Job ID = 5791694 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 5,992,738 reads read : 11,985,476 reads written : 5,992,738 reads 0-length : 5,992,738 rm: cannot remove ‘[DSE]RR*’: No such file or directory 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: 00:00:42 5992738 reads; of these: 5992738 (100.00%) were unpaired; of these: 338186 (5.64%) aligned 0 times 4745823 (79.19%) aligned exactly 1 time 908729 (15.16%) aligned >1 times 94.36% overall alignment rate Time searching: 00:00:42 Overall time: 00:00:42 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] 1552278 / 5654552 = 0.2745 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/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Wed, 22 Apr 2020 10:30:53: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.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 @ Wed, 22 Apr 2020 10:30:53: #1 read tag files... INFO @ Wed, 22 Apr 2020 10:30:53: #1 read treatment tags... INFO @ Wed, 22 Apr 2020 10:30:58: 1000000 INFO @ Wed, 22 Apr 2020 10:31:03: 2000000 INFO @ Wed, 22 Apr 2020 10:31:08: 3000000 INFO @ Wed, 22 Apr 2020 10:31:14: 4000000 INFO @ Wed, 22 Apr 2020 10:31:14: #1 tag size is determined as 51 bps INFO @ Wed, 22 Apr 2020 10:31:14: #1 tag size = 51 INFO @ Wed, 22 Apr 2020 10:31:14: #1 total tags in treatment: 4102274 INFO @ Wed, 22 Apr 2020 10:31:14: #1 user defined the maximum tags... INFO @ Wed, 22 Apr 2020 10:31:14: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Apr 2020 10:31:14: #1 tags after filtering in treatment: 4102274 INFO @ Wed, 22 Apr 2020 10:31:14: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 22 Apr 2020 10:31:14: #1 finished! INFO @ Wed, 22 Apr 2020 10:31:14: #2 Build Peak Model... INFO @ Wed, 22 Apr 2020 10:31:14: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Apr 2020 10:31:14: #2 number of paired peaks: 28 WARNING @ Wed, 22 Apr 2020 10:31:14: Too few paired peaks (28) 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 @ Wed, 22 Apr 2020 10:31:14: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.05_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/SRX7587254/SRX7587254.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Wed, 22 Apr 2020 10:31:21: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.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 @ Wed, 22 Apr 2020 10:31:21: #1 read tag files... INFO @ Wed, 22 Apr 2020 10:31:21: #1 read treatment tags... INFO @ Wed, 22 Apr 2020 10:31:25: 1000000 INFO @ Wed, 22 Apr 2020 10:31:30: 2000000 INFO @ Wed, 22 Apr 2020 10:31:34: 3000000 INFO @ Wed, 22 Apr 2020 10:31:39: 4000000 INFO @ Wed, 22 Apr 2020 10:31:39: #1 tag size is determined as 51 bps INFO @ Wed, 22 Apr 2020 10:31:39: #1 tag size = 51 INFO @ Wed, 22 Apr 2020 10:31:39: #1 total tags in treatment: 4102274 INFO @ Wed, 22 Apr 2020 10:31:39: #1 user defined the maximum tags... INFO @ Wed, 22 Apr 2020 10:31:39: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Apr 2020 10:31:39: #1 tags after filtering in treatment: 4102274 INFO @ Wed, 22 Apr 2020 10:31:39: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 22 Apr 2020 10:31:39: #1 finished! INFO @ Wed, 22 Apr 2020 10:31:39: #2 Build Peak Model... INFO @ Wed, 22 Apr 2020 10:31:39: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Apr 2020 10:31:39: #2 number of paired peaks: 28 WARNING @ Wed, 22 Apr 2020 10:31:39: Too few paired peaks (28) 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 @ Wed, 22 Apr 2020 10:31:39: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.10_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/SRX7587254/SRX7587254.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Wed, 22 Apr 2020 10:31:53: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.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 @ Wed, 22 Apr 2020 10:31:53: #1 read tag files... INFO @ Wed, 22 Apr 2020 10:31:53: #1 read treatment tags... INFO @ Wed, 22 Apr 2020 10:31:57: 1000000 INFO @ Wed, 22 Apr 2020 10:32:02: 2000000 INFO @ Wed, 22 Apr 2020 10:32:06: 3000000 INFO @ Wed, 22 Apr 2020 10:32:11: 4000000 INFO @ Wed, 22 Apr 2020 10:32:11: #1 tag size is determined as 51 bps INFO @ Wed, 22 Apr 2020 10:32:11: #1 tag size = 51 INFO @ Wed, 22 Apr 2020 10:32:11: #1 total tags in treatment: 4102274 INFO @ Wed, 22 Apr 2020 10:32:11: #1 user defined the maximum tags... INFO @ Wed, 22 Apr 2020 10:32:11: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Apr 2020 10:32:11: #1 tags after filtering in treatment: 4102274 INFO @ Wed, 22 Apr 2020 10:32:11: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 22 Apr 2020 10:32:11: #1 finished! INFO @ Wed, 22 Apr 2020 10:32:11: #2 Build Peak Model... INFO @ Wed, 22 Apr 2020 10:32:11: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Apr 2020 10:32:11: #2 number of paired peaks: 28 WARNING @ Wed, 22 Apr 2020 10:32:11: Too few paired peaks (28) 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 @ Wed, 22 Apr 2020 10:32:11: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.20_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7587254/SRX7587254.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。