Job ID = 14519739 SRX = SRX9067190 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 8556578 spots for SRR12580343/SRR12580343.sra Written 8556578 spots for SRR12580343/SRR12580343.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: 00:09:48 8556578 reads; of these: 8556578 (100.00%) were paired; of these: 6468937 (75.60%) aligned concordantly 0 times 1632964 (19.08%) aligned concordantly exactly 1 time 454677 (5.31%) aligned concordantly >1 times ---- 6468937 pairs aligned concordantly 0 times; of these: 2420413 (37.42%) aligned discordantly 1 time ---- 4048524 pairs aligned 0 times concordantly or discordantly; of these: 8097048 mates make up the pairs; of these: 6159548 (76.07%) aligned 0 times 315818 (3.90%) aligned exactly 1 time 1621682 (20.03%) aligned >1 times 64.01% overall alignment rate Time searching: 00:09:48 Overall time: 00:09:48 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 8 files... [bam_rmdup_core] processing reference chrI... [bam_rmdup_core] processing reference chrII... [bam_rmdup_core] processing reference chrIII... [bam_rmdup_core] processing reference chrIV... [bam_rmdup_core] processing reference chrIX... [bam_rmdup_core] processing reference chrM... [bam_rmdup_core] processing reference chrV... [bam_rmdup_core] processing reference chrVI... [bam_rmdup_core] processing reference chrVII... [bam_rmdup_core] processing reference chrVIII... [bam_rmdup_core] processing reference chrX... [bam_rmdup_core] processing reference chrXI... [bam_rmdup_core] processing reference chrXII... [bam_rmdup_core] processing reference chrXIII... [bam_rmdup_core] processing reference chrXIV... [bam_rmdup_core] processing reference chrXV... [bam_rmdup_core] processing reference chrXVI... [bam_rmdup_core] 1142144 / 4437107 = 0.2574 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 17:50:27: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.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 17:50:27: #1 read tag files... INFO @ Sat, 15 Jan 2022 17:50:27: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 17:50:34: 1000000 INFO @ Sat, 15 Jan 2022 17:50:42: 2000000 INFO @ Sat, 15 Jan 2022 17:50:49: 3000000 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 17:50:56: 4000000 INFO @ Sat, 15 Jan 2022 17:50:57: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.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 17:50:57: #1 read tag files... INFO @ Sat, 15 Jan 2022 17:50:57: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 17:51:05: 5000000 INFO @ Sat, 15 Jan 2022 17:51:08: 1000000 INFO @ Sat, 15 Jan 2022 17:51:14: 6000000 INFO @ Sat, 15 Jan 2022 17:51:19: 2000000 INFO @ Sat, 15 Jan 2022 17:51:23: 7000000 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 17:51:27: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.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 17:51:27: #1 read tag files... INFO @ Sat, 15 Jan 2022 17:51:27: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 17:51:30: 3000000 INFO @ Sat, 15 Jan 2022 17:51:32: 8000000 INFO @ Sat, 15 Jan 2022 17:51:37: 1000000 INFO @ Sat, 15 Jan 2022 17:51:38: #1 tag size is determined as 151 bps INFO @ Sat, 15 Jan 2022 17:51:38: #1 tag size = 151 INFO @ Sat, 15 Jan 2022 17:51:38: #1 total tags in treatment: 1433429 INFO @ Sat, 15 Jan 2022 17:51:38: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 17:51:38: #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 17:51:38: #1 tags after filtering in treatment: 1123347 INFO @ Sat, 15 Jan 2022 17:51:38: #1 Redundant rate of treatment: 0.22 INFO @ Sat, 15 Jan 2022 17:51:38: #1 finished! INFO @ Sat, 15 Jan 2022 17:51:38: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 17:51:38: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 17:51:38: #2 number of paired peaks: 31 WARNING @ Sat, 15 Jan 2022 17:51:38: 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 17:51:38: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.05_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/SRX9067190/SRX9067190.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 17:51:41: 4000000 INFO @ Sat, 15 Jan 2022 17:51:46: 2000000 INFO @ Sat, 15 Jan 2022 17:51:51: 5000000 INFO @ Sat, 15 Jan 2022 17:51:55: 3000000 INFO @ Sat, 15 Jan 2022 17:52:02: 6000000 INFO @ Sat, 15 Jan 2022 17:52:04: 4000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 17:52:12: 7000000 INFO @ Sat, 15 Jan 2022 17:52:13: 5000000 BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 17:52:22: 6000000 INFO @ Sat, 15 Jan 2022 17:52:23: 8000000 INFO @ Sat, 15 Jan 2022 17:52:30: #1 tag size is determined as 151 bps INFO @ Sat, 15 Jan 2022 17:52:30: #1 tag size = 151 INFO @ Sat, 15 Jan 2022 17:52:30: #1 total tags in treatment: 1433429 INFO @ Sat, 15 Jan 2022 17:52:30: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 17:52:30: #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 17:52:30: #1 tags after filtering in treatment: 1123347 INFO @ Sat, 15 Jan 2022 17:52:30: #1 Redundant rate of treatment: 0.22 INFO @ Sat, 15 Jan 2022 17:52:30: #1 finished! INFO @ Sat, 15 Jan 2022 17:52:30: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 17:52:30: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 17:52:30: #2 number of paired peaks: 31 WARNING @ Sat, 15 Jan 2022 17:52:30: 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 17:52:30: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.10_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/sacCer3/SRX9067190/SRX9067190.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 17:52:31: 7000000 INFO @ Sat, 15 Jan 2022 17:52:39: 8000000 INFO @ Sat, 15 Jan 2022 17:52:45: #1 tag size is determined as 151 bps INFO @ Sat, 15 Jan 2022 17:52:45: #1 tag size = 151 INFO @ Sat, 15 Jan 2022 17:52:45: #1 total tags in treatment: 1433429 INFO @ Sat, 15 Jan 2022 17:52:45: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 17:52:45: #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 17:52:45: #1 tags after filtering in treatment: 1123347 INFO @ Sat, 15 Jan 2022 17:52:45: #1 Redundant rate of treatment: 0.22 INFO @ Sat, 15 Jan 2022 17:52:45: #1 finished! INFO @ Sat, 15 Jan 2022 17:52:45: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 17:52:45: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 17:52:45: #2 number of paired peaks: 31 WARNING @ Sat, 15 Jan 2022 17:52:45: 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 17:52:45: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.20_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/SRX9067190/SRX9067190.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067190/SRX9067190.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling