Job ID = 5791728 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... spots read : 5,364,400 reads read : 10,728,800 reads written : 10,728,800 rm: cannot remove ‘[DSE]RR*’: No such file or directory 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: 00:02:08 5364400 reads; of these: 5364400 (100.00%) were paired; of these: 251297 (4.68%) aligned concordantly 0 times 4426328 (82.51%) aligned concordantly exactly 1 time 686775 (12.80%) aligned concordantly >1 times ---- 251297 pairs aligned concordantly 0 times; of these: 20973 (8.35%) aligned discordantly 1 time ---- 230324 pairs aligned 0 times concordantly or discordantly; of these: 460648 mates make up the pairs; of these: 424169 (92.08%) aligned 0 times 24462 (5.31%) aligned exactly 1 time 12017 (2.61%) aligned >1 times 96.05% overall alignment rate Time searching: 00:02:08 Overall time: 00:02:08 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] 180921 / 5132415 = 0.0353 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 Apr 2020 10:43:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.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 Apr 2020 10:43:30: #1 read tag files... INFO @ Wed, 22 Apr 2020 10:43:30: #1 read treatment tags... INFO @ Wed, 22 Apr 2020 10:43:35: 1000000 INFO @ Wed, 22 Apr 2020 10:43:39: 2000000 INFO @ Wed, 22 Apr 2020 10:43:44: 3000000 INFO @ Wed, 22 Apr 2020 10:43:49: 4000000 INFO @ Wed, 22 Apr 2020 10:43:53: 5000000 INFO @ Wed, 22 Apr 2020 10:43:58: 6000000 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 Apr 2020 10:44:00: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.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 Apr 2020 10:44:00: #1 read tag files... INFO @ Wed, 22 Apr 2020 10:44:00: #1 read treatment tags... INFO @ Wed, 22 Apr 2020 10:44:03: 7000000 INFO @ Wed, 22 Apr 2020 10:44:05: 1000000 INFO @ Wed, 22 Apr 2020 10:44:08: 8000000 INFO @ Wed, 22 Apr 2020 10:44:11: 2000000 INFO @ Wed, 22 Apr 2020 10:44:14: 9000000 INFO @ Wed, 22 Apr 2020 10:44:16: 3000000 INFO @ Wed, 22 Apr 2020 10:44:19: #1 tag size is determined as 38 bps INFO @ Wed, 22 Apr 2020 10:44:19: #1 tag size = 38 INFO @ Wed, 22 Apr 2020 10:44:19: #1 total tags in treatment: 4932555 INFO @ Wed, 22 Apr 2020 10:44:19: #1 user defined the maximum tags... INFO @ Wed, 22 Apr 2020 10:44:19: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Apr 2020 10:44:19: #1 tags after filtering in treatment: 3957646 INFO @ Wed, 22 Apr 2020 10:44:19: #1 Redundant rate of treatment: 0.20 INFO @ Wed, 22 Apr 2020 10:44:19: #1 finished! INFO @ Wed, 22 Apr 2020 10:44:19: #2 Build Peak Model... INFO @ Wed, 22 Apr 2020 10:44:19: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Apr 2020 10:44:19: #2 number of paired peaks: 75 WARNING @ Wed, 22 Apr 2020 10:44:19: Too few paired peaks (75) 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 Apr 2020 10:44:19: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.05_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/SRX7741020/SRX7741020.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Wed, 22 Apr 2020 10:44:21: 4000000 INFO @ Wed, 22 Apr 2020 10:44:26: 5000000 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 Apr 2020 10:44:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.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 Apr 2020 10:44:30: #1 read tag files... INFO @ Wed, 22 Apr 2020 10:44:30: #1 read treatment tags... INFO @ Wed, 22 Apr 2020 10:44:31: 6000000 INFO @ Wed, 22 Apr 2020 10:44:36: 1000000 INFO @ Wed, 22 Apr 2020 10:44:36: 7000000 INFO @ Wed, 22 Apr 2020 10:44:41: 2000000 INFO @ Wed, 22 Apr 2020 10:44:42: 8000000 INFO @ Wed, 22 Apr 2020 10:44:46: 3000000 INFO @ Wed, 22 Apr 2020 10:44:47: 9000000 INFO @ Wed, 22 Apr 2020 10:44:52: #1 tag size is determined as 38 bps INFO @ Wed, 22 Apr 2020 10:44:52: #1 tag size = 38 INFO @ Wed, 22 Apr 2020 10:44:52: #1 total tags in treatment: 4932555 INFO @ Wed, 22 Apr 2020 10:44:52: #1 user defined the maximum tags... INFO @ Wed, 22 Apr 2020 10:44:52: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Apr 2020 10:44:52: 4000000 INFO @ Wed, 22 Apr 2020 10:44:52: #1 tags after filtering in treatment: 3957646 INFO @ Wed, 22 Apr 2020 10:44:52: #1 Redundant rate of treatment: 0.20 INFO @ Wed, 22 Apr 2020 10:44:52: #1 finished! INFO @ Wed, 22 Apr 2020 10:44:52: #2 Build Peak Model... INFO @ Wed, 22 Apr 2020 10:44:52: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Apr 2020 10:44:52: #2 number of paired peaks: 75 WARNING @ Wed, 22 Apr 2020 10:44:52: Too few paired peaks (75) 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 Apr 2020 10:44:52: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.10_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/SRX7741020/SRX7741020.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Wed, 22 Apr 2020 10:44:57: 5000000 INFO @ Wed, 22 Apr 2020 10:45:02: 6000000 INFO @ Wed, 22 Apr 2020 10:45:07: 7000000 INFO @ Wed, 22 Apr 2020 10:45:12: 8000000 INFO @ Wed, 22 Apr 2020 10:45:17: 9000000 INFO @ Wed, 22 Apr 2020 10:45:21: #1 tag size is determined as 38 bps INFO @ Wed, 22 Apr 2020 10:45:21: #1 tag size = 38 INFO @ Wed, 22 Apr 2020 10:45:21: #1 total tags in treatment: 4932555 INFO @ Wed, 22 Apr 2020 10:45:21: #1 user defined the maximum tags... INFO @ Wed, 22 Apr 2020 10:45:21: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Apr 2020 10:45:21: #1 tags after filtering in treatment: 3957646 INFO @ Wed, 22 Apr 2020 10:45:21: #1 Redundant rate of treatment: 0.20 INFO @ Wed, 22 Apr 2020 10:45:21: #1 finished! INFO @ Wed, 22 Apr 2020 10:45:21: #2 Build Peak Model... INFO @ Wed, 22 Apr 2020 10:45:21: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Apr 2020 10:45:21: #2 number of paired peaks: 75 WARNING @ Wed, 22 Apr 2020 10:45:21: Too few paired peaks (75) 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 Apr 2020 10:45:21: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.20_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/SRX7741020/SRX7741020.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7741020/SRX7741020.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。