This snakemake pipeline performs alignment and removal of PCR duplicates from a fastq file.
A sorted .bam
file for each aligned sampled with duplicates marked.
Make sure to install and properly run snakemake, clone this repository and run the snakefile.
All .fastq
files must be inside a folder called fastq
. After that run:
snakemake --snakefile /PATH/TO/SNAKEFILE/bowtie_markdup.smk --cores 60
For paired-end reads, run:
snakemake --snakefile /PATH/TO/SNAKEFILE/bowtie2_markdup_pairend.smk --cores 60
This pipelines uses bowtie2
to align reads to hg38 and sambamba
to mark duplicates.
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