Job ID = 14520719 SRX = SRX7119855 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 11192612 spots for SRR10423762/SRR10423762.sra Written 11192612 spots for SRR10423762/SRR10423762.sra fastq に変換しました。 bowtie でマッピング中... Time loading reference: 00:00:00 Time loading forward index: 00:00:00 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:02:28 11192612 reads; of these: 11192612 (100.00%) were unpaired; of these: 878860 (7.85%) aligned 0 times 9588592 (85.67%) aligned exactly 1 time 725160 (6.48%) aligned >1 times 92.15% overall alignment rate Time searching: 00:02:28 Overall time: 00:02:28 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 17 sequences. [bam_sort_core] merging from 8 files... [bam_rmdupse_core] 3545578 / 10313752 = 0.3438 in library ' ' BAM に変換しました。 Bed ファイルを作成中... WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 19:48:01: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.bam'] # control file = None # effective genome size = 1.21e+07 # band width = 300 # model fold = [5, 50] # qvalue cutoff = 1.00e-05 # Larger dataset will be scaled towards smaller dataset. # Range for calculating regional lambda is: 10000 bps # Broad region calling is off # Paired-End mode is off INFO @ Sat, 15 Jan 2022 19:48:01: #1 read tag files... INFO @ Sat, 15 Jan 2022 19:48:01: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 19:48:07: 1000000 INFO @ Sat, 15 Jan 2022 19:48:14: 2000000 INFO @ Sat, 15 Jan 2022 19:48:20: 3000000 INFO @ Sat, 15 Jan 2022 19:48:27: 4000000 WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 19:48:31: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.bam'] # control file = None # effective genome size = 1.21e+07 # band width = 300 # model fold = [5, 50] # qvalue cutoff = 1.00e-10 # Larger dataset will be scaled towards smaller dataset. # Range for calculating regional lambda is: 10000 bps # Broad region calling is off # Paired-End mode is off INFO @ Sat, 15 Jan 2022 19:48:31: #1 read tag files... INFO @ Sat, 15 Jan 2022 19:48:31: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 19:48:33: 5000000 INFO @ Sat, 15 Jan 2022 19:48:38: 1000000 INFO @ Sat, 15 Jan 2022 19:48:40: 6000000 INFO @ Sat, 15 Jan 2022 19:48:46: 2000000 INFO @ Sat, 15 Jan 2022 19:48:46: #1 tag size is determined as 101 bps INFO @ Sat, 15 Jan 2022 19:48:46: #1 tag size = 101 INFO @ Sat, 15 Jan 2022 19:48:46: #1 total tags in treatment: 6768174 INFO @ Sat, 15 Jan 2022 19:48:46: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 19:48:46: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 19:48:46: #1 tags after filtering in treatment: 6768174 INFO @ Sat, 15 Jan 2022 19:48:46: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 19:48:46: #1 finished! INFO @ Sat, 15 Jan 2022 19:48:46: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 19:48:46: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 19:48:46: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 19:48:46: Too few paired peaks (0) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead. WARNING @ Sat, 15 Jan 2022 19:48:46: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.05_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 0 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 19:48:53: 3000000 BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 19:49:00: 4000000 INFO @ Sat, 15 Jan 2022 19:49:01: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.bam'] # control file = None # effective genome size = 1.21e+07 # band width = 300 # model fold = [5, 50] # qvalue cutoff = 1.00e-20 # Larger dataset will be scaled towards smaller dataset. # Range for calculating regional lambda is: 10000 bps # Broad region calling is off # Paired-End mode is off INFO @ Sat, 15 Jan 2022 19:49:01: #1 read tag files... INFO @ Sat, 15 Jan 2022 19:49:01: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 19:49:07: 5000000 INFO @ Sat, 15 Jan 2022 19:49:08: 1000000 INFO @ Sat, 15 Jan 2022 19:49:15: 6000000 INFO @ Sat, 15 Jan 2022 19:49:16: 2000000 INFO @ Sat, 15 Jan 2022 19:49:20: #1 tag size is determined as 101 bps INFO @ Sat, 15 Jan 2022 19:49:20: #1 tag size = 101 INFO @ Sat, 15 Jan 2022 19:49:20: #1 total tags in treatment: 6768174 INFO @ Sat, 15 Jan 2022 19:49:20: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 19:49:20: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 19:49:20: #1 tags after filtering in treatment: 6768174 INFO @ Sat, 15 Jan 2022 19:49:20: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 19:49:20: #1 finished! INFO @ Sat, 15 Jan 2022 19:49:20: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 19:49:20: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 19:49:21: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 19:49:21: Too few paired peaks (0) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead. WARNING @ Sat, 15 Jan 2022 19:49:21: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.10_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 19:49:23: 3000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 19:49:30: 4000000 BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 19:49:36: 5000000 INFO @ Sat, 15 Jan 2022 19:49:42: 6000000 INFO @ Sat, 15 Jan 2022 19:49:47: #1 tag size is determined as 101 bps INFO @ Sat, 15 Jan 2022 19:49:47: #1 tag size = 101 INFO @ Sat, 15 Jan 2022 19:49:47: #1 total tags in treatment: 6768174 INFO @ Sat, 15 Jan 2022 19:49:47: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 19:49:47: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 19:49:47: #1 tags after filtering in treatment: 6768174 INFO @ Sat, 15 Jan 2022 19:49:47: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 19:49:47: #1 finished! INFO @ Sat, 15 Jan 2022 19:49:47: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 19:49:47: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 19:49:48: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 19:49:48: Too few paired peaks (0) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead. WARNING @ Sat, 15 Jan 2022 19:49:48: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.20_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7119855/SRX7119855.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling