Job ID = 2007863 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... spots read : 215,731 reads read : 431,462 reads written : 431,462 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: 00:00:07 215731 reads; of these: 215731 (100.00%) were paired; of these: 36341 (16.85%) aligned concordantly 0 times 164445 (76.23%) aligned concordantly exactly 1 time 14945 (6.93%) aligned concordantly >1 times ---- 36341 pairs aligned concordantly 0 times; of these: 23217 (63.89%) aligned discordantly 1 time ---- 13124 pairs aligned 0 times concordantly or discordantly; of these: 26248 mates make up the pairs; of these: 17906 (68.22%) aligned 0 times 3627 (13.82%) aligned exactly 1 time 4715 (17.96%) aligned >1 times 95.85% overall alignment rate Time searching: 00:00:07 Overall time: 00:00:07 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] 226 / 200091 = 0.0011 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 16:36:21: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.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 16:36:21: #1 read tag files... INFO @ Fri, 05 Jul 2019 16:36:21: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 16:36:22: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.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 16:36:22: #1 read tag files... INFO @ Fri, 05 Jul 2019 16:36:22: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 16:36:23: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.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 16:36:23: #1 read tag files... INFO @ Fri, 05 Jul 2019 16:36:23: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 16:36:25: #1 tag size is determined as 25 bps INFO @ Fri, 05 Jul 2019 16:36:25: #1 tag size = 25 INFO @ Fri, 05 Jul 2019 16:36:25: #1 total tags in treatment: 179191 INFO @ Fri, 05 Jul 2019 16:36:25: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 16:36:25: #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 16:36:25: #1 tags after filtering in treatment: 178388 INFO @ Fri, 05 Jul 2019 16:36:25: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 16:36:25: #1 finished! INFO @ Fri, 05 Jul 2019 16:36:25: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 16:36:25: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 16:36:25: #2 number of paired peaks: 21 WARNING @ Fri, 05 Jul 2019 16:36:25: 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 16:36:25: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.05_peaks.narrowPeakINFO @ Fri, 05 Jul 2019 16:36:25: #1 tag size is determined as 25 bps : No such file or directory INFO @ Fri, 05 Jul 2019 16:36:26: #1 tag size = 25 INFO @ Fri, 05 Jul 2019 16:36:26: #1 total tags in treatment: 179191 INFO @ Fri, 05 Jul 2019 16:36:26: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 16:36:26: #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 16:36:26: #1 tags after filtering in treatment: 178388 INFO @ Fri, 05 Jul 2019 16:36:26: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 16:36:26: #1 finished! INFO @ Fri, 05 Jul 2019 16:36:26: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 16:36:26: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 16:36:26: #2 number of paired peaks: 21 WARNING @ Fri, 05 Jul 2019 16:36:26: 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 16:36:26: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.10_peaks.narrowPeak: No such file or directory INFO @ Fri, 05 Jul 2019 16:36:27: #1 tag size is determined as 25 bps INFO @ Fri, 05 Jul 2019 16:36:27: #1 tag size = 25 INFO @ Fri, 05 Jul 2019 16:36:27: #1 total tags in treatment: 179191 INFO @ Fri, 05 Jul 2019 16:36:27: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 16:36:27: #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 16:36:27: #1 tags after filtering in treatment: 178388 INFO @ Fri, 05 Jul 2019 16:36:27: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 16:36:27: #1 finished! INFO @ Fri, 05 Jul 2019 16:36:27: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 16:36:27: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 16:36:27: #2 number of paired peaks: 21 WARNING @ Fri, 05 Jul 2019 16:36:27: 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 16:36:27: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.20_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 901 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling pass1 - making usageList (0 chroms): 308 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX462403/ERX462403.10_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。