
Inactive Modules:
  1) slurm

INFO  @ Mon, 24 Feb 2025 15:08:21: 
# Command line: callpeak -t T1P_HA_hg38_sorted.bam -c T1P_IgG_hg38_sorted.bam -f BAM -g hs -n T1P_HA_hg38_callpeaks1 --call-summits -q 0.05 --bdg
# ARGUMENTS LIST:
# name = T1P_HA_hg38_callpeaks1
# format = BAM
# ChIP-seq file = ['T1P_HA_hg38_sorted.bam']
# control file = ['T1P_IgG_hg38_sorted.bam']
# effective genome size = 2.70e+09
# band width = 300
# model fold = [5, 50]
# qvalue cutoff = 5.00e-02
# The maximum gap between significant sites is assigned as the read length/tag size.
# The minimum length of peaks is assigned as the predicted fragment length "d".
# Larger dataset will be scaled towards smaller dataset.
# Range for calculating regional lambda is: 1000 bps and 10000 bps
# Broad region calling is off
# Paired-End mode is off
# Searching for subpeak summits is on
 
INFO  @ Mon, 24 Feb 2025 15:08:21: #1 read tag files... 
INFO  @ Mon, 24 Feb 2025 15:08:21: #1 read treatment tags... 
INFO  @ Mon, 24 Feb 2025 15:08:27:  1000000 
INFO  @ Mon, 24 Feb 2025 15:08:32:  2000000 
INFO  @ Mon, 24 Feb 2025 15:08:46: 2880259 reads have been read. 
INFO  @ Mon, 24 Feb 2025 15:08:46: #1.2 read input tags... 
INFO  @ Mon, 24 Feb 2025 15:08:52:  1000000 
INFO  @ Mon, 24 Feb 2025 15:08:57:  2000000 
INFO  @ Mon, 24 Feb 2025 15:09:03:  3000000 
INFO  @ Mon, 24 Feb 2025 15:09:09:  4000000 
INFO  @ Mon, 24 Feb 2025 15:09:14:  5000000 
INFO  @ Mon, 24 Feb 2025 15:09:20:  6000000 
INFO  @ Mon, 24 Feb 2025 15:09:40: 6890662 reads have been read. 
INFO  @ Mon, 24 Feb 2025 15:09:40: #1 tag size is determined as 101 bps 
INFO  @ Mon, 24 Feb 2025 15:09:40: #1 tag size = 101.0 
INFO  @ Mon, 24 Feb 2025 15:09:40: #1  total tags in treatment: 2880259 
INFO  @ Mon, 24 Feb 2025 15:09:40: #1 user defined the maximum tags... 
INFO  @ Mon, 24 Feb 2025 15:09:40: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) 
INFO  @ Mon, 24 Feb 2025 15:09:40: #1  tags after filtering in treatment: 2807962 
INFO  @ Mon, 24 Feb 2025 15:09:40: #1  Redundant rate of treatment: 0.03 
INFO  @ Mon, 24 Feb 2025 15:09:40: #1  total tags in control: 6890662 
INFO  @ Mon, 24 Feb 2025 15:09:40: #1 user defined the maximum tags... 
INFO  @ Mon, 24 Feb 2025 15:09:40: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) 
INFO  @ Mon, 24 Feb 2025 15:09:40: #1  tags after filtering in control: 6700819 
INFO  @ Mon, 24 Feb 2025 15:09:40: #1  Redundant rate of control: 0.03 
INFO  @ Mon, 24 Feb 2025 15:09:40: #1 finished! 
INFO  @ Mon, 24 Feb 2025 15:09:40: #2 Build Peak Model... 
INFO  @ Mon, 24 Feb 2025 15:09:40: #2 looking for paired plus/minus strand peaks... 
INFO  @ Mon, 24 Feb 2025 15:09:43: #2 number of paired peaks: 19958 
INFO  @ Mon, 24 Feb 2025 15:09:43: start model_add_line... 
INFO  @ Mon, 24 Feb 2025 15:09:43: start X-correlation... 
INFO  @ Mon, 24 Feb 2025 15:09:43: end of X-cor 
INFO  @ Mon, 24 Feb 2025 15:09:43: #2 finished! 
INFO  @ Mon, 24 Feb 2025 15:09:43: #2 predicted fragment length is 296 bps 
INFO  @ Mon, 24 Feb 2025 15:09:43: #2 alternative fragment length(s) may be 296 bps 
INFO  @ Mon, 24 Feb 2025 15:09:43: #2.2 Generate R script for model : T1P_HA_hg38_callpeaks1_model.r 
INFO  @ Mon, 24 Feb 2025 15:09:43: #3 Call peaks... 
INFO  @ Mon, 24 Feb 2025 15:09:43: #3 Going to call summits inside each peak ... 
INFO  @ Mon, 24 Feb 2025 15:09:43: #3 Pre-compute pvalue-qvalue table... 
INFO  @ Mon, 24 Feb 2025 15:10:11: #3 In the peak calling step, the following will be performed simultaneously: 
INFO  @ Mon, 24 Feb 2025 15:10:11: #3   Write bedGraph files for treatment pileup (after scaling if necessary)... T1P_HA_hg38_callpeaks1_treat_pileup.bdg 
INFO  @ Mon, 24 Feb 2025 15:10:11: #3   Write bedGraph files for control lambda (after scaling if necessary)... T1P_HA_hg38_callpeaks1_control_lambda.bdg 
INFO  @ Mon, 24 Feb 2025 15:10:11: #3   Pileup will be based on sequencing depth in treatment. 
INFO  @ Mon, 24 Feb 2025 15:10:11: #3 Call peaks for each chromosome... 
INFO  @ Mon, 24 Feb 2025 15:10:39: #4 Write output xls file... T1P_HA_hg38_callpeaks1_peaks.xls 
INFO  @ Mon, 24 Feb 2025 15:10:39: #4 Write peak in narrowPeak format file... T1P_HA_hg38_callpeaks1_peaks.narrowPeak 
INFO  @ Mon, 24 Feb 2025 15:10:39: #4 Write summits bed file... T1P_HA_hg38_callpeaks1_summits.bed 
INFO  @ Mon, 24 Feb 2025 15:10:39: Done! 
INFO  @ Mon, 24 Feb 2025 15:10:39: 
# Command line: callpeak -t T2P_HA_hg38_sorted.bam -c T2P_IgG_hg38_sorted.bam -f BAM -g hs -n T2P_HA_hg38_callpeaks1 --call-summits -q 0.05 --bdg
# ARGUMENTS LIST:
# name = T2P_HA_hg38_callpeaks1
# format = BAM
# ChIP-seq file = ['T2P_HA_hg38_sorted.bam']
# control file = ['T2P_IgG_hg38_sorted.bam']
# effective genome size = 2.70e+09
# band width = 300
# model fold = [5, 50]
# qvalue cutoff = 5.00e-02
# The maximum gap between significant sites is assigned as the read length/tag size.
# The minimum length of peaks is assigned as the predicted fragment length "d".
# Larger dataset will be scaled towards smaller dataset.
# Range for calculating regional lambda is: 1000 bps and 10000 bps
# Broad region calling is off
# Paired-End mode is off
# Searching for subpeak summits is on
 
INFO  @ Mon, 24 Feb 2025 15:10:39: #1 read tag files... 
INFO  @ Mon, 24 Feb 2025 15:10:39: #1 read treatment tags... 
INFO  @ Mon, 24 Feb 2025 15:10:45:  1000000 
INFO  @ Mon, 24 Feb 2025 15:10:51:  2000000 
INFO  @ Mon, 24 Feb 2025 15:10:56:  3000000 
INFO  @ Mon, 24 Feb 2025 15:11:03: 3213360 reads have been read. 
INFO  @ Mon, 24 Feb 2025 15:11:03: #1.2 read input tags... 
INFO  @ Mon, 24 Feb 2025 15:11:08:  1000000 
INFO  @ Mon, 24 Feb 2025 15:11:14:  2000000 
INFO  @ Mon, 24 Feb 2025 15:11:19:  3000000 
INFO  @ Mon, 24 Feb 2025 15:11:24:  4000000 
INFO  @ Mon, 24 Feb 2025 15:11:30:  5000000 
INFO  @ Mon, 24 Feb 2025 15:11:42: 5061712 reads have been read. 
INFO  @ Mon, 24 Feb 2025 15:11:42: #1 tag size is determined as 101 bps 
INFO  @ Mon, 24 Feb 2025 15:11:42: #1 tag size = 101.0 
INFO  @ Mon, 24 Feb 2025 15:11:42: #1  total tags in treatment: 3213360 
INFO  @ Mon, 24 Feb 2025 15:11:42: #1 user defined the maximum tags... 
INFO  @ Mon, 24 Feb 2025 15:11:42: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) 
INFO  @ Mon, 24 Feb 2025 15:11:42: #1  tags after filtering in treatment: 3134266 
INFO  @ Mon, 24 Feb 2025 15:11:42: #1  Redundant rate of treatment: 0.02 
INFO  @ Mon, 24 Feb 2025 15:11:42: #1  total tags in control: 5061712 
INFO  @ Mon, 24 Feb 2025 15:11:42: #1 user defined the maximum tags... 
INFO  @ Mon, 24 Feb 2025 15:11:42: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) 
INFO  @ Mon, 24 Feb 2025 15:11:42: #1  tags after filtering in control: 4929779 
INFO  @ Mon, 24 Feb 2025 15:11:42: #1  Redundant rate of control: 0.03 
INFO  @ Mon, 24 Feb 2025 15:11:42: #1 finished! 
INFO  @ Mon, 24 Feb 2025 15:11:42: #2 Build Peak Model... 
INFO  @ Mon, 24 Feb 2025 15:11:42: #2 looking for paired plus/minus strand peaks... 
INFO  @ Mon, 24 Feb 2025 15:11:46: #2 number of paired peaks: 29997 
INFO  @ Mon, 24 Feb 2025 15:11:46: start model_add_line... 
INFO  @ Mon, 24 Feb 2025 15:11:46: start X-correlation... 
INFO  @ Mon, 24 Feb 2025 15:11:46: end of X-cor 
INFO  @ Mon, 24 Feb 2025 15:11:46: #2 finished! 
INFO  @ Mon, 24 Feb 2025 15:11:46: #2 predicted fragment length is 297 bps 
INFO  @ Mon, 24 Feb 2025 15:11:46: #2 alternative fragment length(s) may be 297 bps 
INFO  @ Mon, 24 Feb 2025 15:11:46: #2.2 Generate R script for model : T2P_HA_hg38_callpeaks1_model.r 
INFO  @ Mon, 24 Feb 2025 15:11:46: #3 Call peaks... 
INFO  @ Mon, 24 Feb 2025 15:11:46: #3 Going to call summits inside each peak ... 
INFO  @ Mon, 24 Feb 2025 15:11:46: #3 Pre-compute pvalue-qvalue table... 
INFO  @ Mon, 24 Feb 2025 15:12:06: #3 In the peak calling step, the following will be performed simultaneously: 
INFO  @ Mon, 24 Feb 2025 15:12:06: #3   Write bedGraph files for treatment pileup (after scaling if necessary)... T2P_HA_hg38_callpeaks1_treat_pileup.bdg 
INFO  @ Mon, 24 Feb 2025 15:12:06: #3   Write bedGraph files for control lambda (after scaling if necessary)... T2P_HA_hg38_callpeaks1_control_lambda.bdg 
INFO  @ Mon, 24 Feb 2025 15:12:06: #3   Pileup will be based on sequencing depth in treatment. 
INFO  @ Mon, 24 Feb 2025 15:12:06: #3 Call peaks for each chromosome... 
INFO  @ Mon, 24 Feb 2025 15:12:27: #4 Write output xls file... T2P_HA_hg38_callpeaks1_peaks.xls 
INFO  @ Mon, 24 Feb 2025 15:12:27: #4 Write peak in narrowPeak format file... T2P_HA_hg38_callpeaks1_peaks.narrowPeak 
INFO  @ Mon, 24 Feb 2025 15:12:27: #4 Write summits bed file... T2P_HA_hg38_callpeaks1_summits.bed 
INFO  @ Mon, 24 Feb 2025 15:12:27: Done! 
