View source: R/setting_handler.R
set_settings | R Documentation |
Set Settings.
set_settings( SCAR_obj, analysis_type = NA, paired = NA, ncores = NA, genome_dir = NA, genome_index = NA, genome_assembly = NA, alignment_dir = NA, peak_dir = NA, compare = NA, plot_dir = NA, comp_op = NA )
SCAR_obj |
SCAR object, holds data for use in all the functions. |
analysis_type |
Type of experiment. 'ChIP-seq', 'ChEC-seq', or 'SChEC-seq'. |
paired |
Paired-end status of the reads. Either TRUE or FALSE. |
ncores |
The number of cores/threads to use. |
genome_dir |
The directory of the genome index. |
genome_index |
The location of the bowtie2 genome index |
genome_assembly |
The directory and file name of the the gnome assembly FASTA file. |
alignment_dir |
The directory containing the aligned reads. |
peak_dir |
The directory containing the called peaks. |
compare |
For deeptools, do you want to use bamCompare? |
plot_dir |
directory for plotting outputs |
comp_op |
Single operation for comparison of coverage |
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