Job ID = 7113599 SRX = SRX8462176 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2020-07-22T05:42:37 prefetch.2.10.7: 1) Downloading 'SRR11915635'... 2020-07-22T05:42:37 prefetch.2.10.7: Downloading via HTTPS... 2020-07-22T05:43:36 prefetch.2.10.7: HTTPS download succeed 2020-07-22T05:43:36 prefetch.2.10.7: 'SRR11915635' is valid 2020-07-22T05:43:36 prefetch.2.10.7: 1) 'SRR11915635' was downloaded successfully 2020-07-22T05:43:36 prefetch.2.10.7: 'SRR11915635' has 0 unresolved dependencies Read 5443086 spots for SRR11915635/SRR11915635.sra Written 5443086 spots for SRR11915635/SRR11915635.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: 00:04:51 5443086 reads; of these: 5443086 (100.00%) were paired; of these: 596554 (10.96%) aligned concordantly 0 times 3973780 (73.01%) aligned concordantly exactly 1 time 872752 (16.03%) aligned concordantly >1 times ---- 596554 pairs aligned concordantly 0 times; of these: 18657 (3.13%) aligned discordantly 1 time ---- 577897 pairs aligned 0 times concordantly or discordantly; of these: 1155794 mates make up the pairs; of these: 1041194 (90.08%) aligned 0 times 84127 (7.28%) aligned exactly 1 time 30473 (2.64%) aligned >1 times 90.44% overall alignment rate Time searching: 00:04:51 Overall time: 00:04:51 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] 1255527 / 4861503 = 0.2583 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/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Wed, 22 Jul 2020 14:52:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.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 @ Wed, 22 Jul 2020 14:52:30: #1 read tag files... INFO @ Wed, 22 Jul 2020 14:52:30: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 14:52:36: 1000000 INFO @ Wed, 22 Jul 2020 14:52:42: 2000000 INFO @ Wed, 22 Jul 2020 14:52:48: 3000000 INFO @ Wed, 22 Jul 2020 14:52:54: 4000000 WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Wed, 22 Jul 2020 14:53:00: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.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 @ Wed, 22 Jul 2020 14:53:00: #1 read tag files... INFO @ Wed, 22 Jul 2020 14:53:00: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 14:53:00: 5000000 INFO @ Wed, 22 Jul 2020 14:53:07: 6000000 INFO @ Wed, 22 Jul 2020 14:53:08: 1000000 INFO @ Wed, 22 Jul 2020 14:53:15: 7000000 INFO @ Wed, 22 Jul 2020 14:53:16: 2000000 INFO @ Wed, 22 Jul 2020 14:53:17: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 14:53:17: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 14:53:17: #1 total tags in treatment: 3592013 INFO @ Wed, 22 Jul 2020 14:53:17: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 14:53:17: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Jul 2020 14:53:17: #1 tags after filtering in treatment: 2740905 INFO @ Wed, 22 Jul 2020 14:53:17: #1 Redundant rate of treatment: 0.24 INFO @ Wed, 22 Jul 2020 14:53:17: #1 finished! INFO @ Wed, 22 Jul 2020 14:53:17: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 14:53:17: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 14:53:17: #2 number of paired peaks: 34 WARNING @ Wed, 22 Jul 2020 14:53:17: Too few paired peaks (34) 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 @ Wed, 22 Jul 2020 14:53:17: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.05_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/SRX8462176/SRX8462176.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Wed, 22 Jul 2020 14:53:23: 3000000 BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Wed, 22 Jul 2020 14:53:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.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 @ Wed, 22 Jul 2020 14:53:30: #1 read tag files... INFO @ Wed, 22 Jul 2020 14:53:30: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 14:53:30: 4000000 INFO @ Wed, 22 Jul 2020 14:53:38: 5000000 INFO @ Wed, 22 Jul 2020 14:53:38: 1000000 INFO @ Wed, 22 Jul 2020 14:53:45: 6000000 INFO @ Wed, 22 Jul 2020 14:53:46: 2000000 INFO @ Wed, 22 Jul 2020 14:53:53: 7000000 INFO @ Wed, 22 Jul 2020 14:53:54: 3000000 INFO @ Wed, 22 Jul 2020 14:53:55: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 14:53:55: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 14:53:55: #1 total tags in treatment: 3592013 INFO @ Wed, 22 Jul 2020 14:53:55: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 14:53:55: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Jul 2020 14:53:55: #1 tags after filtering in treatment: 2740905 INFO @ Wed, 22 Jul 2020 14:53:55: #1 Redundant rate of treatment: 0.24 INFO @ Wed, 22 Jul 2020 14:53:55: #1 finished! INFO @ Wed, 22 Jul 2020 14:53:55: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 14:53:55: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 14:53:56: #2 number of paired peaks: 34 WARNING @ Wed, 22 Jul 2020 14:53:56: Too few paired peaks (34) 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 @ Wed, 22 Jul 2020 14:53:56: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.10_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/SRX8462176/SRX8462176.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... INFO @ Wed, 22 Jul 2020 14:54:01: 4000000 INFO @ Wed, 22 Jul 2020 14:54:09: 5000000 BigWig に変換しました。 INFO @ Wed, 22 Jul 2020 14:54:16: 6000000 INFO @ Wed, 22 Jul 2020 14:54:24: 7000000 INFO @ Wed, 22 Jul 2020 14:54:26: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 14:54:26: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 14:54:26: #1 total tags in treatment: 3592013 INFO @ Wed, 22 Jul 2020 14:54:26: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 14:54:26: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Jul 2020 14:54:26: #1 tags after filtering in treatment: 2740905 INFO @ Wed, 22 Jul 2020 14:54:26: #1 Redundant rate of treatment: 0.24 INFO @ Wed, 22 Jul 2020 14:54:26: #1 finished! INFO @ Wed, 22 Jul 2020 14:54:26: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 14:54:26: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 14:54:26: #2 number of paired peaks: 34 WARNING @ Wed, 22 Jul 2020 14:54:26: Too few paired peaks (34) 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 @ Wed, 22 Jul 2020 14:54:26: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.20_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/SRX8462176/SRX8462176.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462176/SRX8462176.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling