Job ID = 14520753 SRX = SRX9431314 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 7558225 spots for SRR12979607/SRR12979607.sra Written 7558225 spots for SRR12979607/SRR12979607.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: 00:01:18 7558225 reads; of these: 7558225 (100.00%) were unpaired; of these: 684755 (9.06%) aligned 0 times 5996646 (79.34%) aligned exactly 1 time 876824 (11.60%) aligned >1 times 90.94% overall alignment rate Time searching: 00:01:18 Overall time: 00:01:18 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_rmdupse_core] 1910387 / 6873470 = 0.2779 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 19:50:47: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.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 19:50:47: #1 read tag files... INFO @ Sat, 15 Jan 2022 19:50:47: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 19:50:52: 1000000 INFO @ Sat, 15 Jan 2022 19:50:58: 2000000 INFO @ Sat, 15 Jan 2022 19:51:03: 3000000 INFO @ Sat, 15 Jan 2022 19:51:09: 4000000 INFO @ Sat, 15 Jan 2022 19:51:14: #1 tag size is determined as 66 bps INFO @ Sat, 15 Jan 2022 19:51:14: #1 tag size = 66 INFO @ Sat, 15 Jan 2022 19:51:14: #1 total tags in treatment: 4963083 INFO @ Sat, 15 Jan 2022 19:51:14: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 19:51:14: #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 19:51:14: #1 tags after filtering in treatment: 4963083 INFO @ Sat, 15 Jan 2022 19:51:14: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 19:51:14: #1 finished! INFO @ Sat, 15 Jan 2022 19:51:14: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 19:51:14: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 19:51:14: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 19:51:14: 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 19:51:14: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.05_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/SRX9431314/SRX9431314.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling 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 19:51:17: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.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 19:51:17: #1 read tag files... INFO @ Sat, 15 Jan 2022 19:51:17: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 19:51:21: 1000000 INFO @ Sat, 15 Jan 2022 19:51:26: 2000000 INFO @ Sat, 15 Jan 2022 19:51:30: 3000000 INFO @ Sat, 15 Jan 2022 19:51:35: 4000000 INFO @ Sat, 15 Jan 2022 19:51:40: #1 tag size is determined as 66 bps INFO @ Sat, 15 Jan 2022 19:51:40: #1 tag size = 66 INFO @ Sat, 15 Jan 2022 19:51:40: #1 total tags in treatment: 4963083 INFO @ Sat, 15 Jan 2022 19:51:40: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 19:51:40: #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 19:51:40: #1 tags after filtering in treatment: 4963083 INFO @ Sat, 15 Jan 2022 19:51:40: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 19:51:40: #1 finished! INFO @ Sat, 15 Jan 2022 19:51:40: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 19:51:40: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 19:51:40: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 19:51:40: 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 19:51:40: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.10_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/SRX9431314/SRX9431314.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling 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 19:51:47: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.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 19:51:47: #1 read tag files... INFO @ Sat, 15 Jan 2022 19:51:47: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 19:51:52: 1000000 INFO @ Sat, 15 Jan 2022 19:51:58: 2000000 INFO @ Sat, 15 Jan 2022 19:52:03: 3000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 19:52:09: 4000000 BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 19:52:14: #1 tag size is determined as 66 bps INFO @ Sat, 15 Jan 2022 19:52:14: #1 tag size = 66 INFO @ Sat, 15 Jan 2022 19:52:14: #1 total tags in treatment: 4963083 INFO @ Sat, 15 Jan 2022 19:52:14: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 19:52:14: #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 19:52:14: #1 tags after filtering in treatment: 4963083 INFO @ Sat, 15 Jan 2022 19:52:14: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 19:52:14: #1 finished! INFO @ Sat, 15 Jan 2022 19:52:14: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 19:52:14: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 19:52:14: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 19:52:14: 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 19:52:14: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.20_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/SRX9431314/SRX9431314.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9431314/SRX9431314.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling