Job ID = 14168371 SRX = SRX8688894 Genome = dm3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 5797613 spots for SRR12174205/SRR12174205.sra Written 5797613 spots for SRR12174205/SRR12174205.sra fastq に変換しました。 bowtie でマッピング中... Your job 14169536 ("srTdm6") has been submitted Time loading reference: 00:00:00 Time loading forward index: 00:00:00 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:01:31 5797613 reads; of these: 5797613 (100.00%) were unpaired; of these: 468116 (8.07%) aligned 0 times 4536396 (78.25%) aligned exactly 1 time 793101 (13.68%) aligned >1 times 91.93% overall alignment rate Time searching: 00:01:31 Overall time: 00:01:31 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 15 sequences. [bam_rmdupse_core] 196829 / 5329497 = 0.0369 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 @ Fri, 10 Dec 2021 18:15:33: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Fri, 10 Dec 2021 18:15:33: #1 read tag files... INFO @ Fri, 10 Dec 2021 18:15:33: #1 read treatment tags... INFO @ Fri, 10 Dec 2021 18:15:39: 1000000 INFO @ Fri, 10 Dec 2021 18:15:44: 2000000 INFO @ Fri, 10 Dec 2021 18:15:49: 3000000 INFO @ Fri, 10 Dec 2021 18:15:55: 4000000 INFO @ Fri, 10 Dec 2021 18:16:00: 5000000 INFO @ Fri, 10 Dec 2021 18:16:01: #1 tag size is determined as 50 bps INFO @ Fri, 10 Dec 2021 18:16:01: #1 tag size = 50 INFO @ Fri, 10 Dec 2021 18:16:01: #1 total tags in treatment: 5132668 INFO @ Fri, 10 Dec 2021 18:16:01: #1 user defined the maximum tags... INFO @ Fri, 10 Dec 2021 18:16:01: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Dec 2021 18:16:01: #1 tags after filtering in treatment: 5132668 INFO @ Fri, 10 Dec 2021 18:16:01: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 10 Dec 2021 18:16:01: #1 finished! INFO @ Fri, 10 Dec 2021 18:16:01: #2 Build Peak Model... INFO @ Fri, 10 Dec 2021 18:16:01: #2 looking for paired plus/minus strand peaks... 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 @ Fri, 10 Dec 2021 18:16:01: #2 number of paired peaks: 25 WARNING @ Fri, 10 Dec 2021 18:16:01: Too few paired peaks (25) 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 @ Fri, 10 Dec 2021 18:16:01: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.05_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/dm3/SRX8688894/SRX8688894.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 10 Dec 2021 18:16:03: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Fri, 10 Dec 2021 18:16:03: #1 read tag files... INFO @ Fri, 10 Dec 2021 18:16:03: #1 read treatment tags... INFO @ Fri, 10 Dec 2021 18:16:08: 1000000 INFO @ Fri, 10 Dec 2021 18:16:14: 2000000 INFO @ Fri, 10 Dec 2021 18:16:19: 3000000 INFO @ Fri, 10 Dec 2021 18:16:24: 4000000 INFO @ Fri, 10 Dec 2021 18:16:29: 5000000 INFO @ Fri, 10 Dec 2021 18:16:30: #1 tag size is determined as 50 bps INFO @ Fri, 10 Dec 2021 18:16:30: #1 tag size = 50 INFO @ Fri, 10 Dec 2021 18:16:30: #1 total tags in treatment: 5132668 INFO @ Fri, 10 Dec 2021 18:16:30: #1 user defined the maximum tags... INFO @ Fri, 10 Dec 2021 18:16:30: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Dec 2021 18:16:30: #1 tags after filtering in treatment: 5132668 INFO @ Fri, 10 Dec 2021 18:16:30: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 10 Dec 2021 18:16:30: #1 finished! INFO @ Fri, 10 Dec 2021 18:16:30: #2 Build Peak Model... INFO @ Fri, 10 Dec 2021 18:16:30: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Dec 2021 18:16:30: #2 number of paired peaks: 25 WARNING @ Fri, 10 Dec 2021 18:16:30: Too few paired peaks (25) 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 @ Fri, 10 Dec 2021 18:16:30: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.10_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/dm3/SRX8688894/SRX8688894.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.10_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 @ Fri, 10 Dec 2021 18:16:33: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Fri, 10 Dec 2021 18:16:33: #1 read tag files... INFO @ Fri, 10 Dec 2021 18:16:33: #1 read treatment tags... INFO @ Fri, 10 Dec 2021 18:16:39: 1000000 INFO @ Fri, 10 Dec 2021 18:16:45: 2000000 INFO @ Fri, 10 Dec 2021 18:16:51: 3000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Fri, 10 Dec 2021 18:16:56: 4000000 INFO @ Fri, 10 Dec 2021 18:17:02: 5000000 INFO @ Fri, 10 Dec 2021 18:17:03: #1 tag size is determined as 50 bps INFO @ Fri, 10 Dec 2021 18:17:03: #1 tag size = 50 INFO @ Fri, 10 Dec 2021 18:17:03: #1 total tags in treatment: 5132668 INFO @ Fri, 10 Dec 2021 18:17:03: #1 user defined the maximum tags... INFO @ Fri, 10 Dec 2021 18:17:03: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Dec 2021 18:17:03: #1 tags after filtering in treatment: 5132668 INFO @ Fri, 10 Dec 2021 18:17:03: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 10 Dec 2021 18:17:03: #1 finished! INFO @ Fri, 10 Dec 2021 18:17:03: #2 Build Peak Model... INFO @ Fri, 10 Dec 2021 18:17:03: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Dec 2021 18:17:03: #2 number of paired peaks: 25 WARNING @ Fri, 10 Dec 2021 18:17:03: Too few paired peaks (25) 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 @ Fri, 10 Dec 2021 18:17:03: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.20_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/dm3/SRX8688894/SRX8688894.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8688894/SRX8688894.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BigWig に変換しました。