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. Author manuscript; available in PMC: 2019 Apr 15.
Published in final edited form as: Methods Enzymol. 2018 Feb 26;601:391–418. doi: 10.1016/bs.mie.2017.11.037
Argument Synopsis (* = required) Detail
Note: either --bam OR --fq1 & --fq2 arguments are required
--bam *Input BAM file Full path to a paired-end BAM file
--fq1 *Input fastq for read 1 Full path to a fastq / fastq.gz file for read 1
--fq2 *Input fastq for read 2 Full path to a fastq / fastq.gz file for read 2
--g *Genome name Name must match a folder in $SSDSGENOMESPATH
--n Number of threads (for alignment step) Default = 12
--r1BP Trim size for read 1 (bp) Integer value (default = 36)
--r2BP Trim size for read 2 (bp) Integer value (default = 40)
--splitSz Large BAM files are split for ssDNA detection. A lower value reduces the memory footprint (default = 20000000)
--outdir Output folder Defaults to BAM / FASTQ folder
--sample Sample name for read group -
--date Date for read group Date in DDMMYY format
--lane Lane for read group -
--bwaVers Bwa version to use 0.5 or 0.7 [default]
--v Use verbose mode -
--h/help Show help -