Job ID = 14520325 SRX = SRX11361078 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 22763097 spots for SRR15050655/SRR15050655.sra Written 22763097 spots for SRR15050655/SRR15050655.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: 00:03:55 22763097 reads; of these: 22763097 (100.00%) were unpaired; of these: 3151341 (13.84%) aligned 0 times 13694447 (60.16%) aligned exactly 1 time 5917309 (26.00%) aligned >1 times 86.16% overall alignment rate Time searching: 00:03:55 Overall time: 00:03:55 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] 14500669 / 19611756 = 0.7394 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 19:06:09: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.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 19:06:09: #1 read tag files... INFO @ Sat, 15 Jan 2022 19:06:09: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 19:06:14: 1000000 INFO @ Sat, 15 Jan 2022 19:06:20: 2000000 INFO @ Sat, 15 Jan 2022 19:06:26: 3000000 INFO @ Sat, 15 Jan 2022 19:06:32: 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 19:06:38: 5000000 INFO @ Sat, 15 Jan 2022 19:06:39: #1 tag size is determined as 67 bps INFO @ Sat, 15 Jan 2022 19:06:39: #1 tag size = 67 INFO @ Sat, 15 Jan 2022 19:06:39: #1 total tags in treatment: 5111087 INFO @ Sat, 15 Jan 2022 19:06:39: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 19:06:39: #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 19:06:39: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.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 19:06:39: #1 read tag files... INFO @ Sat, 15 Jan 2022 19:06:39: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 19:06:39: #1 tags after filtering in treatment: 5111087 INFO @ Sat, 15 Jan 2022 19:06:39: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 19:06:39: #1 finished! INFO @ Sat, 15 Jan 2022 19:06:39: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 19:06:39: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 19:06:39: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 19:06:39: 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 19:06:39: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.05_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/SRX11361078/SRX11361078.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 19:06:44: 1000000 INFO @ Sat, 15 Jan 2022 19:06:49: 2000000 INFO @ Sat, 15 Jan 2022 19:06:54: 3000000 INFO @ Sat, 15 Jan 2022 19:06:59: 4000000 INFO @ Sat, 15 Jan 2022 19:07:04: 5000000 INFO @ Sat, 15 Jan 2022 19:07:05: #1 tag size is determined as 67 bps INFO @ Sat, 15 Jan 2022 19:07:05: #1 tag size = 67 INFO @ Sat, 15 Jan 2022 19:07:05: #1 total tags in treatment: 5111087 INFO @ Sat, 15 Jan 2022 19:07:05: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 19:07:05: #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 19:07:05: #1 tags after filtering in treatment: 5111087 INFO @ Sat, 15 Jan 2022 19:07:05: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 19:07:05: #1 finished! INFO @ Sat, 15 Jan 2022 19:07:05: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 19:07:05: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 19:07:05: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 19:07:05: 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 19:07:05: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.10_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/SRX11361078/SRX11361078.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.10_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 19:07:09: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.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 19:07:09: #1 read tag files... INFO @ Sat, 15 Jan 2022 19:07:09: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 19:07:14: 1000000 INFO @ Sat, 15 Jan 2022 19:07:19: 2000000 INFO @ Sat, 15 Jan 2022 19:07:24: 3000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 19:07:29: 4000000 INFO @ Sat, 15 Jan 2022 19:07:34: 5000000 INFO @ Sat, 15 Jan 2022 19:07:35: #1 tag size is determined as 67 bps INFO @ Sat, 15 Jan 2022 19:07:35: #1 tag size = 67 INFO @ Sat, 15 Jan 2022 19:07:35: #1 total tags in treatment: 5111087 INFO @ Sat, 15 Jan 2022 19:07:35: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 19:07:35: #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 19:07:35: #1 tags after filtering in treatment: 5111087 INFO @ Sat, 15 Jan 2022 19:07:35: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 19:07:35: #1 finished! INFO @ Sat, 15 Jan 2022 19:07:35: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 19:07:35: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 19:07:35: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 19:07:35: 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 19:07:35: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.20_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/SRX11361078/SRX11361078.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX11361078/SRX11361078.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BigWig に変換しました。