Job ID = 2008073 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... spots read : 1,818,507 reads read : 3,637,014 reads written : 3,637,014 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: 00:01:55 1818507 reads; of these: 1818507 (100.00%) were paired; of these: 283902 (15.61%) aligned concordantly 0 times 1436487 (78.99%) aligned concordantly exactly 1 time 98118 (5.40%) aligned concordantly >1 times ---- 283902 pairs aligned concordantly 0 times; of these: 125139 (44.08%) aligned discordantly 1 time ---- 158763 pairs aligned 0 times concordantly or discordantly; of these: 317526 mates make up the pairs; of these: 265671 (83.67%) aligned 0 times 30514 (9.61%) aligned exactly 1 time 21341 (6.72%) aligned >1 times 92.70% overall alignment rate Time searching: 00:01:56 Overall time: 00:01:56 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] 85336 / 1651035 = 0.0517 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 17:31:58: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.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 17:31:58: #1 read tag files... INFO @ Fri, 05 Jul 2019 17:31:58: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 17:31:59: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.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 17:31:59: #1 read tag files... INFO @ Fri, 05 Jul 2019 17:31:59: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 17:32:00: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.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 17:32:00: #1 read tag files... INFO @ Fri, 05 Jul 2019 17:32:00: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 17:32:07: 1000000 INFO @ Fri, 05 Jul 2019 17:32:10: 1000000 INFO @ Fri, 05 Jul 2019 17:32:13: 1000000 INFO @ Fri, 05 Jul 2019 17:32:16: 2000000 INFO @ Fri, 05 Jul 2019 17:32:21: 2000000 INFO @ Fri, 05 Jul 2019 17:32:26: 3000000 INFO @ Fri, 05 Jul 2019 17:32:27: 2000000 INFO @ Fri, 05 Jul 2019 17:32:27: #1 tag size is determined as 100 bps INFO @ Fri, 05 Jul 2019 17:32:27: #1 tag size = 100 INFO @ Fri, 05 Jul 2019 17:32:27: #1 total tags in treatment: 1452754 INFO @ Fri, 05 Jul 2019 17:32:27: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 17:32:27: #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 17:32:27: #1 tags after filtering in treatment: 1360827 INFO @ Fri, 05 Jul 2019 17:32:27: #1 Redundant rate of treatment: 0.06 INFO @ Fri, 05 Jul 2019 17:32:27: #1 finished! INFO @ Fri, 05 Jul 2019 17:32:27: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 17:32:27: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 17:32:28: #2 number of paired peaks: 21 WARNING @ Fri, 05 Jul 2019 17:32:28: 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 17:32:28: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.05_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/ERX471854/ERX471854.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 17:32:32: 3000000 INFO @ Fri, 05 Jul 2019 17:32:34: #1 tag size is determined as 100 bps INFO @ Fri, 05 Jul 2019 17:32:34: #1 tag size = 100 INFO @ Fri, 05 Jul 2019 17:32:34: #1 total tags in treatment: 1452754 INFO @ Fri, 05 Jul 2019 17:32:34: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 17:32:34: #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 17:32:34: #1 tags after filtering in treatment: 1360827 INFO @ Fri, 05 Jul 2019 17:32:34: #1 Redundant rate of treatment: 0.06 INFO @ Fri, 05 Jul 2019 17:32:34: #1 finished! INFO @ Fri, 05 Jul 2019 17:32:34: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 17:32:34: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 17:32:34: #2 number of paired peaks: 21 WARNING @ Fri, 05 Jul 2019 17:32:34: 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 17:32:34: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.10_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/ERX471854/ERX471854.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 17:32:40: 3000000 INFO @ Fri, 05 Jul 2019 17:32:42: #1 tag size is determined as 100 bps INFO @ Fri, 05 Jul 2019 17:32:42: #1 tag size = 100 INFO @ Fri, 05 Jul 2019 17:32:42: #1 total tags in treatment: 1452754 INFO @ Fri, 05 Jul 2019 17:32:42: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 17:32:42: #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 17:32:42: #1 tags after filtering in treatment: 1360827 INFO @ Fri, 05 Jul 2019 17:32:42: #1 Redundant rate of treatment: 0.06 INFO @ Fri, 05 Jul 2019 17:32:42: #1 finished! INFO @ Fri, 05 Jul 2019 17:32:42: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 17:32:42: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 17:32:42: #2 number of paired peaks: 21 WARNING @ Fri, 05 Jul 2019 17:32:42: 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 17:32:42: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.20_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/ERX471854/ERX471854.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX471854/ERX471854.20_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。