Job ID = 2010984 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2019-07-05T16:34:32 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 ) 2019-07-05T16:34:32 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 ) 2019-07-05T16:34:32 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 : 11,035,192 reads read : 22,070,384 reads written : 11,035,192 reads 0-length : 11,035,192 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: 00:02:03 11035192 reads; of these: 11035192 (100.00%) were unpaired; of these: 2302865 (20.87%) aligned 0 times 7950023 (72.04%) aligned exactly 1 time 782304 (7.09%) aligned >1 times 79.13% overall alignment rate Time searching: 00:02:03 Overall time: 00:02:03 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] 2468163 / 8732327 = 0.2826 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 01:41:27: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.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 01:41:27: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:41:27: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:41:28: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.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 01:41:28: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:41:28: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:41:35: 1000000 INFO @ Sat, 06 Jul 2019 01:41:37: 1000000 INFO @ Sat, 06 Jul 2019 01:41:43: 2000000 INFO @ Sat, 06 Jul 2019 01:41:44: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.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 01:41:44: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:41:44: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:41:46: 2000000 INFO @ Sat, 06 Jul 2019 01:41:51: 3000000 INFO @ Sat, 06 Jul 2019 01:41:53: 1000000 INFO @ Sat, 06 Jul 2019 01:41:54: 3000000 INFO @ Sat, 06 Jul 2019 01:41:59: 4000000 INFO @ Sat, 06 Jul 2019 01:42:02: 2000000 INFO @ Sat, 06 Jul 2019 01:42:03: 4000000 INFO @ Sat, 06 Jul 2019 01:42:06: 5000000 INFO @ Sat, 06 Jul 2019 01:42:10: 3000000 INFO @ Sat, 06 Jul 2019 01:42:11: 5000000 INFO @ Sat, 06 Jul 2019 01:42:13: 6000000 INFO @ Sat, 06 Jul 2019 01:42:17: #1 tag size is determined as 66 bps INFO @ Sat, 06 Jul 2019 01:42:17: #1 tag size = 66 INFO @ Sat, 06 Jul 2019 01:42:17: #1 total tags in treatment: 6264164 INFO @ Sat, 06 Jul 2019 01:42:17: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:42:17: #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 01:42:17: #1 tags after filtering in treatment: 6264164 INFO @ Sat, 06 Jul 2019 01:42:17: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:42:17: #1 finished! INFO @ Sat, 06 Jul 2019 01:42:17: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:42:17: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:42:17: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:42:17: 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 01:42:17: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.05_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/SRX4342632/SRX4342632.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 01:42:19: 4000000 INFO @ Sat, 06 Jul 2019 01:42:19: 6000000 INFO @ Sat, 06 Jul 2019 01:42:21: #1 tag size is determined as 66 bps INFO @ Sat, 06 Jul 2019 01:42:21: #1 tag size = 66 INFO @ Sat, 06 Jul 2019 01:42:21: #1 total tags in treatment: 6264164 INFO @ Sat, 06 Jul 2019 01:42:21: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:42:21: #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 01:42:21: #1 tags after filtering in treatment: 6264164 INFO @ Sat, 06 Jul 2019 01:42:21: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:42:21: #1 finished! INFO @ Sat, 06 Jul 2019 01:42:21: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:42:21: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:42:21: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:42:21: 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 01:42:21: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.10_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/SRX4342632/SRX4342632.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 01:42:27: 5000000 INFO @ Sat, 06 Jul 2019 01:42:35: 6000000 INFO @ Sat, 06 Jul 2019 01:42:37: #1 tag size is determined as 66 bps INFO @ Sat, 06 Jul 2019 01:42:37: #1 tag size = 66 INFO @ Sat, 06 Jul 2019 01:42:37: #1 total tags in treatment: 6264164 INFO @ Sat, 06 Jul 2019 01:42:37: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:42:37: #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 01:42:37: #1 tags after filtering in treatment: 6264164 INFO @ Sat, 06 Jul 2019 01:42:37: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:42:37: #1 finished! INFO @ Sat, 06 Jul 2019 01:42:37: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:42:37: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:42:37: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:42:37: 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 01:42:37: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.20_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/SRX4342632/SRX4342632.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4342632/SRX4342632.20_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。