Job ID = 11634691 sra ファイルのダウンロード中... Completed: 300590K bytes transferred in 5 seconds (430061K bits/sec), in 1 file. sra ファイルのダウンロードが完了しました。 Read layout: SINGLE fastq に変換中... Read 15591381 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4092971/SRR7175399.sra Written 15591381 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4092971/SRR7175399.sra rm: cannot remove `[DSE]RX*': そのようなファイルやディレクトリはありません rm: cannot remove `[DSE]RR*.fastq': そのようなファイルやディレクトリはありません 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: 00:02:29 15591381 reads; of these: 15591381 (100.00%) were unpaired; of these: 1621532 (10.40%) aligned 0 times 10836612 (69.50%) aligned exactly 1 time 3133237 (20.10%) aligned >1 times 89.60% overall alignment rate Time searching: 00:02:29 Overall time: 00:02:29 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] 5390406 / 13969849 = 0.3859 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, 15 Feb 2019 10:41:54: # Command line: callpeak -t SRX4092971.bam -f BAM -g 12100000 -n SRX4092971.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX4092971.10 # format = BAM # ChIP-seq file = ['SRX4092971.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, 15 Feb 2019 10:41:54: #1 read tag files... INFO @ Fri, 15 Feb 2019 10:41:54: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 10:41:54: # Command line: callpeak -t SRX4092971.bam -f BAM -g 12100000 -n SRX4092971.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX4092971.20 # format = BAM # ChIP-seq file = ['SRX4092971.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, 15 Feb 2019 10:41:54: #1 read tag files... INFO @ Fri, 15 Feb 2019 10:41:54: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 10:41:54: # Command line: callpeak -t SRX4092971.bam -f BAM -g 12100000 -n SRX4092971.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX4092971.05 # format = BAM # ChIP-seq file = ['SRX4092971.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, 15 Feb 2019 10:41:54: #1 read tag files... INFO @ Fri, 15 Feb 2019 10:41:54: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 10:42:01: 1000000 INFO @ Fri, 15 Feb 2019 10:42:01: 1000000 INFO @ Fri, 15 Feb 2019 10:42:01: 1000000 INFO @ Fri, 15 Feb 2019 10:42:08: 2000000 INFO @ Fri, 15 Feb 2019 10:42:08: 2000000 INFO @ Fri, 15 Feb 2019 10:42:08: 2000000 INFO @ Fri, 15 Feb 2019 10:42:14: 3000000 INFO @ Fri, 15 Feb 2019 10:42:14: 3000000 INFO @ Fri, 15 Feb 2019 10:42:14: 3000000 INFO @ Fri, 15 Feb 2019 10:42:21: 4000000 INFO @ Fri, 15 Feb 2019 10:42:21: 4000000 INFO @ Fri, 15 Feb 2019 10:42:21: 4000000 INFO @ Fri, 15 Feb 2019 10:42:27: 5000000 INFO @ Fri, 15 Feb 2019 10:42:28: 5000000 INFO @ Fri, 15 Feb 2019 10:42:28: 5000000 INFO @ Fri, 15 Feb 2019 10:42:34: 6000000 INFO @ Fri, 15 Feb 2019 10:42:35: 6000000 INFO @ Fri, 15 Feb 2019 10:42:35: 6000000 INFO @ Fri, 15 Feb 2019 10:42:41: 7000000 INFO @ Fri, 15 Feb 2019 10:42:42: 7000000 INFO @ Fri, 15 Feb 2019 10:42:42: 7000000 INFO @ Fri, 15 Feb 2019 10:42:47: 8000000 INFO @ Fri, 15 Feb 2019 10:42:49: 8000000 INFO @ Fri, 15 Feb 2019 10:42:49: 8000000 INFO @ Fri, 15 Feb 2019 10:42:51: #1 tag size is determined as 50 bps INFO @ Fri, 15 Feb 2019 10:42:51: #1 tag size = 50 INFO @ Fri, 15 Feb 2019 10:42:51: #1 total tags in treatment: 8579443 INFO @ Fri, 15 Feb 2019 10:42:51: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 10:42:51: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 10:42:51: #1 tags after filtering in treatment: 8579443 INFO @ Fri, 15 Feb 2019 10:42:51: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 10:42:51: #1 finished! INFO @ Fri, 15 Feb 2019 10:42:51: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 10:42:51: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 10:42:52: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 10:42:52: 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, 15 Feb 2019 10:42:52: Process for pairing-model is terminated! cat: SRX4092971.10_peaks.narrowPeak: そのようなファイルやディレクトリはありません pass1 - making usageList (0 chroms): 4 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4092971.10_model.r': そのようなファイルやディレクトリはありません rm: cannot remove `SRX4092971.10_*.xls': そのようなファイルやディレクトリはありません rm: cannot remove `SRX4092971.10_peaks.narrowPeak': そのようなファイルやディレクトリはありません CompletedMACS2peakCalling INFO @ Fri, 15 Feb 2019 10:42:52: #1 tag size is determined as 50 bps INFO @ Fri, 15 Feb 2019 10:42:52: #1 tag size = 50 INFO @ Fri, 15 Feb 2019 10:42:52: #1 total tags in treatment: 8579443 INFO @ Fri, 15 Feb 2019 10:42:52: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 10:42:52: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 10:42:52: #1 tag size is determined as 50 bps INFO @ Fri, 15 Feb 2019 10:42:52: #1 tag size = 50 INFO @ Fri, 15 Feb 2019 10:42:52: #1 total tags in treatment: 8579443 INFO @ Fri, 15 Feb 2019 10:42:52: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 10:42:52: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 10:42:53: #1 tags after filtering in treatment: 8579443 INFO @ Fri, 15 Feb 2019 10:42:53: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 10:42:53: #1 finished! INFO @ Fri, 15 Feb 2019 10:42:53: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 10:42:53: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 10:42:53: #1 tags after filtering in treatment: 8579443 INFO @ Fri, 15 Feb 2019 10:42:53: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 10:42:53: #1 finished! INFO @ Fri, 15 Feb 2019 10:42:53: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 10:42:53: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 10:42:53: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 10:42:53: 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, 15 Feb 2019 10:42:53: Process for pairing-model is terminated! cat: SRX4092971.05_peaks.narrowPeak: そのようなファイルやディレクトリはありません INFO @ Fri, 15 Feb 2019 10:42:53: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 10:42:53: 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, 15 Feb 2019 10:42:53: Process for pairing-model is terminated! pass1 - making usageList (0 chroms): 5 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) cat: SRX4092971.20_peaks.narrowPeak: そのようなファイルやディレクトリはありません rm: cannot remove `SRX4092971.05_model.r': そのようなファイルやディレクトリはありません rm: cannot remove `SRX4092971.05_*.xls': そのようなファイルやディレクトリはありません rm: cannot remove `SRX4092971.05_peaks.narrowPeak': そのようなファイルやディレクトリはありません CompletedMACS2peakCalling pass1 - making usageList (0 chroms): 3 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4092971.20_model.r': そのようなファイルやディレクトリはありません rm: cannot remove `SRX4092971.20_*.xls': そのようなファイルやディレクトリはありません rm: cannot remove `SRX4092971.20_peaks.narrowPeak': そのようなファイルやディレクトリはありません CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。