Job ID = 9163605 sra ファイルのダウンロード中... Completed: 695931K bytes transferred in 9 seconds (581691K 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 22879139 spots for /home/okishinya/chipatlas/results/sacCer3/SRX964228/SRR1924335.sra Written 22879139 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: 00:03:55 22879139 reads; of these: 22879139 (100.00%) were unpaired; of these: 1295527 (5.66%) aligned 0 times 17408657 (76.09%) aligned exactly 1 time 4174955 (18.25%) aligned >1 times 94.34% overall alignment rate Time searching: 00:03:55 Overall time: 00:03:55 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] 9157260 / 21583612 = 0.4243 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 11:13:37: # Command line: callpeak -t SRX964228.bam -f BAM -g 12100000 -n SRX964228.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX964228.20 # format = BAM # ChIP-seq file = ['SRX964228.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 11:13:37: #1 read tag files... INFO @ Wed, 28 Jun 2017 11:13:37: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 11:13:37: # Command line: callpeak -t SRX964228.bam -f BAM -g 12100000 -n SRX964228.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX964228.10 # format = BAM # ChIP-seq file = ['SRX964228.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 11:13:37: #1 read tag files... INFO @ Wed, 28 Jun 2017 11:13:37: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 11:13:37: # Command line: callpeak -t SRX964228.bam -f BAM -g 12100000 -n SRX964228.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX964228.05 # format = BAM # ChIP-seq file = ['SRX964228.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 11:13:37: #1 read tag files... INFO @ Wed, 28 Jun 2017 11:13:37: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 11:13:43: 1000000 INFO @ Wed, 28 Jun 2017 11:13:43: 1000000 INFO @ Wed, 28 Jun 2017 11:13:44: 1000000 INFO @ Wed, 28 Jun 2017 11:13:50: 2000000 INFO @ Wed, 28 Jun 2017 11:13:50: 2000000 INFO @ Wed, 28 Jun 2017 11:13:50: 2000000 INFO @ Wed, 28 Jun 2017 11:13:57: 3000000 INFO @ Wed, 28 Jun 2017 11:13:57: 3000000 INFO @ Wed, 28 Jun 2017 11:13:57: 3000000 INFO @ Wed, 28 Jun 2017 11:14:04: 4000000 INFO @ Wed, 28 Jun 2017 11:14:04: 4000000 INFO @ Wed, 28 Jun 2017 11:14:04: 4000000 INFO @ Wed, 28 Jun 2017 11:14:10: 5000000 INFO @ Wed, 28 Jun 2017 11:14:10: 5000000 INFO @ Wed, 28 Jun 2017 11:14:10: 5000000 INFO @ Wed, 28 Jun 2017 11:14:17: 6000000 INFO @ Wed, 28 Jun 2017 11:14:17: 6000000 INFO @ Wed, 28 Jun 2017 11:14:17: 6000000 INFO @ Wed, 28 Jun 2017 11:14:23: 7000000 INFO @ Wed, 28 Jun 2017 11:14:24: 7000000 INFO @ Wed, 28 Jun 2017 11:14:24: 7000000 INFO @ Wed, 28 Jun 2017 11:14:30: 8000000 INFO @ Wed, 28 Jun 2017 11:14:30: 8000000 INFO @ Wed, 28 Jun 2017 11:14:30: 8000000 INFO @ Wed, 28 Jun 2017 11:14:36: 9000000 INFO @ Wed, 28 Jun 2017 11:14:37: 9000000 INFO @ Wed, 28 Jun 2017 11:14:37: 9000000 INFO @ Wed, 28 Jun 2017 11:14:43: 10000000 INFO @ Wed, 28 Jun 2017 11:14:44: 10000000 INFO @ Wed, 28 Jun 2017 11:14:44: 10000000 INFO @ Wed, 28 Jun 2017 11:14:49: 11000000 INFO @ Wed, 28 Jun 2017 11:14:50: 11000000 INFO @ Wed, 28 Jun 2017 11:14:50: 11000000 INFO @ Wed, 28 Jun 2017 11:14:56: 12000000 INFO @ Wed, 28 Jun 2017 11:14:57: 12000000 INFO @ Wed, 28 Jun 2017 11:14:57: 12000000 INFO @ Wed, 28 Jun 2017 11:14:59: #1 tag size is determined as 49 bps INFO @ Wed, 28 Jun 2017 11:14:59: #1 tag size = 49 INFO @ Wed, 28 Jun 2017 11:14:59: #1 total tags in treatment: 12426352 INFO @ Wed, 28 Jun 2017 11:14:59: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 11:14:59: #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 11:14:59: #1 tags after filtering in treatment: 12426352 INFO @ Wed, 28 Jun 2017 11:14:59: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 11:14:59: #1 finished! INFO @ Wed, 28 Jun 2017 11:14:59: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 11:14:59: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 11:15:00: #1 tag size is determined as 49 bps INFO @ Wed, 28 Jun 2017 11:15:00: #1 tag size = 49 INFO @ Wed, 28 Jun 2017 11:15:00: #1 total tags in treatment: 12426352 INFO @ Wed, 28 Jun 2017 11:15:00: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 11:15:00: #1 tag size is determined as 49 bps INFO @ Wed, 28 Jun 2017 11:15:00: #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 11:15:00: #1 tag size = 49 INFO @ Wed, 28 Jun 2017 11:15:00: #1 total tags in treatment: 12426352 INFO @ Wed, 28 Jun 2017 11:15:00: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 11:15:00: #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 11:15:00: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 11:15:00: 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, 28 Jun 2017 11:15:00: Process for pairing-model is terminated! cat: SRX964228.10_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 `SRX964228.10_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 `SRX964228.10_*.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 `SRX964228.10_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, 28 Jun 2017 11:15:00: #1 tags after filtering in treatment: 12426352 INFO @ Wed, 28 Jun 2017 11:15:00: #1 tags after filtering in treatment: 12426352 INFO @ Wed, 28 Jun 2017 11:15:00: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 11:15:00: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 11:15:00: #1 finished! INFO @ Wed, 28 Jun 2017 11:15:00: #1 finished! INFO @ Wed, 28 Jun 2017 11:15:00: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 11:15:00: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 11:15:00: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 11:15:00: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 11:15:01: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 11:15:01: 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, 28 Jun 2017 11:15:01: Process for pairing-model is terminated! cat: SRX964228.20_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 `SRX964228.20_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 `SRX964228.20_*.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 `SRX964228.20_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, 28 Jun 2017 11:15:01: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 11:15:01: 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, 28 Jun 2017 11:15:01: Process for pairing-model is terminated! cat: SRX964228.05_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 `SRX964228.05_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 `SRX964228.05_*.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 `SRX964228.05_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。