Job ID = 14521186 SRX = SRX9431298 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 8775231 spots for SRR12979591/SRR12979591.sra Written 8775231 spots for SRR12979591/SRR12979591.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: 00:01:57 8775231 reads; of these: 8775231 (100.00%) were unpaired; of these: 458964 (5.23%) aligned 0 times 7362715 (83.90%) aligned exactly 1 time 953552 (10.87%) aligned >1 times 94.77% overall alignment rate Time searching: 00:01:57 Overall time: 00:01:57 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_rmdupse_core] 2496553 / 8316267 = 0.3002 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 20:39:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.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 20:39:02: #1 read tag files... INFO @ Sat, 15 Jan 2022 20:39:02: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 20:39:07: 1000000 INFO @ Sat, 15 Jan 2022 20:39:13: 2000000 INFO @ Sat, 15 Jan 2022 20:39:19: 3000000 INFO @ Sat, 15 Jan 2022 20:39:25: 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 20:39:31: 5000000 INFO @ Sat, 15 Jan 2022 20:39:32: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.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 20:39:32: #1 read tag files... INFO @ Sat, 15 Jan 2022 20:39:32: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 20:39:37: #1 tag size is determined as 82 bps INFO @ Sat, 15 Jan 2022 20:39:37: #1 tag size = 82 INFO @ Sat, 15 Jan 2022 20:39:37: #1 total tags in treatment: 5819714 INFO @ Sat, 15 Jan 2022 20:39:37: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 20:39:37: #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 20:39:37: #1 tags after filtering in treatment: 5819714 INFO @ Sat, 15 Jan 2022 20:39:37: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 20:39:37: #1 finished! INFO @ Sat, 15 Jan 2022 20:39:37: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 20:39:37: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 20:39:37: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 20:39:37: 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 20:39:37: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.05_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/sacCer3/SRX9431298/SRX9431298.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 20:39:40: 1000000 INFO @ Sat, 15 Jan 2022 20:39:48: 2000000 INFO @ Sat, 15 Jan 2022 20:39:56: 3000000 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 20:40:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.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 20:40:02: #1 read tag files... INFO @ Sat, 15 Jan 2022 20:40:02: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 20:40:04: 4000000 INFO @ Sat, 15 Jan 2022 20:40:09: 1000000 INFO @ Sat, 15 Jan 2022 20:40:12: 5000000 INFO @ Sat, 15 Jan 2022 20:40:18: 2000000 INFO @ Sat, 15 Jan 2022 20:40:19: #1 tag size is determined as 82 bps INFO @ Sat, 15 Jan 2022 20:40:19: #1 tag size = 82 INFO @ Sat, 15 Jan 2022 20:40:19: #1 total tags in treatment: 5819714 INFO @ Sat, 15 Jan 2022 20:40:19: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 20:40:19: #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 20:40:19: #1 tags after filtering in treatment: 5819714 INFO @ Sat, 15 Jan 2022 20:40:19: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 20:40:19: #1 finished! INFO @ Sat, 15 Jan 2022 20:40:19: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 20:40:19: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 20:40:20: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 20:40:20: 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 20:40:20: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.10_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/SRX9431298/SRX9431298.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 20:40:24: 3000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 20:40:30: 4000000 BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 20:40:36: 5000000 INFO @ Sat, 15 Jan 2022 20:40:41: #1 tag size is determined as 82 bps INFO @ Sat, 15 Jan 2022 20:40:41: #1 tag size = 82 INFO @ Sat, 15 Jan 2022 20:40:41: #1 total tags in treatment: 5819714 INFO @ Sat, 15 Jan 2022 20:40:41: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 20:40:41: #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 20:40:41: #1 tags after filtering in treatment: 5819714 INFO @ Sat, 15 Jan 2022 20:40:41: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 20:40:41: #1 finished! INFO @ Sat, 15 Jan 2022 20:40:41: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 20:40:41: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 20:40:41: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 20:40:41: 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 20:40:41: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.20_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/SRX9431298/SRX9431298.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9431298/SRX9431298.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling