Job ID = 2004159 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... spots read : 7,661,400 reads read : 15,322,800 reads written : 15,322,800 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: 00:01:32 7661400 reads; of these: 7661400 (100.00%) were paired; of these: 7300316 (95.29%) aligned concordantly 0 times 301186 (3.93%) aligned concordantly exactly 1 time 59898 (0.78%) aligned concordantly >1 times ---- 7300316 pairs aligned concordantly 0 times; of these: 79473 (1.09%) aligned discordantly 1 time ---- 7220843 pairs aligned 0 times concordantly or discordantly; of these: 14441686 mates make up the pairs; of these: 13784830 (95.45%) aligned 0 times 552787 (3.83%) aligned exactly 1 time 104069 (0.72%) aligned >1 times 10.04% overall alignment rate Time searching: 00:01:32 Overall time: 00:01:32 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] 96215 / 436768 = 0.2203 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 14:30:45: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.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 14:30:45: #1 read tag files... INFO @ Fri, 05 Jul 2019 14:30:45: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 14:30:46: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.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 14:30:46: #1 read tag files... INFO @ Fri, 05 Jul 2019 14:30:46: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 14:30:47: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.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 14:30:47: #1 read tag files... INFO @ Fri, 05 Jul 2019 14:30:47: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 14:30:51: 1000000 INFO @ Fri, 05 Jul 2019 14:30:54: #1 tag size is determined as 39 bps INFO @ Fri, 05 Jul 2019 14:30:54: #1 tag size = 39 INFO @ Fri, 05 Jul 2019 14:30:54: #1 total tags in treatment: 279880 INFO @ Fri, 05 Jul 2019 14:30:54: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 14:30:54: #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 14:30:54: #1 tags after filtering in treatment: 266131 INFO @ Fri, 05 Jul 2019 14:30:54: #1 Redundant rate of treatment: 0.05 INFO @ Fri, 05 Jul 2019 14:30:54: #1 finished! INFO @ Fri, 05 Jul 2019 14:30:54: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 14:30:54: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 14:30:54: #2 number of paired peaks: 64 WARNING @ Fri, 05 Jul 2019 14:30:54: Too few paired peaks (64) 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 14:30:54: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.05_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/ERX2070724/ERX2070724.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 14:30:54: 1000000 INFO @ Fri, 05 Jul 2019 14:30:55: 1000000 INFO @ Fri, 05 Jul 2019 14:30:57: #1 tag size is determined as 39 bps INFO @ Fri, 05 Jul 2019 14:30:57: #1 tag size = 39 INFO @ Fri, 05 Jul 2019 14:30:57: #1 total tags in treatment: 279880 INFO @ Fri, 05 Jul 2019 14:30:57: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 14:30:57: #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 14:30:57: #1 tags after filtering in treatment: 266131 INFO @ Fri, 05 Jul 2019 14:30:57: #1 Redundant rate of treatment: 0.05 INFO @ Fri, 05 Jul 2019 14:30:57: #1 finished! INFO @ Fri, 05 Jul 2019 14:30:57: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 14:30:57: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 14:30:57: #2 number of paired peaks: 64 WARNING @ Fri, 05 Jul 2019 14:30:57: Too few paired peaks (64) 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 14:30:57: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.20_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/ERX2070724/ERX2070724.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 14:30:58: #1 tag size is determined as 39 bps INFO @ Fri, 05 Jul 2019 14:30:58: #1 tag size = 39 INFO @ Fri, 05 Jul 2019 14:30:58: #1 total tags in treatment: 279880 INFO @ Fri, 05 Jul 2019 14:30:58: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 14:30:58: #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 14:30:58: #1 tags after filtering in treatment: 266131 INFO @ Fri, 05 Jul 2019 14:30:58: #1 Redundant rate of treatment: 0.05 INFO @ Fri, 05 Jul 2019 14:30:58: #1 finished! INFO @ Fri, 05 Jul 2019 14:30:58: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 14:30:58: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 14:30:58: #2 number of paired peaks: 64 WARNING @ Fri, 05 Jul 2019 14:30:58: Too few paired peaks (64) 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 14:30:58: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.10_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 241 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX2070724/ERX2070724.10_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。