Job ID = 14519795 SRX = ERX4107468 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 34257347 spots for ERR4140177/ERR4140177.sra Written 34257347 spots for ERR4140177/ERR4140177.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: 00:05:02 34257347 reads; of these: 34257347 (100.00%) were unpaired; of these: 10437467 (30.47%) aligned 0 times 20480859 (59.79%) aligned exactly 1 time 3339021 (9.75%) aligned >1 times 69.53% overall alignment rate Time searching: 00:05:02 Overall time: 00:05:02 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_sort_core] merging from 12 files... [bam_rmdupse_core] 19807428 / 23819880 = 0.8316 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 17:57:50: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.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 17:57:50: #1 read tag files... INFO @ Sat, 15 Jan 2022 17:57:50: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 17:57:56: 1000000 INFO @ Sat, 15 Jan 2022 17:58:01: 2000000 INFO @ Sat, 15 Jan 2022 17:58:07: 3000000 INFO @ Sat, 15 Jan 2022 17:58:13: 4000000 INFO @ Sat, 15 Jan 2022 17:58:13: #1 tag size is determined as 50 bps INFO @ Sat, 15 Jan 2022 17:58:13: #1 tag size = 50 INFO @ Sat, 15 Jan 2022 17:58:13: #1 total tags in treatment: 4012452 INFO @ Sat, 15 Jan 2022 17:58:13: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 17:58:13: #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 17:58:13: #1 tags after filtering in treatment: 4012452 INFO @ Sat, 15 Jan 2022 17:58:13: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 17:58:13: #1 finished! INFO @ Sat, 15 Jan 2022 17:58:13: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 17:58:13: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 17:58:13: #2 number of paired peaks: 31 WARNING @ Sat, 15 Jan 2022 17:58:13: Too few paired peaks (31) 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 17:58:13: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.05_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/sacCer3/ERX4107468/ERX4107468.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.05_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, 15 Jan 2022 17:58:20: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.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 17:58:20: #1 read tag files... INFO @ Sat, 15 Jan 2022 17:58:20: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 17:58:25: 1000000 INFO @ Sat, 15 Jan 2022 17:58:31: 2000000 INFO @ Sat, 15 Jan 2022 17:58:36: 3000000 INFO @ Sat, 15 Jan 2022 17:58:41: 4000000 INFO @ Sat, 15 Jan 2022 17:58:41: #1 tag size is determined as 50 bps INFO @ Sat, 15 Jan 2022 17:58:41: #1 tag size = 50 INFO @ Sat, 15 Jan 2022 17:58:41: #1 total tags in treatment: 4012452 INFO @ Sat, 15 Jan 2022 17:58:41: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 17:58:41: #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 17:58:41: #1 tags after filtering in treatment: 4012452 INFO @ Sat, 15 Jan 2022 17:58:41: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 17:58:41: #1 finished! INFO @ Sat, 15 Jan 2022 17:58:41: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 17:58:41: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 17:58:42: #2 number of paired peaks: 31 WARNING @ Sat, 15 Jan 2022 17:58:42: Too few paired peaks (31) 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 17:58:42: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.10_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/ERX4107468/ERX4107468.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.10_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 @ Sat, 15 Jan 2022 17:58:50: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.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 17:58:50: #1 read tag files... INFO @ Sat, 15 Jan 2022 17:58:50: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 17:58:55: 1000000 INFO @ Sat, 15 Jan 2022 17:59:01: 2000000 INFO @ Sat, 15 Jan 2022 17:59:06: 3000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 17:59:12: 4000000 INFO @ Sat, 15 Jan 2022 17:59:12: #1 tag size is determined as 50 bps INFO @ Sat, 15 Jan 2022 17:59:12: #1 tag size = 50 INFO @ Sat, 15 Jan 2022 17:59:12: #1 total tags in treatment: 4012452 INFO @ Sat, 15 Jan 2022 17:59:12: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 17:59:12: #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 17:59:12: #1 tags after filtering in treatment: 4012452 INFO @ Sat, 15 Jan 2022 17:59:12: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 17:59:12: #1 finished! INFO @ Sat, 15 Jan 2022 17:59:12: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 17:59:12: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 17:59:12: #2 number of paired peaks: 31 WARNING @ Sat, 15 Jan 2022 17:59:12: Too few paired peaks (31) 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 17:59:12: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.20_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/ERX4107468/ERX4107468.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4107468/ERX4107468.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BigWig に変換しました。