Job ID = 2009880 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2019-07-05T11:22:19 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 : 11,353,344 reads read : 11,353,344 reads written : 11,353,344 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: 00:01:53 11353344 reads; of these: 11353344 (100.00%) were unpaired; of these: 558999 (4.92%) aligned 0 times 8788418 (77.41%) aligned exactly 1 time 2005927 (17.67%) aligned >1 times 95.08% overall alignment rate Time searching: 00:01:53 Overall time: 00:01:53 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 8 files... [bam_rmdupse_core] 5311063 / 10794345 = 0.4920 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 20:30:16: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.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 20:30:16: #1 read tag files... INFO @ Fri, 05 Jul 2019 20:30:16: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 20:30:17: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.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 20:30:17: #1 read tag files... INFO @ Fri, 05 Jul 2019 20:30:17: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 20:30:18: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.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 20:30:18: #1 read tag files... INFO @ Fri, 05 Jul 2019 20:30:18: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 20:30:25: 1000000 INFO @ Fri, 05 Jul 2019 20:30:25: 1000000 INFO @ Fri, 05 Jul 2019 20:30:27: 1000000 INFO @ Fri, 05 Jul 2019 20:30:33: 2000000 INFO @ Fri, 05 Jul 2019 20:30:34: 2000000 INFO @ Fri, 05 Jul 2019 20:30:37: 2000000 INFO @ Fri, 05 Jul 2019 20:30:41: 3000000 INFO @ Fri, 05 Jul 2019 20:30:43: 3000000 INFO @ Fri, 05 Jul 2019 20:30:46: 3000000 INFO @ Fri, 05 Jul 2019 20:30:49: 4000000 INFO @ Fri, 05 Jul 2019 20:30:51: 4000000 INFO @ Fri, 05 Jul 2019 20:30:55: 4000000 INFO @ Fri, 05 Jul 2019 20:30:57: 5000000 INFO @ Fri, 05 Jul 2019 20:31:00: 5000000 INFO @ Fri, 05 Jul 2019 20:31:00: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 20:31:00: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 20:31:00: #1 total tags in treatment: 5483282 INFO @ Fri, 05 Jul 2019 20:31:00: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:31:00: #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 20:31:00: #1 tags after filtering in treatment: 5483282 INFO @ Fri, 05 Jul 2019 20:31:00: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:31:00: #1 finished! INFO @ Fri, 05 Jul 2019 20:31:00: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:31:00: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:31:01: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:31:01: 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 20:31:01: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.10_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 1324 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 20:31:04: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 20:31:04: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 20:31:04: #1 total tags in treatment: 5483282 INFO @ Fri, 05 Jul 2019 20:31:04: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:31:04: #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 20:31:04: 5000000 INFO @ Fri, 05 Jul 2019 20:31:04: #1 tags after filtering in treatment: 5483282 INFO @ Fri, 05 Jul 2019 20:31:04: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:31:04: #1 finished! INFO @ Fri, 05 Jul 2019 20:31:04: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:31:04: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:31:04: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:31:04: 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 @ Fri, 05 Jul 2019 20:31:04: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.05_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/SRX2148731/SRX2148731.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 20:31:08: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 20:31:08: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 20:31:08: #1 total tags in treatment: 5483282 INFO @ Fri, 05 Jul 2019 20:31:08: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:31:08: #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 20:31:08: #1 tags after filtering in treatment: 5483282 INFO @ Fri, 05 Jul 2019 20:31:08: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:31:08: #1 finished! INFO @ Fri, 05 Jul 2019 20:31:08: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:31:08: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:31:08: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:31:08: 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 20:31:08: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.20_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/SRX2148731/SRX2148731.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148731/SRX2148731.20_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。