View source: R/RegressHaplo_workflow.R
variant_calls_to_read_table.pipeline | R Documentation |
Given variant calls and a bam file, create a read table
variant_calls_to_read_table.pipeline( bam_file, out_dir, use_raw_read_table = F, sig = 0.01, debug = F )
bam_file |
path to bam file |
out_dir |
output directory, will be created if needed |
use_raw_read_table |
If there is an existing raw_read_table.csv file, should it be used as a raw read table? See details. |
sig |
significance levels at which to filter reads. |
Converts bam_file to a raw read table, written to $outdir/raw_read_table.csv and then applies error correction to reads and creates a filtered read table, written to $outdir/read_table.csv. The parameter use_raw_read_table can be used to skip the step of creating the raw read table, which is very time consuming. This is particularly useful, if the user wants to experiment with different error levels to form an acceptable read table.
path to read table file
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