Align from FASTQ, generate sorted and indexed BAM file
Source:R/refgenome.R
BascetAlignToReference.RdAlign from FASTQ, generate sorted and indexed BAM file
Usage
BascetAlignToReference(
bascetRoot,
useReference,
numThreads = NULL,
totalMem = NULL,
inputName = "filtered",
outputNameBAMcell = "aligned_cell",
outputNameBAMpos = "aligned_pos",
overwrite = FALSE,
aligner = c(NULL, "BWA", "bowtie2", "STAR"),
runner = GetDefaultBascetRunner(),
bascetInstance = GetDefaultBascetInstance()
)Arguments
- bascetRoot
The root folder where all Bascets are stored
- useReference
Name of the BWA reference to use
- numThreads
Number of threads to use for each runner. Default is the maximum, taken from runner settings
- totalMem
Total memory to allocate
- inputName
Name of input shard
- outputNameBAMcell
Name of cell-sorted BAMs
- outputNameBAMpos
Name of pos-sorted BAMs (if generated)
- overwrite
Force overwriting of existing files. The default is to do nothing files exist
- aligner
Which aligner to use: "BWA", "bowtie2", or "STAR"
- runner
The job manager, specifying how the command will be run (e.g. locally, or via SLURM)
- bascetInstance
A Bascet instance