Job ID = 2011019 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 7,999,388 reads read : 15,998,776 reads written : 7,999,388 reads 0-length : 7,999,388 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: 00:01:22 7999388 reads; of these: 7999388 (100.00%) were unpaired; of these: 441262 (5.52%) aligned 0 times 6302988 (78.79%) aligned exactly 1 time 1255138 (15.69%) aligned >1 times 94.48% overall alignment rate Time searching: 00:01:22 Overall time: 00:01:22 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_rmdupse_core] 3169169 / 7558126 = 0.4193 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 @ Sat, 06 Jul 2019 01:44:27: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.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 @ Sat, 06 Jul 2019 01:44:27: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:44:27: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:44:28: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.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 @ Sat, 06 Jul 2019 01:44:28: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:44:28: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:44:36: 1000000 INFO @ Sat, 06 Jul 2019 01:44:37: 1000000 INFO @ Sat, 06 Jul 2019 01:44:45: 2000000 INFO @ Sat, 06 Jul 2019 01:44:47: 2000000 INFO @ Sat, 06 Jul 2019 01:44:50: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.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 @ Sat, 06 Jul 2019 01:44:50: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:44:50: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:44:53: 3000000 INFO @ Sat, 06 Jul 2019 01:44:56: 3000000 INFO @ Sat, 06 Jul 2019 01:45:00: 1000000 INFO @ Sat, 06 Jul 2019 01:45:01: 4000000 INFO @ Sat, 06 Jul 2019 01:45:05: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 01:45:05: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 01:45:05: #1 total tags in treatment: 4388957 INFO @ Sat, 06 Jul 2019 01:45:05: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:45:05: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 06 Jul 2019 01:45:05: #1 tags after filtering in treatment: 4388957 INFO @ Sat, 06 Jul 2019 01:45:05: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:45:05: #1 finished! INFO @ Sat, 06 Jul 2019 01:45:05: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:45:05: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:45:05: #2 number of paired peaks: 29 WARNING @ Sat, 06 Jul 2019 01:45:05: Too few paired peaks (29) 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 @ Sat, 06 Jul 2019 01:45:05: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.10_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/SRX4550099/SRX4550099.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 01:45:06: 4000000 INFO @ Sat, 06 Jul 2019 01:45:09: 2000000 INFO @ Sat, 06 Jul 2019 01:45:10: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 01:45:10: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 01:45:10: #1 total tags in treatment: 4388957 INFO @ Sat, 06 Jul 2019 01:45:10: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:45:10: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 06 Jul 2019 01:45:10: #1 tags after filtering in treatment: 4388957 INFO @ Sat, 06 Jul 2019 01:45:10: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:45:10: #1 finished! INFO @ Sat, 06 Jul 2019 01:45:10: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:45:10: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:45:10: #2 number of paired peaks: 29 WARNING @ Sat, 06 Jul 2019 01:45:10: Too few paired peaks (29) 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 @ Sat, 06 Jul 2019 01:45:10: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.05_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/SRX4550099/SRX4550099.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 01:45:19: 3000000 INFO @ Sat, 06 Jul 2019 01:45:28: 4000000 INFO @ Sat, 06 Jul 2019 01:45:31: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 01:45:31: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 01:45:31: #1 total tags in treatment: 4388957 INFO @ Sat, 06 Jul 2019 01:45:31: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:45:31: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 06 Jul 2019 01:45:31: #1 tags after filtering in treatment: 4388957 INFO @ Sat, 06 Jul 2019 01:45:31: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:45:31: #1 finished! INFO @ Sat, 06 Jul 2019 01:45:31: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:45:31: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:45:32: #2 number of paired peaks: 29 WARNING @ Sat, 06 Jul 2019 01:45:32: Too few paired peaks (29) 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 @ Sat, 06 Jul 2019 01:45:32: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.20_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/SRX4550099/SRX4550099.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550099/SRX4550099.20_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。