A Nextflow pipeline to perform quality control of sequencing data.
Path to the folder where the FASTQ files are located.
--input /cluster/work/nme/data/josousa/project/fastq/*fastq.gz
Output directory where the files will be saved.
--outdir /cluster/work/nme/data/josousa/project
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Option to force the pipeline to assign input as single-end.
--single_end
By default, the pipeline detects whether the input files are single-end or paired-end.
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Option to provide a custom FastQ Screen config file.
# Default --fastq_screen_conf '/cluster/work/nme/software/config/fastq_screen.conf'
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Option to pass the flag --bisulfite to FastQ Screen.
--bisulfite
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Option to choose the sequencing method. This will adapt the default parameters to the method.
# PBAT --seq_method 'PBAT' # RRBS --seq_method 'RRBS' # Single-cell --seq_method 'Single-cell'
The default parameters for each sequencing method.
# PBAT fastq_screen_args='--bisulfite' trim_galore_args='--clip_R1 9 --clip_R2 9' # RRBS fastq_screen_args='--bisulfite' trim_galore_args='--rrbs' # Single-cell trim_galore_args='--clip_R1 6 --clip_R2 6'
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Option to skip FastQ Screen.
--skip_fastq_screen
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Option to skip Trim Galore.
--skip_trim_galore
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Option to add extra arguments to FastQC.
--fastqc_args
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Option to add extra arguments to FastQ Screen.
--fastq_screen_args
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Option to add extra arguments to Trim Galore.
--trim_galore_args
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Option to add extra arguments to MultiQC.
--multiqc_args
This pipeline was adapted from the Nextflow pipelines created by the Babraham Institute Bioinformatics Group and from the nf-core pipelines. We thank all the contributors for both projects. We also thank the Nextflow community and the nf-core community for all the help and support.