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snakeflow

RNA-Seq and ChIP-seq workflow based on snakemake

Dependency

  • python 3

    • numpy
    • pandas
    • snakemake
    • matplotlib
    • seaborn
    • gseapy
  • hisat2, salmon

  • samtools, deeptools, bedtools

  • rMATS-turbo, rmats2sashimiplot

  • fastqc, rseqc, multiqc

  • graphviz

  • R

    • DESeq2
    • tximport
    • readr
    • pheatmap
    • ggplot2
    • ggrepel
    • clusterProfiler
    • ChIPSeeker
    • EnsDb.Hsapiens.v86

Installation

Set up running environment. This config file will create a python 3.x env.

bash snakeflow-enviroment-setup.sh

usage

# Step1: activate snakemake
source activate snakeflow

# Step2: clone this repo

# Step3: copy all your fastq files into fastq dir
find . -name "*fastq.gz" | while read id; do cp $id fastq/; done;

# Step4: modify config.yml with your own paramter
# Note: put config.yml in the same dir with your snakefile.
vim  config.yml

# Step5: run snakemake with -np option. this test your ``commands`` runs without any errors.
snakemake -s salmon-tximport-deseq2-v0.2.snakefile -np

# Step6: export workflow charts
snakemake -s salmon-tximport-deseq2-v0.2.snakefile --dag | dot -Tpdf > dag.pdf

# Step7: or using the default snakemake environment you've created above.
snakemake -s salmon-tximport-deseq2-v0.1.snakefile -p -j 8

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RNA-seq workflow based on snakemake

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  • Python 91.2%
  • R 8.3%
  • Shell 0.5%