Job ID = 4289315 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2019-12-10T05:07:55 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 : 23,493,049 reads read : 23,493,049 reads written : 23,493,049 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: 00:04:07 23493049 reads; of these: 23493049 (100.00%) were unpaired; of these: 1027804 (4.37%) aligned 0 times 19829469 (84.41%) aligned exactly 1 time 2635776 (11.22%) aligned >1 times 95.63% overall alignment rate Time searching: 00:04:07 Overall time: 00:04:07 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_sort_core] merging from 12 files... [bam_rmdupse_core] 11338818 / 22465245 = 0.5047 in library ' ' BAM に変換しました。 Bed ファイルを作成中... INFO @ Tue, 10 Dec 2019 14:18:54: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.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 @ Tue, 10 Dec 2019 14:18:54: #1 read tag files... INFO @ Tue, 10 Dec 2019 14:18:54: #1 read treatment tags... INFO @ Tue, 10 Dec 2019 14:19:01: 1000000 INFO @ Tue, 10 Dec 2019 14:19:08: 2000000 INFO @ Tue, 10 Dec 2019 14:19:15: 3000000 INFO @ Tue, 10 Dec 2019 14:19:22: 4000000 INFO @ Tue, 10 Dec 2019 14:19:24: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.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 @ Tue, 10 Dec 2019 14:19:24: #1 read tag files... INFO @ Tue, 10 Dec 2019 14:19:24: #1 read treatment tags... INFO @ Tue, 10 Dec 2019 14:19:30: 5000000 INFO @ Tue, 10 Dec 2019 14:19:31: 1000000 INFO @ Tue, 10 Dec 2019 14:19:37: 6000000 INFO @ Tue, 10 Dec 2019 14:19:39: 2000000 INFO @ Tue, 10 Dec 2019 14:19:44: 7000000 INFO @ Tue, 10 Dec 2019 14:19:47: 3000000 INFO @ Tue, 10 Dec 2019 14:19:51: 8000000 BedGraph に変換中... INFO @ Tue, 10 Dec 2019 14:19:54: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.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 @ Tue, 10 Dec 2019 14:19:54: #1 read tag files... INFO @ Tue, 10 Dec 2019 14:19:54: #1 read treatment tags... INFO @ Tue, 10 Dec 2019 14:19:54: 4000000 INFO @ Tue, 10 Dec 2019 14:19:58: 9000000 INFO @ Tue, 10 Dec 2019 14:20:00: 1000000 INFO @ Tue, 10 Dec 2019 14:20:02: 5000000 INFO @ Tue, 10 Dec 2019 14:20:05: 10000000 INFO @ Tue, 10 Dec 2019 14:20:07: 2000000 INFO @ Tue, 10 Dec 2019 14:20:10: 6000000 INFO @ Tue, 10 Dec 2019 14:20:12: 11000000 INFO @ Tue, 10 Dec 2019 14:20:13: #1 tag size is determined as 51 bps INFO @ Tue, 10 Dec 2019 14:20:13: #1 tag size = 51 INFO @ Tue, 10 Dec 2019 14:20:13: #1 total tags in treatment: 11126427 INFO @ Tue, 10 Dec 2019 14:20:13: #1 user defined the maximum tags... INFO @ Tue, 10 Dec 2019 14:20:13: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 10 Dec 2019 14:20:13: 3000000 INFO @ Tue, 10 Dec 2019 14:20:13: #1 tags after filtering in treatment: 11126427 INFO @ Tue, 10 Dec 2019 14:20:13: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 10 Dec 2019 14:20:13: #1 finished! INFO @ Tue, 10 Dec 2019 14:20:13: #2 Build Peak Model... INFO @ Tue, 10 Dec 2019 14:20:13: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 10 Dec 2019 14:20:14: #2 number of paired peaks: 0 WARNING @ Tue, 10 Dec 2019 14:20:14: 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 @ Tue, 10 Dec 2019 14:20:14: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.05_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/SRX6678235/SRX6678235.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Tue, 10 Dec 2019 14:20:17: 7000000 INFO @ Tue, 10 Dec 2019 14:20:19: 4000000 INFO @ Tue, 10 Dec 2019 14:20:25: 8000000 INFO @ Tue, 10 Dec 2019 14:20:26: 5000000 INFO @ Tue, 10 Dec 2019 14:20:32: 6000000 INFO @ Tue, 10 Dec 2019 14:20:33: 9000000 INFO @ Tue, 10 Dec 2019 14:20:39: 7000000 INFO @ Tue, 10 Dec 2019 14:20:40: 10000000 INFO @ Tue, 10 Dec 2019 14:20:45: 8000000 INFO @ Tue, 10 Dec 2019 14:20:48: 11000000 INFO @ Tue, 10 Dec 2019 14:20:49: #1 tag size is determined as 51 bps INFO @ Tue, 10 Dec 2019 14:20:49: #1 tag size = 51 INFO @ Tue, 10 Dec 2019 14:20:49: #1 total tags in treatment: 11126427 INFO @ Tue, 10 Dec 2019 14:20:49: #1 user defined the maximum tags... INFO @ Tue, 10 Dec 2019 14:20:49: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 10 Dec 2019 14:20:49: #1 tags after filtering in treatment: 11126427 INFO @ Tue, 10 Dec 2019 14:20:49: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 10 Dec 2019 14:20:49: #1 finished! INFO @ Tue, 10 Dec 2019 14:20:49: #2 Build Peak Model... INFO @ Tue, 10 Dec 2019 14:20:49: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 10 Dec 2019 14:20:50: #2 number of paired peaks: 0 WARNING @ Tue, 10 Dec 2019 14:20:50: 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 @ Tue, 10 Dec 2019 14:20:50: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.10_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/SRX6678235/SRX6678235.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Tue, 10 Dec 2019 14:20:51: 9000000 INFO @ Tue, 10 Dec 2019 14:20:58: 10000000 INFO @ Tue, 10 Dec 2019 14:21:04: 11000000 INFO @ Tue, 10 Dec 2019 14:21:05: #1 tag size is determined as 51 bps INFO @ Tue, 10 Dec 2019 14:21:05: #1 tag size = 51 INFO @ Tue, 10 Dec 2019 14:21:05: #1 total tags in treatment: 11126427 INFO @ Tue, 10 Dec 2019 14:21:05: #1 user defined the maximum tags... INFO @ Tue, 10 Dec 2019 14:21:05: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 10 Dec 2019 14:21:05: #1 tags after filtering in treatment: 11126427 INFO @ Tue, 10 Dec 2019 14:21:05: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 10 Dec 2019 14:21:05: #1 finished! INFO @ Tue, 10 Dec 2019 14:21:05: #2 Build Peak Model... INFO @ Tue, 10 Dec 2019 14:21:05: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 10 Dec 2019 14:21:06: #2 number of paired peaks: 0 WARNING @ Tue, 10 Dec 2019 14:21:06: 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 @ Tue, 10 Dec 2019 14:21:06: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.20_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/SRX6678235/SRX6678235.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6678235/SRX6678235.20_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。