Job ID = 2008002 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... spots read : 1,834,544 reads read : 3,669,088 reads written : 3,669,088 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 1834544 reads; of these: 1834544 (100.00%) were paired; of these: 268886 (14.66%) aligned concordantly 0 times 1430916 (78.00%) aligned concordantly exactly 1 time 134742 (7.34%) aligned concordantly >1 times ---- 268886 pairs aligned concordantly 0 times; of these: 159165 (59.19%) aligned discordantly 1 time ---- 109721 pairs aligned 0 times concordantly or discordantly; of these: 219442 mates make up the pairs; of these: 148612 (67.72%) aligned 0 times 35935 (16.38%) aligned exactly 1 time 34895 (15.90%) aligned >1 times 95.95% 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] 9580 / 1715941 = 0.0056 in library ' ' BAM に変換しました。 Bed ファイルを作成中... BedGraph に変換中... INFO @ Fri, 05 Jul 2019 17:09:19: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.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 @ Fri, 05 Jul 2019 17:09:19: #1 read tag files... INFO @ Fri, 05 Jul 2019 17:09:19: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 17:09:20: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.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 @ Fri, 05 Jul 2019 17:09:20: #1 read tag files... INFO @ Fri, 05 Jul 2019 17:09:20: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 17:09:21: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.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 @ Fri, 05 Jul 2019 17:09:21: #1 read tag files... INFO @ Fri, 05 Jul 2019 17:09:21: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 17:09:28: 1000000 INFO @ Fri, 05 Jul 2019 17:09:29: 1000000 INFO @ Fri, 05 Jul 2019 17:09:31: 1000000 INFO @ Fri, 05 Jul 2019 17:09:38: 2000000 INFO @ Fri, 05 Jul 2019 17:09:39: 2000000 INFO @ Fri, 05 Jul 2019 17:09:40: 2000000 INFO @ Fri, 05 Jul 2019 17:09:47: 3000000 INFO @ Fri, 05 Jul 2019 17:09:48: 3000000 INFO @ Fri, 05 Jul 2019 17:09:49: 3000000 INFO @ Fri, 05 Jul 2019 17:09:51: #1 tag size is determined as 100 bps INFO @ Fri, 05 Jul 2019 17:09:51: #1 tag size = 100 INFO @ Fri, 05 Jul 2019 17:09:51: #1 total tags in treatment: 1556508 INFO @ Fri, 05 Jul 2019 17:09:51: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 17:09:51: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 17:09:51: #1 tags after filtering in treatment: 1496632 INFO @ Fri, 05 Jul 2019 17:09:51: #1 Redundant rate of treatment: 0.04 INFO @ Fri, 05 Jul 2019 17:09:51: #1 finished! INFO @ Fri, 05 Jul 2019 17:09:51: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 17:09:51: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 17:09:51: #2 number of paired peaks: 21 WARNING @ Fri, 05 Jul 2019 17:09:51: Too few paired peaks (21) 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 @ Fri, 05 Jul 2019 17:09:51: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.05_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/ERX471791/ERX471791.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 17:09:52: #1 tag size is determined as 100 bps INFO @ Fri, 05 Jul 2019 17:09:52: #1 tag size = 100 INFO @ Fri, 05 Jul 2019 17:09:52: #1 total tags in treatment: 1556508 INFO @ Fri, 05 Jul 2019 17:09:52: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 17:09:52: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 17:09:52: #1 tags after filtering in treatment: 1496632 INFO @ Fri, 05 Jul 2019 17:09:52: #1 Redundant rate of treatment: 0.04 INFO @ Fri, 05 Jul 2019 17:09:52: #1 finished! INFO @ Fri, 05 Jul 2019 17:09:52: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 17:09:52: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 17:09:52: #2 number of paired peaks: 21 WARNING @ Fri, 05 Jul 2019 17:09:52: Too few paired peaks (21) 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 @ Fri, 05 Jul 2019 17:09:52: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.10_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/ERX471791/ERX471791.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 17:09:54: #1 tag size is determined as 100 bps INFO @ Fri, 05 Jul 2019 17:09:54: #1 tag size = 100 INFO @ Fri, 05 Jul 2019 17:09:54: #1 total tags in treatment: 1556508 INFO @ Fri, 05 Jul 2019 17:09:54: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 17:09:54: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 17:09:54: #1 tags after filtering in treatment: 1496632 INFO @ Fri, 05 Jul 2019 17:09:54: #1 Redundant rate of treatment: 0.04 INFO @ Fri, 05 Jul 2019 17:09:54: #1 finished! INFO @ Fri, 05 Jul 2019 17:09:54: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 17:09:54: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 17:09:54: #2 number of paired peaks: 21 WARNING @ Fri, 05 Jul 2019 17:09:54: Too few paired peaks (21) 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 @ Fri, 05 Jul 2019 17:09:54: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.20_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/ERX471791/ERX471791.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX471791/ERX471791.20_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。