Job ID = 14167362 SRX = SRX8688933 Genome = dm3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 8429176 spots for SRR12174220/SRR12174220.sra Written 8429176 spots for SRR12174220/SRR12174220.sra fastq に変換しました。 bowtie でマッピング中... Your job 14167985 ("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: 00:02:19 8429176 reads; of these: 8429176 (100.00%) were unpaired; of these: 652940 (7.75%) aligned 0 times 6606052 (78.37%) aligned exactly 1 time 1170184 (13.88%) aligned >1 times 92.25% overall alignment rate Time searching: 00:02:19 Overall time: 00:02:19 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] 367942 / 7776236 = 0.0473 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 12:06:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.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 12:06:04: #1 read tag files... INFO @ Fri, 10 Dec 2021 12:06:04: #1 read treatment tags... INFO @ Fri, 10 Dec 2021 12:06:10: 1000000 INFO @ Fri, 10 Dec 2021 12:06:15: 2000000 INFO @ Fri, 10 Dec 2021 12:06:21: 3000000 INFO @ Fri, 10 Dec 2021 12:06:26: 4000000 INFO @ Fri, 10 Dec 2021 12:06:32: 5000000 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 12:06:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.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 12:06:34: #1 read tag files... INFO @ Fri, 10 Dec 2021 12:06:34: #1 read treatment tags... INFO @ Fri, 10 Dec 2021 12:06:37: 6000000 INFO @ Fri, 10 Dec 2021 12:06:41: 1000000 INFO @ Fri, 10 Dec 2021 12:06:43: 7000000 INFO @ Fri, 10 Dec 2021 12:06:45: #1 tag size is determined as 50 bps INFO @ Fri, 10 Dec 2021 12:06:45: #1 tag size = 50 INFO @ Fri, 10 Dec 2021 12:06:45: #1 total tags in treatment: 7408294 INFO @ Fri, 10 Dec 2021 12:06:45: #1 user defined the maximum tags... INFO @ Fri, 10 Dec 2021 12:06:45: #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 12:06:45: #1 tags after filtering in treatment: 7408294 INFO @ Fri, 10 Dec 2021 12:06:45: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 10 Dec 2021 12:06:45: #1 finished! INFO @ Fri, 10 Dec 2021 12:06:45: #2 Build Peak Model... INFO @ Fri, 10 Dec 2021 12:06:45: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Dec 2021 12:06:46: #2 number of paired peaks: 17 WARNING @ Fri, 10 Dec 2021 12:06:46: Too few paired peaks (17) 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 12:06:46: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.05_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/SRX8688933/SRX8688933.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 10 Dec 2021 12:06:47: 2000000 INFO @ Fri, 10 Dec 2021 12:06:53: 3000000 INFO @ Fri, 10 Dec 2021 12:06:59: 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 @ Fri, 10 Dec 2021 12:07:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.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 12:07:04: #1 read tag files... INFO @ Fri, 10 Dec 2021 12:07:04: #1 read treatment tags... INFO @ Fri, 10 Dec 2021 12:07:05: 5000000 INFO @ Fri, 10 Dec 2021 12:07:10: 1000000 INFO @ Fri, 10 Dec 2021 12:07:11: 6000000 INFO @ Fri, 10 Dec 2021 12:07:15: 2000000 INFO @ Fri, 10 Dec 2021 12:07:18: 7000000 INFO @ Fri, 10 Dec 2021 12:07:21: #1 tag size is determined as 50 bps INFO @ Fri, 10 Dec 2021 12:07:21: #1 tag size = 50 INFO @ Fri, 10 Dec 2021 12:07:21: #1 total tags in treatment: 7408294 INFO @ Fri, 10 Dec 2021 12:07:21: #1 user defined the maximum tags... INFO @ Fri, 10 Dec 2021 12:07:21: #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 12:07:21: #1 tags after filtering in treatment: 7408294 INFO @ Fri, 10 Dec 2021 12:07:21: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 10 Dec 2021 12:07:21: #1 finished! INFO @ Fri, 10 Dec 2021 12:07:21: #2 Build Peak Model... INFO @ Fri, 10 Dec 2021 12:07:21: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Dec 2021 12:07:21: 3000000 INFO @ Fri, 10 Dec 2021 12:07:21: #2 number of paired peaks: 17 WARNING @ Fri, 10 Dec 2021 12:07:21: Too few paired peaks (17) 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 12:07:21: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.10_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/SRX8688933/SRX8688933.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 10 Dec 2021 12:07:27: 4000000 INFO @ Fri, 10 Dec 2021 12:07:32: 5000000 INFO @ Fri, 10 Dec 2021 12:07:38: 6000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Fri, 10 Dec 2021 12:07:43: 7000000 INFO @ Fri, 10 Dec 2021 12:07:45: #1 tag size is determined as 50 bps INFO @ Fri, 10 Dec 2021 12:07:45: #1 tag size = 50 INFO @ Fri, 10 Dec 2021 12:07:45: #1 total tags in treatment: 7408294 INFO @ Fri, 10 Dec 2021 12:07:45: #1 user defined the maximum tags... INFO @ Fri, 10 Dec 2021 12:07:45: #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 12:07:45: #1 tags after filtering in treatment: 7408294 INFO @ Fri, 10 Dec 2021 12:07:45: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 10 Dec 2021 12:07:45: #1 finished! INFO @ Fri, 10 Dec 2021 12:07:45: #2 Build Peak Model... INFO @ Fri, 10 Dec 2021 12:07:45: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Dec 2021 12:07:46: #2 number of paired peaks: 17 WARNING @ Fri, 10 Dec 2021 12:07:46: Too few paired peaks (17) 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 12:07:46: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.20_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/SRX8688933/SRX8688933.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX8688933/SRX8688933.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BigWig に変換しました。