Job ID = 11245240 sra ファイルのダウンロード中... Completed: 609314K bytes transferred in 7 seconds (626849K 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 22139883 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4717382/SRR7878705.sra Written 22139883 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4717382/SRR7878705.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: 00:04:03 22139883 reads; of these: 22139883 (100.00%) were unpaired; of these: 6073511 (27.43%) aligned 0 times 13610919 (61.48%) aligned exactly 1 time 2455453 (11.09%) aligned >1 times 72.57% overall alignment rate Time searching: 00:04:03 Overall time: 00:04:03 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_sort_core] merging from 8 files... [bam_rmdupse_core] 5987470 / 16066372 = 0.3727 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 @ Wed, 10 Oct 2018 00:06:32: # Command line: callpeak -t SRX4717382.bam -f BAM -g 12100000 -n SRX4717382.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX4717382.20 # format = BAM # ChIP-seq file = ['SRX4717382.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 @ Wed, 10 Oct 2018 00:06:32: #1 read tag files... INFO @ Wed, 10 Oct 2018 00:06:32: #1 read treatment tags... INFO @ Wed, 10 Oct 2018 00:06:32: # Command line: callpeak -t SRX4717382.bam -f BAM -g 12100000 -n SRX4717382.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX4717382.10 # format = BAM # ChIP-seq file = ['SRX4717382.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 @ Wed, 10 Oct 2018 00:06:32: #1 read tag files... INFO @ Wed, 10 Oct 2018 00:06:32: #1 read treatment tags... INFO @ Wed, 10 Oct 2018 00:06:32: # Command line: callpeak -t SRX4717382.bam -f BAM -g 12100000 -n SRX4717382.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX4717382.05 # format = BAM # ChIP-seq file = ['SRX4717382.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 @ Wed, 10 Oct 2018 00:06:32: #1 read tag files... INFO @ Wed, 10 Oct 2018 00:06:32: #1 read treatment tags... INFO @ Wed, 10 Oct 2018 00:06:39: 1000000 INFO @ Wed, 10 Oct 2018 00:06:39: 1000000 INFO @ Wed, 10 Oct 2018 00:06:39: 1000000 INFO @ Wed, 10 Oct 2018 00:06:46: 2000000 INFO @ Wed, 10 Oct 2018 00:06:47: 2000000 INFO @ Wed, 10 Oct 2018 00:06:47: 2000000 INFO @ Wed, 10 Oct 2018 00:06:53: 3000000 INFO @ Wed, 10 Oct 2018 00:06:54: 3000000 INFO @ Wed, 10 Oct 2018 00:06:54: 3000000 INFO @ Wed, 10 Oct 2018 00:07:00: 4000000 INFO @ Wed, 10 Oct 2018 00:07:01: 4000000 INFO @ Wed, 10 Oct 2018 00:07:01: 4000000 INFO @ Wed, 10 Oct 2018 00:07:07: 5000000 INFO @ Wed, 10 Oct 2018 00:07:08: 5000000 INFO @ Wed, 10 Oct 2018 00:07:08: 5000000 INFO @ Wed, 10 Oct 2018 00:07:14: 6000000 INFO @ Wed, 10 Oct 2018 00:07:15: 6000000 INFO @ Wed, 10 Oct 2018 00:07:15: 6000000 INFO @ Wed, 10 Oct 2018 00:07:21: 7000000 INFO @ Wed, 10 Oct 2018 00:07:22: 7000000 INFO @ Wed, 10 Oct 2018 00:07:22: 7000000 INFO @ Wed, 10 Oct 2018 00:07:28: 8000000 INFO @ Wed, 10 Oct 2018 00:07:30: 8000000 INFO @ Wed, 10 Oct 2018 00:07:30: 8000000 INFO @ Wed, 10 Oct 2018 00:07:36: 9000000 INFO @ Wed, 10 Oct 2018 00:07:37: 9000000 INFO @ Wed, 10 Oct 2018 00:07:37: 9000000 INFO @ Wed, 10 Oct 2018 00:07:43: 10000000 INFO @ Wed, 10 Oct 2018 00:07:43: #1 tag size is determined as 76 bps INFO @ Wed, 10 Oct 2018 00:07:43: #1 tag size = 76 INFO @ Wed, 10 Oct 2018 00:07:43: #1 total tags in treatment: 10078902 INFO @ Wed, 10 Oct 2018 00:07:43: #1 user defined the maximum tags... INFO @ Wed, 10 Oct 2018 