcripts in .csv format
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