Job ID = 14170487 SRX = SRX8689048 Genome = dm3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 5752649 spots for SRR12174191/SRR12174191.sra Written 5752649 spots for SRR12174191/SRR12174191.sra fastq に変換しました。 bowtie でマッピング中... Your job 14170887 ("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: 00:01:26 5752649 reads; of these: 5752649 (100.00%) were unpaired; of these: 672339 (11.69%) aligned 0 times 4370069 (75.97%) aligned exactly 1 time 710241 (12.35%) aligned >1 times 88.31% overall alignment rate Time searching: 00:01:26 Overall time: 00:01:26 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] 134750 / 5080310 = 0.0265 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, 11 Dec 2021 06:59:23: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.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 @ Sat, 11 Dec 2021 06:59:23: #1 read tag files... INFO @ Sat, 11 Dec 2021 06:59:23: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 06:59:28: 1000000 INFO @ Sat, 11 Dec 2021 06:59:33: 2000000 INFO @ Sat, 11 Dec 2021 06:59:39: 3000000 INFO @ Sat, 11 Dec 2021 06:59:44: 4000000 INFO @ Sat, 11 Dec 2021 06:59:49: #1 tag size is determined as 50 bps INFO @ Sat, 11 Dec 2021 06:59:49: #1 tag size = 50 INFO @ Sat, 11 Dec 2021 06:59:49: #1 total tags in treatment: 4945560 INFO @ Sat, 11 Dec 2021 06:59:49: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 06:59:49: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 11 Dec 2021 06:59:49: #1 tags after filtering in treatment: 4945560 INFO @ Sat, 11 Dec 2021 06:59:49: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 11 Dec 2021 06:59:49: #1 finished! INFO @ Sat, 11 Dec 2021 06:59:49: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 06:59:49: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 06:59:49: #2 number of paired peaks: 49 WARNING @ Sat, 11 Dec 2021 06:59:49: Too few paired peaks (49) 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, 11 Dec 2021 06:59:49: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.05_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/dm3/SRX8689048/SRX8689048.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.05_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, 11 Dec 2021 06:59:53: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.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 @ Sat, 11 Dec 2021 06:59:53: #1 read tag files... INFO @ Sat, 11 Dec 2021 06:59:53: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 06:59:59: 1000000 INFO @ Sat, 11 Dec 2021 07:00:05: 2000000 INFO @ Sat, 11 Dec 2021 07:00:11: 3000000 INFO @ Sat, 11 Dec 2021 07:00:17: 4000000 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, 11 Dec 2021 07:00:22: #1 tag size is determined as 50 bps INFO @ Sat, 11 Dec 2021 07:00:22: #1 tag size = 50 INFO @ Sat, 11 Dec 2021 07:00:22: #1 total tags in treatment: 4945560 INFO @ Sat, 11 Dec 2021 07:00:22: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 07:00:22: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 11 Dec 2021 07:00:22: #1 tags after filtering in treatment: 4945560 INFO @ Sat, 11 Dec 2021 07:00:22: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 11 Dec 2021 07:00:22: #1 finished! INFO @ Sat, 11 Dec 2021 07:00:22: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 07:00:22: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 07:00:22: #2 number of paired peaks: 49 WARNING @ Sat, 11 Dec 2021 07:00:22: Too few paired peaks (49) 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, 11 Dec 2021 07:00:22: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.10_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/dm3/SRX8689048/SRX8689048.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 11 Dec 2021 07:00:23: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.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 @ Sat, 11 Dec 2021 07:00:23: #1 read tag files... INFO @ Sat, 11 Dec 2021 07:00:23: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 07:00:29: 1000000 INFO @ Sat, 11 Dec 2021 07:00:36: 2000000 INFO @ Sat, 11 Dec 2021 07:00:42: 3000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 11 Dec 2021 07:00:48: 4000000 INFO @ Sat, 11 Dec 2021 07:00:54: #1 tag size is determined as 50 bps INFO @ Sat, 11 Dec 2021 07:00:54: #1 tag size = 50 INFO @ Sat, 11 Dec 2021 07:00:54: #1 total tags in treatment: 4945560 INFO @ Sat, 11 Dec 2021 07:00:54: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 07:00:54: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 11 Dec 2021 07:00:54: #1 tags after filtering in treatment: 4945560 INFO @ Sat, 11 Dec 2021 07:00:54: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 11 Dec 2021 07:00:54: #1 finished! INFO @ Sat, 11 Dec 2021 07:00:54: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 07:00:54: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 07:00:55: #2 number of paired peaks: 49 WARNING @ Sat, 11 Dec 2021 07:00:55: Too few paired peaks (49) 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, 11 Dec 2021 07:00:55: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.20_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/dm3/SRX8689048/SRX8689048.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8689048/SRX8689048.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BigWig に変換しました。