00:07:43: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 10 Oct 2018 00:07:43: #1 tags after filtering in treatment: 10078902 INFO @ Wed, 10 Oct 2018 00:07:43: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 10 Oct 2018 00:07:43: #1 finished! INFO @ Wed, 10 Oct 2018 00:07:43: #2 Build Peak Model... INFO @ Wed, 10 Oct 2018 00:07:43: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 10 Oct 2018 00:07:44: 10000000 INFO @ Wed, 10 Oct 2018 00:07:44: #1 tag size is determined as 76 bps INFO @ Wed, 10 Oct 2018 00:07:44: #1 tag size = 76 INFO @ Wed, 10 Oct 2018 00:07:44: #1 total tags in treatment: 10078902 INFO @ Wed, 10 Oct 2018 00:07:44: #1 user defined the maximum tags... INFO @ Wed, 10 Oct 2018 00:07:44: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 10 Oct 2018 00:07:44: #2 number of paired peaks: 0 WARNING @ Wed, 10 Oct 2018 00:07:44: 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 @ Wed, 10 Oct 2018 00:07:44: Process for pairing-model is terminated! cat: SRX4717382.05_peaks.narrowPeak: そのようなファイルやディレクトリはありません pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4717382.05_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 `SRX4717382.05_*.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 `SRX4717382.05_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 INFO @ Wed, 10 Oct 2018 00:07:44: 10000000 INFO @ Wed, 10 Oct 2018 00:07:44: #1 tags after filtering in treatment: 10078902 INFO @ Wed, 10 Oct 2018 00:07:44: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 10 Oct 2018 00:07:44: #1 finished! INFO @ Wed, 10 Oct 2018 00:07:44: #2 Build Peak Model... INFO @ Wed, 10 Oct 2018 00:07:44: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 10 Oct 2018 00:07:45: #1 tag size is determined as 76 bps INFO @ Wed, 10 Oct 2018 00:07:45: #1 tag size = 76 INFO @ Wed, 10 Oct 2018 00:07:45: #1 total tags in treatment: 10078902 INFO @ Wed, 10 Oct 2018 00:07:45: #1 user defined the maximum tags... INFO @ Wed, 10 Oct 2018 00:07:45: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 10 Oct 2018 00:07:45: #2 number of paired peaks: 0 WARNING @ Wed, 10 Oct 2018 00:07:45: 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 @ Wed, 10 Oct 2018 00:07:45: Process for pairing-model is terminated! cat: SRX4717382.10_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): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4717382.10_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 `SRX4717382.10_*.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 `SRX4717382.10_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 @ Wed, 10 Oct 2018 00:07:45: #1 tags after filtering in treatment: 10078902 INFO @ Wed, 10 Oct 2018 00:07:45: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 10 Oct 2018 00:07:45: #1 finished! INFO @ Wed, 10 Oct 2018 00:07:45: #2 Build Peak Model... INFO @ Wed, 10 Oct 2018 00:07:45: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 10 Oct 2018 00:07:46: #2 number of paired peaks: 0 WARNING @ Wed, 10 Oct 2018 00:07:46: 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 @ Wed, 10 Oct 2018 00:07:46: Process for pairing-model is terminated! cat: SRX4717382.20_peaks.narrowPeak: そのようなファイルやディレクトリはありません pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4717382.20_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 `SRX4717382.20_*.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 `SRX4717382.20_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。