Job ID = 7115571 SRX = SRX8462240 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2020-07-22T06:10:48 prefetch.2.10.7: 1) Downloading 'SRR11915699'... 2020-07-22T06:10:48 prefetch.2.10.7: Downloading via HTTPS... 2020-07-22T06:11:19 prefetch.2.10.7: HTTPS download succeed 2020-07-22T06:11:19 prefetch.2.10.7: 'SRR11915699' is valid 2020-07-22T06:11:19 prefetch.2.10.7: 1) 'SRR11915699' was downloaded successfully 2020-07-22T06:11:19 prefetch.2.10.7: 'SRR11915699' has 0 unresolved dependencies Read 2473531 spots for SRR11915699/SRR11915699.sra Written 2473531 spots for SRR11915699/SRR11915699.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: 00:02:05 2473531 reads; of these: 2473531 (100.00%) were paired; of these: 140181 (5.67%) aligned concordantly 0 times 2026166 (81.91%) aligned concordantly exactly 1 time 307184 (12.42%) aligned concordantly >1 times ---- 140181 pairs aligned concordantly 0 times; of these: 12009 (8.57%) aligned discordantly 1 time ---- 128172 pairs aligned 0 times concordantly or discordantly; of these: 256344 mates make up the pairs; of these: 196546 (76.67%) aligned 0 times 47809 (18.65%) aligned exactly 1 time 11989 (4.68%) aligned >1 times 96.03% overall alignment rate Time searching: 00:02:05 Overall time: 00:02:05 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_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] 223565 / 2339579 = 0.0956 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 15:15:46: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.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 15:15:46: #1 read tag files... INFO @ Wed, 22 Jul 2020 15:15:46: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 15:15:51: 1000000 INFO @ Wed, 22 Jul 2020 15:15:56: 2000000 INFO @ Wed, 22 Jul 2020 15:16:01: 3000000 INFO @ Wed, 22 Jul 2020 15:16:06: 4000000 INFO @ Wed, 22 Jul 2020 15:16:08: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 15:16:08: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 15:16:08: #1 total tags in treatment: 2110039 INFO @ Wed, 22 Jul 2020 15:16:08: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 15:16:08: #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 15:16:08: #1 tags after filtering in treatment: 1865145 INFO @ Wed, 22 Jul 2020 15:16:08: #1 Redundant rate of treatment: 0.12 INFO @ Wed, 22 Jul 2020 15:16:08: #1 finished! INFO @ Wed, 22 Jul 2020 15:16:08: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 15:16:08: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 15:16:08: #2 number of paired peaks: 76 WARNING @ Wed, 22 Jul 2020 15:16:08: Too few paired peaks (76) 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 15:16:08: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.05_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/SRX8462240/SRX8462240.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling 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 15:16:16: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.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 15:16:16: #1 read tag files... INFO @ Wed, 22 Jul 2020 15:16:16: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 15:16:21: 1000000 INFO @ Wed, 22 Jul 2020 15:16:26: 2000000 INFO @ Wed, 22 Jul 2020 15:16:31: 3000000 INFO @ Wed, 22 Jul 2020 15:16:37: 4000000 INFO @ Wed, 22 Jul 2020 15:16:38: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 15:16:38: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 15:16:38: #1 total tags in treatment: 2110039 INFO @ Wed, 22 Jul 2020 15:16:38: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 15:16:38: #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 15:16:38: #1 tags after filtering in treatment: 1865145 INFO @ Wed, 22 Jul 2020 15:16:38: #1 Redundant rate of treatment: 0.12 INFO @ Wed, 22 Jul 2020 15:16:38: #1 finished! INFO @ Wed, 22 Jul 2020 15:16:38: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 15:16:38: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 15:16:38: #2 number of paired peaks: 76 WARNING @ Wed, 22 Jul 2020 15:16:38: Too few paired peaks (76) 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 15:16:38: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.10_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/SRX8462240/SRX8462240.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling 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 15:16:46: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.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 15:16:46: #1 read tag files... INFO @ Wed, 22 Jul 2020 15:16:46: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 15:16:51: 1000000 INFO @ Wed, 22 Jul 2020 15:16:56: 2000000 INFO @ Wed, 22 Jul 2020 15:17:01: 3000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Wed, 22 Jul 2020 15:17:07: 4000000 INFO @ Wed, 22 Jul 2020 15:17:08: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 15:17:08: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 15:17:08: #1 total tags in treatment: 2110039 INFO @ Wed, 22 Jul 2020 15:17:08: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 15:17:08: #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 15:17:08: #1 tags after filtering in treatment: 1865145 INFO @ Wed, 22 Jul 2020 15:17:08: #1 Redundant rate of treatment: 0.12 INFO @ Wed, 22 Jul 2020 15:17:08: #1 finished! INFO @ Wed, 22 Jul 2020 15:17:08: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 15:17:08: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 15:17:09: #2 number of paired peaks: 76 WARNING @ Wed, 22 Jul 2020 15:17:09: Too few paired peaks (76) 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 15:17:09: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.20_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/SRX8462240/SRX8462240.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462240/SRX8462240.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BigWig に変換しました。