Job ID = 9160060 sra ファイルのダウンロード中... Completed: 85791K bytes transferred in 4 seconds (154999K bits/sec), in 1 file, 2 directories. 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... Written 3779132 spots for /home/okishinya/chipatlas/results/sacCer3/SRX2619006/SRR5319591.sra Written 3779132 spots total 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: 00:00:40 3779132 reads; of these: 3779132 (100.00%) were unpaired; of these: 221063 (5.85%) aligned 0 times 2595515 (68.68%) aligned exactly 1 time 962554 (25.47%) aligned >1 times 94.15% overall alignment rate Time searching: 00:00:40 Overall time: 00:00:40 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] 1084445 / 3558069 = 0.3048 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, 28 Jun 2017 01:49:15: # Command line: callpeak -t SRX2619006.bam -f BAM -g 12100000 -n SRX2619006.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX2619006.10 # format = BAM # ChIP-seq file = ['SRX2619006.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, 28 Jun 2017 01:49:15: #1 read tag files... INFO @ Wed, 28 Jun 2017 01:49:15: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 01:49:15: # Command line: callpeak -t SRX2619006.bam -f BAM -g 12100000 -n SRX2619006.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX2619006.20 # format = BAM # ChIP-seq file = ['SRX2619006.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, 28 Jun 2017 01:49:15: #1 read tag files... INFO @ Wed, 28 Jun 2017 01:49:15: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 01:49:15: # Command line: callpeak -t SRX2619006.bam -f BAM -g 12100000 -n SRX2619006.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX2619006.05 # format = BAM # ChIP-seq file = ['SRX2619006.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, 28 Jun 2017 01:49:15: #1 read tag files... INFO @ Wed, 28 Jun 2017 01:49:15: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 01:49:21: 1000000 INFO @ Wed, 28 Jun 2017 01:49:21: 1000000 INFO @ Wed, 28 Jun 2017 01:49:21: 1000000 INFO @ Wed, 28 Jun 2017 01:49:27: 2000000 INFO @ Wed, 28 Jun 2017 01:49:27: 2000000 INFO @ Wed, 28 Jun 2017 01:49:27: 2000000 INFO @ Wed, 28 Jun 2017 01:49:30: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 01:49:30: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 01:49:30: #1 total tags in treatment: 2473624 INFO @ Wed, 28 Jun 2017 01:49:30: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 01:49:30: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 28 Jun 2017 01:49:30: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 01:49:30: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 01:49:30: #1 total tags in treatment: 2473624 INFO @ Wed, 28 Jun 2017 01:49:30: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 01:49:30: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 28 Jun 2017 01:49:30: #1 tags after filtering in treatment: 2473624 INFO @ Wed, 28 Jun 2017 01:49:30: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 01:49:30: #1 finished! INFO @ Wed, 28 Jun 2017 01:49:30: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 01:49:30: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 01:49:30: #1 tags after filtering in treatment: 2473624 INFO @ Wed, 28 Jun 2017 01:49:30: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 01:49:30: #1 finished! INFO @ Wed, 28 Jun 2017 01:49:30: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 01:49:30: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 01:49:30: #2 number of paired peaks: 41 WARNING @ Wed, 28 Jun 2017 01:49:30: Too few paired peaks (41) 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, 28 Jun 2017 01:49:30: Process for pairing-model is terminated! INFO @ Wed, 28 Jun 2017 01:49:30: #2 number of paired peaks: 41 WARNING @ Wed, 28 Jun 2017 01:49:30: Too few paired peaks (41) 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, 28 Jun 2017 01:49:30: Process for pairing-model is terminated! cat: SRX2619006.05_peaks.narrowPeak: そのようなファイルやディレクトリはありません cat: SRX2619006.20_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 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 `SRX2619006.20_model.r'rm: cannot remove `SRX2619006.05_model.r': そのようなファイルやディレクトリはありません : 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 `SRX2619006.20_*.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 `SRX2619006.05_*.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 `SRX2619006.20_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 `SRX2619006.05_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 CompletedMACS2peakCalling INFO @ Wed, 28 Jun 2017 01:49:30: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 01:49:30: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 01:49:30: #1 total tags in treatment: 2473624 INFO @ Wed, 28 Jun 2017 01:49:30: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 01:49:30: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 28 Jun 2017 01:49:30: #1 tags after filtering in treatment: 2473624 INFO @ Wed, 28 Jun 2017 01:49:30: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 01:49:30: #1 finished! INFO @ Wed, 28 Jun 2017 01:49:30: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 01:49:30: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 01:49:30: #2 number of paired peaks: 41 WARNING @ Wed, 28 Jun 2017 01:49:30: Too few paired peaks (41) 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, 28 Jun 2017 01:49:30: Process for pairing-model is terminated! cat: SRX2619006.10_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 `SRX2619006.10_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 `SRX2619006.10_*.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 `SRX2619006.10_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 BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。