Job ID = 7113557 SRX = SRX8462173 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2020-07-22T05:40:15 prefetch.2.10.7: 1) Downloading 'SRR11915632'... 2020-07-22T05:40:15 prefetch.2.10.7: Downloading via HTTPS... 2020-07-22T05:42:29 prefetch.2.10.7: HTTPS download succeed 2020-07-22T05:42:30 prefetch.2.10.7: 'SRR11915632' is valid 2020-07-22T05:42:30 prefetch.2.10.7: 1) 'SRR11915632' was downloaded successfully 2020-07-22T05:42:30 prefetch.2.10.7: 'SRR11915632' has 0 unresolved dependencies Read 7486791 spots for SRR11915632/SRR11915632.sra Written 7486791 spots for SRR11915632/SRR11915632.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: 00:06:24 7486791 reads; of these: 7486791 (100.00%) were paired; of these: 1022256 (13.65%) aligned concordantly 0 times 5475574 (73.14%) aligned concordantly exactly 1 time 988961 (13.21%) aligned concordantly >1 times ---- 1022256 pairs aligned concordantly 0 times; of these: 58859 (5.76%) aligned discordantly 1 time ---- 963397 pairs aligned 0 times concordantly or discordantly; of these: 1926794 mates make up the pairs; of these: 1755457 (91.11%) aligned 0 times 122337 (6.35%) aligned exactly 1 time 49000 (2.54%) aligned >1 times 88.28% overall alignment rate Time searching: 00:06:24 Overall time: 00:06:24 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] 3022504 / 6519166 = 0.4636 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 14:53:43: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.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 14:53:43: #1 read tag files... INFO @ Wed, 22 Jul 2020 14:53:43: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 14:53:49: 1000000 INFO @ Wed, 22 Jul 2020 14:53:55: 2000000 INFO @ Wed, 22 Jul 2020 14:54:02: 3000000 INFO @ Wed, 22 Jul 2020 14:54:08: 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 14:54:12: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.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 14:54:12: #1 read tag files... INFO @ Wed, 22 Jul 2020 14:54:12: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 14:54:15: 5000000 INFO @ Wed, 22 Jul 2020 14:54:19: 1000000 INFO @ Wed, 22 Jul 2020 14:54:21: 6000000 INFO @ Wed, 22 Jul 2020 14:54:25: 2000000 INFO @ Wed, 22 Jul 2020 14:54:27: 7000000 INFO @ Wed, 22 Jul 2020 14:54:28: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 14:54:28: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 14:54:28: #1 total tags in treatment: 3451994 INFO @ Wed, 22 Jul 2020 14:54:28: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 14:54:28: #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 14:54:28: #1 tags after filtering in treatment: 2590868 INFO @ Wed, 22 Jul 2020 14:54:28: #1 Redundant rate of treatment: 0.25 INFO @ Wed, 22 Jul 2020 14:54:28: #1 finished! INFO @ Wed, 22 Jul 2020 14:54:28: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 14:54:28: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 14:54:29: #2 number of paired peaks: 49 WARNING @ Wed, 22 Jul 2020 14:54:29: Too few paired peaks (49) 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 14:54:29: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.05_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/SRX8462173/SRX8462173.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Wed, 22 Jul 2020 14:54:32: 3000000 INFO @ Wed, 22 Jul 2020 14:54:38: 4000000 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 14:54:42: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.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 14:54:42: #1 read tag files... INFO @ Wed, 22 Jul 2020 14:54:42: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 14:54:45: 5000000 INFO @ Wed, 22 Jul 2020 14:54:49: 1000000 INFO @ Wed, 22 Jul 2020 14:54:51: 6000000 INFO @ Wed, 22 Jul 2020 14:54:55: 2000000 INFO @ Wed, 22 Jul 2020 14:54:57: 7000000 INFO @ Wed, 22 Jul 2020 14:54:58: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 14:54:58: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 14:54:58: #1 total tags in treatment: 3451994 INFO @ Wed, 22 Jul 2020 14:54:58: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 14:54:58: #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 14:54:58: #1 tags after filtering in treatment: 2590868 INFO @ Wed, 22 Jul 2020 14:54:58: #1 Redundant rate of treatment: 0.25 INFO @ Wed, 22 Jul 2020 14:54:58: #1 finished! INFO @ Wed, 22 Jul 2020 14:54:58: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 14:54:58: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 14:54:59: #2 number of paired peaks: 49 WARNING @ Wed, 22 Jul 2020 14:54:59: Too few paired peaks (49) 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 14:54:59: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.10_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/SRX8462173/SRX8462173.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Wed, 22 Jul 2020 14:55:01: 3000000 INFO @ Wed, 22 Jul 2020 14:55:08: 4000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Wed, 22 Jul 2020 14:55:14: 5000000 INFO @ Wed, 22 Jul 2020 14:55:20: 6000000 BigWig に変換しました。 INFO @ Wed, 22 Jul 2020 14:55:26: 7000000 INFO @ Wed, 22 Jul 2020 14:55:27: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 14:55:27: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 14:55:27: #1 total tags in treatment: 3451994 INFO @ Wed, 22 Jul 2020 14:55:27: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 14:55:27: #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 14:55:27: #1 tags after filtering in treatment: 2590868 INFO @ Wed, 22 Jul 2020 14:55:27: #1 Redundant rate of treatment: 0.25 INFO @ Wed, 22 Jul 2020 14:55:27: #1 finished! INFO @ Wed, 22 Jul 2020 14:55:27: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 14:55:27: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 14:55:27: #2 number of paired peaks: 49 WARNING @ Wed, 22 Jul 2020 14:55:27: Too few paired peaks (49) 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 14:55:27: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.20_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/SRX8462173/SRX8462173.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462173/SRX8462173.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling