Job ID = 2008186 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... spots read : 9,671,545 reads read : 19,343,090 reads written : 19,343,090 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/ERR629011.sra.cache’: 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: 00:00:01 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:06:03 9671545 reads; of these: 9671545 (100.00%) were paired; of these: 780837 (8.07%) aligned concordantly 0 times 8517527 (88.07%) aligned concordantly exactly 1 time 373181 (3.86%) aligned concordantly >1 times ---- 780837 pairs aligned concordantly 0 times; of these: 60742 (7.78%) aligned discordantly 1 time ---- 720095 pairs aligned 0 times concordantly or discordantly; of these: 1440190 mates make up the pairs; of these: 1403702 (97.47%) aligned 0 times 27832 (1.93%) aligned exactly 1 time 8656 (0.60%) aligned >1 times 92.74% overall alignment rate Time searching: 00:06:04 Overall time: 00:06:04 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] 7957375 / 8945503 = 0.8895 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 17:46:31: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.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 17:46:31: #1 read tag files... INFO @ Fri, 05 Jul 2019 17:46:31: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 17:46:32: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.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 17:46:32: #1 read tag files... INFO @ Fri, 05 Jul 2019 17:46:32: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 17:46:33: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.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 17:46:33: #1 read tag files... INFO @ Fri, 05 Jul 2019 17:46:33: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 17:46:38: 1000000 INFO @ Fri, 05 Jul 2019 17:46:38: 1000000 INFO @ Fri, 05 Jul 2019 17:46:41: 1000000 INFO @ Fri, 05 Jul 2019 17:46:44: 2000000 INFO @ Fri, 05 Jul 2019 17:46:44: #1 tag size is determined as 44 bps INFO @ Fri, 05 Jul 2019 17:46:44: #1 tag size = 44 INFO @ Fri, 05 Jul 2019 17:46:44: #1 total tags in treatment: 948414 INFO @ Fri, 05 Jul 2019 17:46:44: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 17:46:44: #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 17:46:44: #1 tags after filtering in treatment: 707548 INFO @ Fri, 05 Jul 2019 17:46:44: #1 Redundant rate of treatment: 0.25 INFO @ Fri, 05 Jul 2019 17:46:44: #1 finished! INFO @ Fri, 05 Jul 2019 17:46:44: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 17:46:44: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 17:46:44: #2 number of paired peaks: 60 WARNING @ Fri, 05 Jul 2019 17:46:44: Too few paired peaks (60) 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 17:46:44: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.05_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 17:46:45: 2000000 INFO @ Fri, 05 Jul 2019 17:46:45: #1 tag size is determined as 44 bps INFO @ Fri, 05 Jul 2019 17:46:45: #1 tag size = 44 INFO @ Fri, 05 Jul 2019 17:46:45: #1 total tags in treatment: 948414 INFO @ Fri, 05 Jul 2019 17:46:45: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 17:46:45: #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 17:46:45: #1 tags after filtering in treatment: 707548 INFO @ Fri, 05 Jul 2019 17:46:45: #1 Redundant rate of treatment: 0.25 INFO @ Fri, 05 Jul 2019 17:46:45: #1 finished! INFO @ Fri, 05 Jul 2019 17:46:45: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 17:46:45: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 17:46:45: #2 number of paired peaks: 60 WARNING @ Fri, 05 Jul 2019 17:46:45: Too few paired peaks (60) 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 17:46:45: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.10_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/ERX585721/ERX585721.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 17:46:48: 2000000 INFO @ Fri, 05 Jul 2019 17:46:48: #1 tag size is determined as 44 bps INFO @ Fri, 05 Jul 2019 17:46:48: #1 tag size = 44 INFO @ Fri, 05 Jul 2019 17:46:48: #1 total tags in treatment: 948414 INFO @ Fri, 05 Jul 2019 17:46:48: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 17:46:48: #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 17:46:48: #1 tags after filtering in treatment: 707548 INFO @ Fri, 05 Jul 2019 17:46:48: #1 Redundant rate of treatment: 0.25 INFO @ Fri, 05 Jul 2019 17:46:48: #1 finished! INFO @ Fri, 05 Jul 2019 17:46:48: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 17:46:48: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 17:46:48: #2 number of paired peaks: 60 WARNING @ Fri, 05 Jul 2019 17:46:48: Too few paired peaks (60) 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 17:46:48: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.20_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/ERX585721/ERX585721.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX585721/ERX585721.20_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。