Job ID = 12265991 SRX = SRX7282626 Genome = dm3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 5740 spots for SRR10603073/SRR10603073.sra Written 5740 spots for SRR10603073/SRR10603073.sra fastq に変換しました。 bowtie でマッピング中... Your job 12266097 ("srTdm6") has been submitted Time loading reference: 00:00:00 Time loading forward index: 00:00:01 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:00:00 5740 reads; of these: 5740 (100.00%) were unpaired; of these: 679 (11.83%) aligned 0 times 182 (3.17%) aligned exactly 1 time 4879 (85.00%) aligned >1 times 88.17% overall alignment rate Time searching: 00:00:01 Overall time: 00:00:01 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] 4264 / 5061 = 0.8425 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/3.7.1/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 03 Apr 2021 08:42:15: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.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, 03 Apr 2021 08:42:15: #1 read tag files... INFO @ Sat, 03 Apr 2021 08:42:15: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 08:42:15: #1 tag size is determined as 54 bps INFO @ Sat, 03 Apr 2021 08:42:15: #1 tag size = 54 INFO @ Sat, 03 Apr 2021 08:42:15: #1 total tags in treatment: 797 INFO @ Sat, 03 Apr 2021 08:42:15: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 08:42:15: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 03 Apr 2021 08:42:15: #1 tags after filtering in treatment: 790 INFO @ Sat, 03 Apr 2021 08:42:15: #1 Redundant rate of treatment: 0.01 INFO @ Sat, 03 Apr 2021 08:42:15: #1 finished! INFO @ Sat, 03 Apr 2021 08:42:15: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 08:42:15: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 08:42:15: #2 number of paired peaks: 0 WARNING @ Sat, 03 Apr 2021 08:42:15: 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, 03 Apr 2021 08:42:15: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.05_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/SRX7282626/SRX7282626.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling WARNING: Skipping mount /opt/pkg/singularity/3.7.1/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 03 Apr 2021 08:42:45: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.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, 03 Apr 2021 08:42:45: #1 read tag files... INFO @ Sat, 03 Apr 2021 08:42:45: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 08:42:45: #1 tag size is determined as 54 bps INFO @ Sat, 03 Apr 2021 08:42:45: #1 tag size = 54 INFO @ Sat, 03 Apr 2021 08:42:45: #1 total tags in treatment: 797 INFO @ Sat, 03 Apr 2021 08:42:45: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 08:42:45: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 03 Apr 2021 08:42:45: #1 tags after filtering in treatment: 790 INFO @ Sat, 03 Apr 2021 08:42:45: #1 Redundant rate of treatment: 0.01 INFO @ Sat, 03 Apr 2021 08:42:45: #1 finished! INFO @ Sat, 03 Apr 2021 08:42:45: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 08:42:45: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 08:42:45: #2 number of paired peaks: 0 WARNING @ Sat, 03 Apr 2021 08:42:45: 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, 03 Apr 2021 08:42:45: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.10_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/SRX7282626/SRX7282626.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.7.1/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 INFO @ Sat, 03 Apr 2021 08:43:15: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.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, 03 Apr 2021 08:43:15: #1 read tag files... INFO @ Sat, 03 Apr 2021 08:43:15: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 08:43:15: #1 tag size is determined as 54 bps INFO @ Sat, 03 Apr 2021 08:43:15: #1 tag size = 54 INFO @ Sat, 03 Apr 2021 08:43:15: #1 total tags in treatment: 797 INFO @ Sat, 03 Apr 2021 08:43:15: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 08:43:15: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 03 Apr 2021 08:43:15: #1 tags after filtering in treatment: 790 INFO @ Sat, 03 Apr 2021 08:43:15: #1 Redundant rate of treatment: 0.01 INFO @ Sat, 03 Apr 2021 08:43:15: #1 finished! INFO @ Sat, 03 Apr 2021 08:43:15: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 08:43:15: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 08:43:15: #2 number of paired peaks: 0 WARNING @ Sat, 03 Apr 2021 08:43:15: 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, 03 Apr 2021 08:43:15: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.20_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/SRX7282626/SRX7282626.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7282626/SRX7282626.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling