GSE27218 Processing Pipeline

RNA-Seq code_examples 1 step

Publication

Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43.

Nature neuroscience (2011) — PMID 21358643

Dataset

GSE27218

Disrupted processing of long pre-mRNAs and widespread RNA missplicing are components of neuronal vulnerability from loss of nuclear TDP-43 (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

    Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to mm8 whole genome using bowtie v0.12.2 with parameters -q -p 4 -e 100 -y -a -m 10 --best --strata

    Bowtie v0.12.2 GitHub
    $ Bash example
    # Install Bowtie v0.12.2 if not already installed
    # conda install -c bioconda bowtie=0.12.2
    
    # Ensure the mm8 index is available. This typically involves downloading pre-built indices
    # or building them from the mm8 reference genome FASTA using 'bowtie-build mm8.fa mm8_index'.
    # Replace 'mm8_index' with the actual path to your Bowtie index for mm8.
    # Replace 'reads.fastq' with the path to your pre-processed (trimmed and masked) sequenced reads.
    # The output 'alignment.sam' will contain the alignments.
    bowtie -q -p 4 -e 100 -y -a -m 10 --best --strata mm8_index reads.fastq > alignment.sam
Raw Source Text
Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to mm8 whole genome using bowtie v0.12.2 with parameters -q -p 4 -e 100 -y -a -m 10 --best --strata
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