new_index_bam_samtools | R Documentation |
This function sorts a genome sequence file (BAM/SAM)
new_index_bam_samtools(
bin_samtools = build_default_tool_binary_list()$bin_samtools,
bam = NULL,
stats = TRUE,
...
)
bam |
Path to the input file with the sequence. |
bin_samtols |
Path to samtools executable. Default path tools/samtools/samtools. |
verbose |
Enables progress messages. Default False. |
threads |
Number of threads. Default 3 |
ram |
Ram memory to use per thread in GB. Default 1GB |
output_dir |
Path to the output directory. |
coord_sort |
Generate a coord sorted file. Otherwise queryname sorted. Default TRUE |
clean |
Remove input files. Default FALSE |
mode |
REQUIRED Where to parallelize. Default local. Options "local","batch" |
executor_id |
Task EXECUTOR ID. Default "mardupsGATK" |
task_name |
Name of the task. Default "mardupsGATK" |
time |
OPTIONAL If batch mode. Max run time per job. Default "48:0:0" |
update_time |
OPTIONAL If batch mode. Job update time in seconds. Default 60. |
wait |
OPTIONAL If batch mode wait for batch to finish. Default FALSE |
hold |
OPTIONAL Hold job until job is finished. Job ID. |
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