Job ID = 2009644 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 116,394 reads read : 116,394 reads written : 116,394 spots read : 4,000,000 reads read : 4,000,000 reads written : 4,000,000 spots read : 4,000,000 reads read : 4,000,000 reads written : 4,000,000 spots read : 4,000,000 reads read : 4,000,000 reads written : 4,000,000 2019-07-05T10:26:19 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 ) 2019-07-05T10:26:19 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 : 4,000,000 reads read : 4,000,000 reads written : 4,000,000 rm: cannot remove ‘/home/okishinya/ncbi/public/sra/ERR778594.sra.cache’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/ERR778607.sra.cache’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/ERR778622.sra.cache’: 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: 00:03:15 16116394 reads; of these: 16116394 (100.00%) were unpaired; of these: 2386490 (14.81%) aligned 0 times 12981797 (80.55%) aligned exactly 1 time 748107 (4.64%) aligned >1 times 85.19% overall alignment rate Time searching: 00:03:15 Overall time: 00:03:15 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] 8788494 / 13729904 = 0.6401 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 19:35:08: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.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 19:35:08: #1 read tag files... INFO @ Fri, 05 Jul 2019 19:35:08: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 19:35:09: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.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 19:35:09: #1 read tag files... INFO @ Fri, 05 Jul 2019 19:35:09: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 19:35:11: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.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 19:35:11: #1 read tag files... INFO @ Fri, 05 Jul 2019 19:35:11: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 19:35:16: 1000000 INFO @ Fri, 05 Jul 2019 19:35:17: 1000000 INFO @ Fri, 05 Jul 2019 19:35:19: 1000000 INFO @ Fri, 05 Jul 2019 19:35:25: 2000000 INFO @ Fri, 05 Jul 2019 19:35:25: 2000000 INFO @ Fri, 05 Jul 2019 19:35:27: 2000000 INFO @ Fri, 05 Jul 2019 19:35:32: 3000000 INFO @ Fri, 05 Jul 2019 19:35:33: 3000000 INFO @ Fri, 05 Jul 2019 19:35:36: 3000000 INFO @ Fri, 05 Jul 2019 19:35:40: 4000000 INFO @ Fri, 05 Jul 2019 19:35:41: 4000000 INFO @ Fri, 05 Jul 2019 19:35:44: 4000000 INFO @ Fri, 05 Jul 2019 19:35:46: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 19:35:47: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 19:35:47: #1 total tags in treatment: 4941410 INFO @ Fri, 05 Jul 2019 19:35:47: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 19:35:47: #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 19:35:48: #1 tags after filtering in treatment: 4941410 INFO @ Fri, 05 Jul 2019 19:35:48: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 19:35:48: #1 finished! INFO @ Fri, 05 Jul 2019 19:35:48: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 19:35:48: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 19:35:48: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 19:35:48: 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 19:35:48: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.05_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/ERX769125/ERX769125.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 19:35:48: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 19:35:48: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 19:35:48: #1 total tags in treatment: 4941410 INFO @ Fri, 05 Jul 2019 19:35:48: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 19:35:48: #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 19:35:48: #1 tags after filtering in treatment: 4941410 INFO @ Fri, 05 Jul 2019 19:35:48: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 19:35:48: #1 finished! INFO @ Fri, 05 Jul 2019 19:35:48: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 19:35:48: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 19:35:49: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 19:35:49: 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 19:35:49: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.10_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/ERX769125/ERX769125.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 19:35:51: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 19:35:51: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 19:35:51: #1 total tags in treatment: 4941410 INFO @ Fri, 05 Jul 2019 19:35:51: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 19:35:51: #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 19:35:51: #1 tags after filtering in treatment: 4941410 INFO @ Fri, 05 Jul 2019 19:35:51: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 19:35:51: #1 finished! INFO @ Fri, 05 Jul 2019 19:35:51: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 19:35:51: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 19:35:51: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 19:35:51: 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 19:35:51: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.20_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/ERX769125/ERX769125.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX769125/ERX769125.20_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。