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 |
- |