Job ID = 2011021 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 9,587,629 reads read : 19,175,258 reads written : 9,587,629 reads 0-length : 9,587,629 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: 00:01:39 9587629 reads; of these: 9587629 (100.00%) were unpaired; of these: 577722 (6.03%) aligned 0 times 7592407 (79.19%) aligned exactly 1 time 1417500 (14.78%) aligned >1 times 93.97% overall alignment rate Time searching: 00:01:39 Overall time: 00:01:39 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] 3852122 / 9009907 = 0.4275 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 01:46:12: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.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 01:46:12: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:46:12: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:46:13: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.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 01:46:13: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:46:13: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:46:14: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.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 01:46:14: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:46:14: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:46:22: 1000000 INFO @ Sat, 06 Jul 2019 01:46:23: 1000000 INFO @ Sat, 06 Jul 2019 01:46:24: 1000000 INFO @ Sat, 06 Jul 2019 01:46:32: 2000000 INFO @ Sat, 06 Jul 2019 01:46:33: 2000000 INFO @ Sat, 06 Jul 2019 01:46:34: 2000000 INFO @ Sat, 06 Jul 2019 01:46:42: 3000000 INFO @ Sat, 06 Jul 2019 01:46:43: 3000000 INFO @ Sat, 06 Jul 2019 01:46:44: 3000000 INFO @ Sat, 06 Jul 2019 01:46:51: 4000000 INFO @ Sat, 06 Jul 2019 01:46:52: 4000000 INFO @ Sat, 06 Jul 2019 01:46:53: 4000000 INFO @ Sat, 06 Jul 2019 01:47:01: 5000000 INFO @ Sat, 06 Jul 2019 01:47:02: 5000000 INFO @ Sat, 06 Jul 2019 01:47:02: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 01:47:02: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 01:47:02: #1 total tags in treatment: 5157785 INFO @ Sat, 06 Jul 2019 01:47:02: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:47:02: #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 01:47:02: #1 tags after filtering in treatment: 5157785 INFO @ Sat, 06 Jul 2019 01:47:02: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:47:02: #1 finished! INFO @ Sat, 06 Jul 2019 01:47:02: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:47:02: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:47:03: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:47:03: Too few paired peaks (0) 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 01:47:03: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.05_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/SRX4550101/SRX4550101.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 01:47:03: 5000000 INFO @ Sat, 06 Jul 2019 01:47:03: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 01:47:03: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 01:47:03: #1 total tags in treatment: 5157785 INFO @ Sat, 06 Jul 2019 01:47:03: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:47:03: #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 01:47:03: #1 tags after filtering in treatment: 5157785 INFO @ Sat, 06 Jul 2019 01:47:03: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:47:03: #1 finished! INFO @ Sat, 06 Jul 2019 01:47:03: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:47:03: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:47:04: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:47:04: Too few paired peaks (0) 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 01:47:04: Process for pairing-model is terminated! INFO @ Sat, 06 Jul 2019 01:47:04: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 01:47:04: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 01:47:04: #1 total tags in treatment: 5157785 INFO @ Sat, 06 Jul 2019 01:47:04: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:47:04: #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 01:47:04: #1 tags after filtering in treatment: 5157785 INFO @ Sat, 06 Jul 2019 01:47:04: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:47:04: #1 finished! INFO @ Sat, 06 Jul 2019 01:47:04: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:47:04: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:47:05: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:47:05: Too few paired peaks (0) 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 01:47:05: Process for pairing-model is terminated! BedGraph に変換しました。 cut: /home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.10_peaks.narrowPeak: No such file or directory cut: /home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.20_peaks.narrowPeak: No such file or directory BigWig に変換中... pass1 - making usageList (0 chroms): 2 millis pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.10_peaks.narrowPeak’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550101/SRX4550101.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling CompletedMACS2peakCalling BigWig に変換しました。