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Computes read coverage across exon-intron, intron-exon and flanking exon-exon junctions for a given .bam file.

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YounisLab/splicing-analysis

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splicing-analysis

Prerequisites

  1. Install docker CE.

Building

docker image build -t splicing-analysis .

Running

Usage: nextflow run splicing-analysis.nf --ref_dir <REF_DIR> --bam_file <BAM_FILE> --junc_bed <JUNCTIONS_BED> ---fpkm <FPKM_FILE> --genome <GENOME_VERSION> --sample_name <OUT_SAMPLE_NAME>

        REF_DIR             Directory containing reference files
        BAM_FILE            BAM file containing reads
        JUNCTIONS_BED       BED file containing junctions
        FPKM_FILE           gene_abund.tab file obtained from stringtie
        GENOME_VERSION      Human Genome version prefix used in REF_DIR files
        OUT_SAMPLE_NAME     Name of output directory

eg: nextflow run splicing-analysis.nf --ref_dir /home/data/hg38_ref/ --bam_file ./accepted_hits.bam --junc_bed ./junctions.bed --fpkm ./gene_abund.tab --genome hg38 --sample_name MCF7

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Computes read coverage across exon-intron, intron-exon and flanking exon-exon junctions for a given .bam file.

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