Job ID = 11192620 sra ファイルのダウンロード中... Completed: 384355K bytes transferred in 6 seconds (459035K 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 10658277 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1143274/SRR2156286.sra Written 10658277 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1143274/SRR2156286.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: 00:02:34 10658277 reads; of these: 10658277 (100.00%) were unpaired; of these: 1140961 (10.70%) aligned 0 times 8706536 (81.69%) aligned exactly 1 time 810780 (7.61%) aligned >1 times 89.30% overall alignment rate Time searching: 00:02:34 Overall time: 00:02:35 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] 2660237 / 9517316 = 0.2795 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, 15 Sep 2018 09:38:14: # Command line: callpeak -t SRX1143274.bam -f BAM -g 12100000 -n SRX1143274.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX1143274.10 # format = BAM # ChIP-seq file = ['SRX1143274.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, 15 Sep 2018 09:38:14: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:38:14: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:38:14: # Command line: callpeak -t SRX1143274.bam -f BAM -g 12100000 -n SRX1143274.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX1143274.20 # format = BAM # ChIP-seq file = ['SRX1143274.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, 15 Sep 2018 09:38:14: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:38:14: # Command line: callpeak -t SRX1143274.bam -f BAM -g 12100000 -n SRX1143274.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX1143274.05 # format = BAM # ChIP-seq file = ['SRX1143274.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, 15 Sep 2018 09:38:14: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:38:14: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:38:14: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:38:21: 1000000 INFO @ Sat, 15 Sep 2018 09:38:21: 1000000 INFO @ Sat, 15 Sep 2018 09:38:21: 1000000 INFO @ Sat, 15 Sep 2018 09:38:28: 2000000 INFO @ Sat, 15 Sep 2018 09:38:28: 2000000 INFO @ Sat, 15 Sep 2018 09:38:28: 2000000 INFO @ Sat, 15 Sep 2018 09:38:35: 3000000 INFO @ Sat, 15 Sep 2018 09:38:35: 3000000 INFO @ Sat, 15 Sep 2018 09:38:35: 3000000 INFO @ Sat, 15 Sep 2018 09:38:42: 4000000 INFO @ Sat, 15 Sep 2018 09:38:42: 4000000 INFO @ Sat, 15 Sep 2018 09:38:42: 4000000 INFO @ Sat, 15 Sep 2018 09:38:48: 5000000 INFO @ Sat, 15 Sep 2018 09:38:48: 5000000 INFO @ Sat, 15 Sep 2018 09:38:49: 5000000 INFO @ Sat, 15 Sep 2018 09:38:55: 6000000 INFO @ Sat, 15 Sep 2018 09:38:55: 6000000 INFO @ Sat, 15 Sep 2018 09:38:56: 6000000 INFO @ Sat, 15 Sep 2018 09:39:01: #1 tag size is determined as 75 bps INFO @ Sat, 15 Sep 2018 09:39:01: #1 tag size = 75 INFO @ Sat, 15 Sep 2018 09:39:01: #1 total tags in treatment: 6857079 INFO @ Sat, 15 Sep 2018 09:39:01: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:39:01: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 09:39:01: #1 tag size is determined as 75 bps INFO @ Sat, 15 Sep 2018 09:39:01: #1 tag size = 75 INFO @ Sat, 15 Sep 2018 09:39:01: #1 total tags in treatment: 6857079 INFO @ Sat, 15 Sep 2018 09:39:01: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:39:01: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 09:39:01: #1 tags after filtering in treatment: 6857079 INFO @ Sat, 15 Sep 2018 09:39:01: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Sep 2018 09:39:01: #1 finished! INFO @ Sat, 15 Sep 2018 09:39:01: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:39:01: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:39:01: #1 tags after filtering in treatment: 6857079 INFO @ Sat, 15 Sep 2018 09:39:01: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Sep 2018 09:39:01: #1 finished! INFO @ Sat, 15 Sep 2018 09:39:01: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:39:01: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:39:02: #2 number of paired peaks: 0 WARNING @ Sat, 15 Sep 2018 09:39:02: 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, 15 Sep 2018 09:39:02: Process for pairing-model is terminated! INFO @ Sat, 15 Sep 2018 09:39:02: #2 number of paired peaks: 0 WARNING @ Sat, 15 Sep 2018 09:39:02: 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, 15 Sep 2018 09:39:02: Process for pairing-model is terminated! cat: cat: SRX1143274.10_peaks.narrowPeakSRX1143274.05_peaks.narrowPeak: そのようなファイルやディレクトリはありません: 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 pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX1143274.05_model.r'rm: : そのようなファイルやディレクトリはありませんcannot remove `SRX1143274.10_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 `SRX1143274.05_*.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 `SRX1143274.10_*.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 `SRX1143274.05_peaks.narrowPeak': そのようなファイルやディレクトリはありません rm: cannot remove `SRX1143274.10_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 CompletedMACS2peakCalling INFO @ Sat, 15 Sep 2018 09:39:02: #1 tag size is determined as 75 bps INFO @ Sat, 15 Sep 2018 09:39:02: #1 tag size = 75 INFO @ Sat, 15 Sep 2018 09:39:02: #1 total tags in treatment: 6857079 INFO @ Sat, 15 Sep 2018 09:39:02: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:39:02: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 09:39:02: #1 tags after filtering in treatment: 6857079 INFO @ Sat, 15 Sep 2018 09:39:02: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Sep 2018 09:39:02: #1 finished! INFO @ Sat, 15 Sep 2018 09:39:02: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:39:02: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:39:02: #2 number of paired peaks: 0 WARNING @ Sat, 15 Sep 2018 09:39:02: 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, 15 Sep 2018 09:39:02: Process for pairing-model is terminated! cat: SRX1143274.20_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 `SRX1143274.20_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 `SRX1143274.20_*.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 `SRX1143274.20_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。