Job ID = 11162615 sra ファイルのダウンロード中... Completed: 814600K bytes transferred in 9 seconds (723005K 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 26783017 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3585220/SRR6495920.sra Written 26783017 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3585220/SRR6495920.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: 00:04:05 26783017 reads; of these: 26783017 (100.00%) were unpaired; of these: 5861271 (21.88%) aligned 0 times 18673011 (69.72%) aligned exactly 1 time 2248735 (8.40%) aligned >1 times 78.12% overall alignment rate Time searching: 00:04:05 Overall time: 00:04:05 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 12 files... [bam_rmdupse_core] 10984772 / 20921746 = 0.5250 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 10:37:20: # Command line: callpeak -t SRX3585220.bam -f BAM -g 12100000 -n SRX3585220.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3585220.10 # format = BAM # ChIP-seq file = ['SRX3585220.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 10:37:20: #1 read tag files... INFO @ Wed, 05 Sep 2018 10:37:20: #1 read treatment tags... INFO @ Wed, 05 Sep 2018 10:37:20: # Command line: callpeak -t SRX3585220.bam -f BAM -g 12100000 -n SRX3585220.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3585220.20 # format = BAM # ChIP-seq file = ['SRX3585220.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 10:37:20: #1 read tag files... INFO @ Wed, 05 Sep 2018 10:37:20: #1 read treatment tags... INFO @ Wed, 05 Sep 2018 10:37:20: # Command line: callpeak -t SRX3585220.bam -f BAM -g 12100000 -n SRX3585220.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3585220.05 # format = BAM # ChIP-seq file = ['SRX3585220.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 10:37:20: #1 read tag files... INFO @ Wed, 05 Sep 2018 10:37:20: #1 read treatment tags... INFO @ Wed, 05 Sep 2018 10:37:26: 1000000 INFO @ Wed, 05 Sep 2018 10:37:26: 1000000 INFO @ Wed, 05 Sep 2018 10:37:26: 1000000 INFO @ Wed, 05 Sep 2018 10:37:32: 2000000 INFO @ Wed, 05 Sep 2018 10:37:32: 2000000 INFO @ Wed, 05 Sep 2018 10:37:32: 2000000 INFO @ Wed, 05 Sep 2018 10:37:38: 3000000 INFO @ Wed, 05 Sep 2018 10:37:38: 3000000 INFO @ Wed, 05 Sep 2018 10:37:39: 3000000 INFO @ Wed, 05 Sep 2018 10:37:44: 4000000 INFO @ Wed, 05 Sep 2018 10:37:45: 4000000 INFO @ Wed, 05 Sep 2018 10:37:45: 4000000 INFO @ Wed, 05 Sep 2018 10:37:50: 5000000 INFO @ Wed, 05 Sep 2018 10:37:51: 5000000 INFO @ Wed, 05 Sep 2018 10:37:52: 5000000 INFO @ Wed, 05 Sep 2018 10:37:56: 6000000 INFO @ Wed, 05 Sep 2018 10:37:57: 6000000 INFO @ Wed, 05 Sep 2018 10:37:58: 6000000 INFO @ Wed, 05 Sep 2018 10:38:02: 7000000 INFO @ Wed, 05 Sep 2018 10:38:04: 7000000 INFO @ Wed, 05 Sep 2018 10:38:05: 7000000 INFO @ Wed, 05 Sep 2018 10:38:07: 8000000 INFO @ Wed, 05 Sep 2018 10:38:10: 8000000 INFO @ Wed, 05 Sep 2018 10:38:12: 8000000 INFO @ Wed, 05 Sep 2018 10:38:13: 9000000 INFO @ Wed, 05 Sep 2018 10:38:16: 9000000 INFO @ Wed, 05 Sep 2018 10:38:18: 9000000 INFO @ Wed, 05 Sep 2018 10:38:19: #1 tag size is determined as 50 bps INFO @ Wed, 05 Sep 2018 10:38:19: #1 tag size = 50 INFO @ Wed, 05 Sep 2018 10:38:19: #1 total tags in treatment: 9936974 INFO @ Wed, 05 Sep 2018 10:38:19: #1 user defined the maximum tags... INFO @ Wed, 05 Sep 2018 10:38:19: #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 10:38:19: #1 tags after filtering in treatment: 9936974 INFO @ Wed, 05 Sep 2018 10:38:19: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 05 Sep 2018 10:38:19: #1 finished! INFO @ Wed, 05 Sep 2018 10:38:19: #2 Build Peak Model... INFO @ Wed, 05 Sep 2018 10:38:19: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 05 Sep 2018 10:38:20: #2 number of paired peaks: 0 WARNING @ Wed, 05 Sep 2018 10:38:20: 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 10:38:20: Process for pairing-model is terminated! cat: SRX3585220.10_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): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX3585220.10_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 `SRX3585220.10_*.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 `SRX3585220.10_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 10:38:22: #1 tag size is determined as 50 bps INFO @ Wed, 05 Sep 2018 10:38:22: #1 tag size = 50 INFO @ Wed, 05 Sep 2018 10:38:22: #1 total tags in treatment: 9936974 INFO @ Wed, 05 Sep 2018 10:38:22: #1 user defined the maximum tags... INFO @ Wed, 05 Sep 2018 10:38:22: #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 10:38:22: #1 tags after filtering in treatment: 9936974 INFO @ Wed, 05 Sep 2018 10:38:22: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 05 Sep 2018 10:38:22: #1 finished! INFO @ Wed, 05 Sep 2018 10:38:22: #2 Build Peak Model... INFO @ Wed, 05 Sep 2018 10:38:22: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 05 Sep 2018 10:38:23: #2 number of paired peaks: 0 WARNING @ Wed, 05 Sep 2018 10:38:23: 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 10:38:23: Process for pairing-model is terminated! cat: SRX3585220.20_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 `SRX3585220.20_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 `SRX3585220.20_*.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 `SRX3585220.20_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 10:38:25: #1 tag size is determined as 50 bps INFO @ Wed, 05 Sep 2018 10:38:25: #1 tag size = 50 INFO @ Wed, 05 Sep 2018 10:38:25: #1 total tags in treatment: 9936974 INFO @ Wed, 05 Sep 2018 10:38:25: #1 user defined the maximum tags... INFO @ Wed, 05 Sep 2018 10:38:25: #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 10:38:25: #1 tags after filtering in treatment: 9936974 INFO @ Wed, 05 Sep 2018 10:38:25: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 05 Sep 2018 10:38:25: #1 finished! INFO @ Wed, 05 Sep 2018 10:38:25: #2 Build Peak Model... INFO @ Wed, 05 Sep 2018 10:38:25: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 05 Sep 2018 10:38:25: #2 number of paired peaks: 0 WARNING @ Wed, 05 Sep 2018 10:38:25: 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 10:38:25: Process for pairing-model is terminated! cat: SRX3585220.05_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 `SRX3585220.05_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 `SRX3585220.05_*.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 `SRX3585220.05_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。