Job ID = 7113818 SRX = SRX8462182 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2020-07-22T05:46:11 prefetch.2.10.7: 1) Downloading 'SRR11915641'... 2020-07-22T05:46:11 prefetch.2.10.7: Downloading via HTTPS... 2020-07-22T05:47:37 prefetch.2.10.7: HTTPS download succeed 2020-07-22T05:47:38 prefetch.2.10.7: 'SRR11915641' is valid 2020-07-22T05:47:38 prefetch.2.10.7: 1) 'SRR11915641' was downloaded successfully 2020-07-22T05:47:38 prefetch.2.10.7: 'SRR11915641' has 0 unresolved dependencies Read 6219715 spots for SRR11915641/SRR11915641.sra Written 6219715 spots for SRR11915641/SRR11915641.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: 00:05:34 6219715 reads; of these: 6219715 (100.00%) were paired; of these: 1043397 (16.78%) aligned concordantly 0 times 4280996 (68.83%) aligned concordantly exactly 1 time 895322 (14.39%) aligned concordantly >1 times ---- 1043397 pairs aligned concordantly 0 times; of these: 47888 (4.59%) aligned discordantly 1 time ---- 995509 pairs aligned 0 times concordantly or discordantly; of these: 1991018 mates make up the pairs; of these: 1859253 (93.38%) aligned 0 times 90690 (4.55%) aligned exactly 1 time 41075 (2.06%) aligned >1 times 85.05% overall alignment rate Time searching: 00:05:34 Overall time: 00:05:34 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] 2510032 / 5221274 = 0.4807 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 14:57:10: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.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 14:57:10: #1 read tag files... INFO @ Wed, 22 Jul 2020 14:57:10: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 14:57:17: 1000000 INFO @ Wed, 22 Jul 2020 14:57:25: 2000000 INFO @ Wed, 22 Jul 2020 14:57:33: 3000000 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 14:57:40: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.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 14:57:40: #1 read tag files... INFO @ Wed, 22 Jul 2020 14:57:40: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 14:57:41: 4000000 INFO @ Wed, 22 Jul 2020 14:57:47: 1000000 INFO @ Wed, 22 Jul 2020 14:57:50: 5000000 INFO @ Wed, 22 Jul 2020 14:57:55: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 14:57:55: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 14:57:55: #1 total tags in treatment: 2674961 INFO @ Wed, 22 Jul 2020 14:57:55: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 14:57:55: #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 14:57:55: #1 tags after filtering in treatment: 2015978 INFO @ Wed, 22 Jul 2020 14:57:55: #1 Redundant rate of treatment: 0.25 INFO @ Wed, 22 Jul 2020 14:57:55: #1 finished! INFO @ Wed, 22 Jul 2020 14:57:55: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 14:57:55: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 14:57:55: #2 number of paired peaks: 81 WARNING @ Wed, 22 Jul 2020 14:57:55: Too few paired peaks (81) 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 14:57:55: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.05_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/SRX8462182/SRX8462182.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Wed, 22 Jul 2020 14:57:55: 2000000 INFO @ Wed, 22 Jul 2020 14:58:02: 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 14:58:09: 4000000 INFO @ Wed, 22 Jul 2020 14:58:09: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.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 14:58:09: #1 read tag files... INFO @ Wed, 22 Jul 2020 14:58:09: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 14:58:17: 5000000 INFO @ Wed, 22 Jul 2020 14:58:18: 1000000 INFO @ Wed, 22 Jul 2020 14:58:21: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 14:58:21: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 14:58:21: #1 total tags in treatment: 2674961 INFO @ Wed, 22 Jul 2020 14:58:21: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 14:58:21: #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 14:58:21: #1 tags after filtering in treatment: 2015978 INFO @ Wed, 22 Jul 2020 14:58:21: #1 Redundant rate of treatment: 0.25 INFO @ Wed, 22 Jul 2020 14:58:21: #1 finished! INFO @ Wed, 22 Jul 2020 14:58:21: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 14:58:21: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 14:58:22: #2 number of paired peaks: 81 WARNING @ Wed, 22 Jul 2020 14:58:22: Too few paired peaks (81) 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 14:58:22: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.10_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/SRX8462182/SRX8462182.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Wed, 22 Jul 2020 14:58:26: 2000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Wed, 22 Jul 2020 14:58:34: 3000000 BigWig に変換しました。 INFO @ Wed, 22 Jul 2020 14:58:42: 4000000 INFO @ Wed, 22 Jul 2020 14:58:50: 5000000 INFO @ Wed, 22 Jul 2020 14:58:54: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 14:58:54: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 14:58:54: #1 total tags in treatment: 2674961 INFO @ Wed, 22 Jul 2020 14:58:54: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 14:58:54: #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 14:58:54: #1 tags after filtering in treatment: 2015978 INFO @ Wed, 22 Jul 2020 14:58:54: #1 Redundant rate of treatment: 0.25 INFO @ Wed, 22 Jul 2020 14:58:54: #1 finished! INFO @ Wed, 22 Jul 2020 14:58:54: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 14:58:54: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 14:58:54: #2 number of paired peaks: 81 WARNING @ Wed, 22 Jul 2020 14:58:54: Too few paired peaks (81) 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 14:58:54: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.20_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/SRX8462182/SRX8462182.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462182/SRX8462182.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling