Job ID = 2010117 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2019-07-05T12:21:28 fasterq-dump.2.9.6 sys: timeout exhausted while reading file within network system module - mbedtls_ssl_read returned -76 ( NET - Reading information from the socket failed ) spots read : 10,920,752 reads read : 10,920,752 reads written : 10,920,752 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: 00:01:36 10920752 reads; of these: 10920752 (100.00%) were unpaired; of these: 3656252 (33.48%) aligned 0 times 6440337 (58.97%) aligned exactly 1 time 824163 (7.55%) aligned >1 times 66.52% overall alignment rate Time searching: 00:01:36 Overall time: 00:01:36 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] 1979022 / 7264500 = 0.2724 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 21:26:21: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.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 21:26:21: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:26:21: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:26:22: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.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 21:26:22: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:26:22: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:26:23: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.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 21:26:23: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:26:23: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:26:30: 1000000 INFO @ Fri, 05 Jul 2019 21:26:30: 1000000 INFO @ Fri, 05 Jul 2019 21:26:32: 1000000 INFO @ Fri, 05 Jul 2019 21:26:37: 2000000 INFO @ Fri, 05 Jul 2019 21:26:38: 2000000 INFO @ Fri, 05 Jul 2019 21:26:40: 2000000 INFO @ Fri, 05 Jul 2019 21:26:45: 3000000 INFO @ Fri, 05 Jul 2019 21:26:46: 3000000 INFO @ Fri, 05 Jul 2019 21:26:48: 3000000 INFO @ Fri, 05 Jul 2019 21:26:52: 4000000 INFO @ Fri, 05 Jul 2019 21:26:54: 4000000 INFO @ Fri, 05 Jul 2019 21:26:55: 4000000 INFO @ Fri, 05 Jul 2019 21:26:59: 5000000 INFO @ Fri, 05 Jul 2019 21:27:01: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:27:01: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:27:01: #1 total tags in treatment: 5285478 INFO @ Fri, 05 Jul 2019 21:27:01: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:27:01: #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 21:27:01: #1 tags after filtering in treatment: 5285478 INFO @ Fri, 05 Jul 2019 21:27:01: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:27:01: #1 finished! INFO @ Fri, 05 Jul 2019 21:27:01: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:27:01: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:27:01: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:27:01: 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 @ Fri, 05 Jul 2019 21:27:01: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.10_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/SRX2772195/SRX2772195.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 21:27:02: 5000000 INFO @ Fri, 05 Jul 2019 21:27:03: 5000000 INFO @ Fri, 05 Jul 2019 21:27:04: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:27:04: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:27:04: #1 total tags in treatment: 5285478 INFO @ Fri, 05 Jul 2019 21:27:04: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:27:04: #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 21:27:05: #1 tags after filtering in treatment: 5285478 INFO @ Fri, 05 Jul 2019 21:27:05: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:27:05: #1 finished! INFO @ Fri, 05 Jul 2019 21:27:05: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:27:05: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:27:05: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:27:05: 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 @ Fri, 05 Jul 2019 21:27:05: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.05_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/SRX2772195/SRX2772195.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 21:27:05: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:27:05: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:27:05: #1 total tags in treatment: 5285478 INFO @ Fri, 05 Jul 2019 21:27:05: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:27:05: #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 21:27:05: #1 tags after filtering in treatment: 5285478 INFO @ Fri, 05 Jul 2019 21:27:05: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:27:05: #1 finished! INFO @ Fri, 05 Jul 2019 21:27:05: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:27:05: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:27:06: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:27:06: 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 @ Fri, 05 Jul 2019 21:27:06: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.20_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/SRX2772195/SRX2772195.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772195/SRX2772195.20_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。