Job ID = 11162596 sra ファイルのダウンロード中... Completed: 781832K bytes transferred in 20 seconds (308627K 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 42931548 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3585206/SRR6495906.sra Written 42931548 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3585206/SRR6495906.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: 00:06:09 42931548 reads; of these: 42931548 (100.00%) were unpaired; of these: 12938075 (30.14%) aligned 0 times 27020164 (62.94%) aligned exactly 1 time 2973309 (6.93%) aligned >1 times 69.86% overall alignment rate Time searching: 00:06:09 Overall time: 00:06:09 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 16 files... [bam_rmdupse_core] 18204407 / 29993473 = 0.6069 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, 05 Sep 2018 10:32:30: # Command line: callpeak -t SRX3585206.bam -f BAM -g 12100000 -n SRX3585206.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3585206.10 # format = BAM # ChIP-seq file = ['SRX3585206.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, 05 Sep 2018 10:32:30: #1 read tag files... INFO @ Wed, 05 Sep 2018 10:32:30: #1 read treatment tags... INFO @ Wed, 05 Sep 2018 10:32:30: # Command line: callpeak -t SRX3585206.bam -f BAM -g 12100000 -n SRX3585206.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3585206.05 # format = BAM # ChIP-seq file = ['SRX3585206.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, 05 Sep 2018 10:32:30: #1 read tag files... INFO @ Wed, 05 Sep 2018 10:32:30: #1 read treatment tags... INFO @ Wed, 05 Sep 2018 10:32:30: # Command line: callpeak -t SRX3585206.bam -f BAM -g 12100000 -n SRX3585206.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3585206.20 # format = BAM # ChIP-seq file = ['SRX3585206.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, 05 Sep 2018 10:32:30: #1 read tag files... INFO @ Wed, 05 Sep 2018 10:32:30: #1 read treatment tags... INFO @ Wed, 05 Sep 2018 10:32:36: 1000000 INFO @ Wed, 05 Sep 2018 10:32:36: 1000000 INFO @ Wed, 05 Sep 2018 10:32:36: 1000000 INFO @ Wed, 05 Sep 2018 10:32:42: 2000000 INFO @ Wed, 05 Sep 2018 10:32:42: 2000000 INFO @ Wed, 05 Sep 2018 10:32:42: 2000000 INFO @ Wed, 05 Sep 2018 10:32:47: 3000000 INFO @ Wed, 05 Sep 2018 10:32:48: 3000000 INFO @ Wed, 05 Sep 2018 10:32:48: 3000000 INFO @ Wed, 05 Sep 2018 10:32:53: 4000000 INFO @ Wed, 05 Sep 2018 10:32:54: 4000000 INFO @ Wed, 05 Sep 2018 10:32:54: 4000000 INFO @ Wed, 05 Sep 2018 10:32:59: 5000000 INFO @ Wed, 05 Sep 2018 10:33:00: 5000000 INFO @ Wed, 05 Sep 2018 10:33:00: 5000000 INFO @ Wed, 05 Sep 2018 10:33:05: 6000000 INFO @ Wed, 05 Sep 2018 10:33:06: 6000000 INFO @ Wed, 05 Sep 2018 10:33:06: 6000000 INFO @ Wed, 05 Sep 2018 10:33:11: 7000000 INFO @ Wed, 05 Sep 2018 10:33:12: 7000000 INFO @ Wed, 05 Sep 2018 10:33:12: 7000000 INFO @ Wed, 05 Sep 2018 10:33:17: 8000000 INFO @ Wed, 05 Sep 2018 10:33:17: 8000000 INFO @ Wed, 05 Sep 2018 10:33:18: 8000000 INFO @ Wed, 05 Sep 2018 10:33:23: 9000000 INFO @ Wed, 05 Sep 2018 10:33:23: 9000000 INFO @ Wed, 05 Sep 2018 10:33:24: 9000000 INFO @ Wed, 05 Sep 2018 10:33:29: 10000000 INFO @ Wed, 05 Sep 2018 10:33:29: 10000000 INFO @ Wed, 05 Sep 2018 10:33:30: 10000000 INFO @ Wed, 05 Sep 2018 10:33:34: 11000000 INFO @ Wed, 05 Sep 2018 10:33:35: 11000000 INFO @ Wed, 05 Sep 2018 10:33:36: 11000000 INFO @ Wed, 05 Sep 2018 10:33:39: #1 tag size is determined as 50 bps INFO @ Wed, 05 Sep 2018 10:33:39: #1 tag size = 50 INFO @ Wed, 05 Sep 2018 10:33:39: #1 total tags in treatment: 11789066 INFO @ Wed, 05 Sep 2018 10:33:39: #1 user defined the maximum tags... INFO @ Wed, 05 Sep 2018 10:33:39: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 05 Sep 2018 10:33:39: #1 tags after filtering in treatment: 11789066 INFO @ Wed, 05 Sep 2018 10:33:39: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 05 Sep 2018 10:33:39: #1 finished! INFO @ Wed, 05 Sep 2018 10:33:39: #2 Build Peak Model... INFO @ Wed, 05 Sep 2018 10:33:39: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 05 Sep 2018 10:33:40: #2 number of paired peaks: 0 WARNING @ Wed, 05 Sep 2018 10:33:40: 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, 05 Sep 2018 10:33:40: Process for pairing-model is terminated! cat: SRX3585206.10_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 `SRX3585206.10_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 `SRX3585206.10_*.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 `SRX3585206.10_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, 05 Sep 2018 10:33:40: #1 tag size is determined as 50 bps INFO @ Wed, 05 Sep 2018 10:33:40: #1 tag size = 50 INFO @ Wed, 05 Sep 2018 10:33:40: #1 total tags in treatment: 11789066 INFO @ Wed, 05 Sep 2018 10:33:40: #1 user defined the maximum tags... INFO @ Wed, 05 Sep 2018 10:33:40: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 05 Sep 2018 10:33:40: #1 tags after filtering in treatment: 11789066 INFO @ Wed, 05 Sep 2018 10:33:40: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 05 Sep 2018 10:33:40: #1 finished! INFO @ Wed, 05 Sep 2018 10:33:40: #2 Build Peak Model... INFO @ Wed, 05 Sep 2018 10:33:40: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 05 Sep 2018 10:33:40: #1 tag size is determined as 50 bps INFO @ Wed, 05 Sep 2018 10:33:40: #1 tag size = 50 INFO @ Wed, 05 Sep 2018 10:33:40: #1 total tags in treatment: 11789066 INFO @ Wed, 05 Sep 2018 10:33:40: #1 user defined the maximum tags... INFO @ Wed, 05 Sep 2018 10:33:40: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 05 Sep 2018 10:33:41: #1 tags after filtering in treatment: 11789066 INFO @ Wed, 05 Sep 2018 10:33:41: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 05 Sep 2018 10:33:41: #1 finished! INFO @ Wed, 05 Sep 2018 10:33:41: #2 Build Peak Model... INFO @ Wed, 05 Sep 2018 10:33:41: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 05 Sep 2018 10:33:41: #2 number of paired peaks: 0 WARNING @ Wed, 05 Sep 2018 10:33:41: 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, 05 Sep 2018 10:33:41: Process for pairing-model is terminated! cat: SRX3585206.20_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 `SRX3585206.20_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 `SRX3585206.20_*.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 `SRX3585206.20_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 INFO @ Wed, 05 Sep 2018 10:33:41: #2 number of paired peaks: 0 WARNING @ Wed, 05 Sep 2018 10:33:41: 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, 05 Sep 2018 10:33:41: Process for pairing-model is terminated! cat: SRX3585206.05_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 `SRX3585206.05_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 `SRX3585206.05_*.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 `SRX3585206.05_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 BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。