Description Usage Arguments Value
This function takes a DATA.FRAME with TFBS positions, a BAM file with the sequence to analyze, a mean genome wide coverage, local coverage values for CNA, and outputs the corrected depth coverage values around TFBS and generates a TSS file with them. For better understanding check: https://www.nature.com/articles/s41467-019-12714-4
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 | calculate_coverage_tfbs(
bin_path = "tools/samtools/samtools",
ref_data = "",
bam = "",
sample_name = "",
tf_name = "",
mean_cov = "",
norm_log2 = "",
tfbs_start = 1000,
tfbs_end = 1000,
cov_limit = 1000,
mapq = 0,
threads = 1,
output_dir = ""
)
|
bin_path |
Path to binary. Default tools/samtools/samtools |
ref_data |
Data from BED file as Data.frame |
bam |
Path to BAM file. |
sample_name |
Sample name |
tf_name |
Transcription Factor name |
mean_cov |
Mean genome wide coverage. |
norm_log2 |
Data.frame with normalized local coverage |
tfbs_start |
Number of bases to analyze forward from TFBS central point. Default 1000 |
tfbs_end |
Number of bases to analyze backward from TFBS central point. Default 1000 |
cov_limit |
Max base depth. Default 1000 |
mapq |
Min quality of mapping reads. Default 0 |
threads |
Number of threads. Default 1 |
output_dir |
Directory to output results. If not provided then outputs in current directory |
max_regions |
Max number of TFBS to analyze. Default 100000 |
A list of DATA.FRAME with the coverage per base of each TFBS
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