Job ID = 10254449 sra ファイルのダウンロード中... Completed: 170768K bytes transferred in 6 seconds (206212K bits/sec), in 1 file. Completed: 202085K bytes transferred in 9 seconds (174038K 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... Written 6765760 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3353387/SRR6246248.sra Written 6765760 spots total Written 8006374 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3353387/SRR6246249.sra Written 8006374 spots total 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 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: 00:02:12 14772134 reads; of these: 14772134 (100.00%) were unpaired; of these: 4795228 (32.46%) aligned 0 times 9350879 (63.30%) aligned exactly 1 time 626027 (4.24%) aligned >1 times 67.54% overall alignment rate Time searching: 00:02:12 Overall time: 00:02:12 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 8 files... [bam_rmdupse_core] 3435052 / 9976906 = 0.3443 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, 06 Dec 2017 18:14:42: # Command line: callpeak -t SRX3353387.bam -f BAM -g 12100000 -n SRX3353387.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3353387.10 # format = BAM # ChIP-seq file = ['SRX3353387.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, 06 Dec 2017 18:14:42: #1 read tag files... INFO @ Wed, 06 Dec 2017 18:14:42: #1 read treatment tags... INFO @ Wed, 06 Dec 2017 18:14:42: # Command line: callpeak -t SRX3353387.bam -f BAM -g 12100000 -n SRX3353387.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3353387.05 # format = BAM # ChIP-seq file = ['SRX3353387.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, 06 Dec 2017 18:14:42: #1 read tag files... INFO @ Wed, 06 Dec 2017 18:14:42: #1 read treatment tags... INFO @ Wed, 06 Dec 2017 18:14:42: # Command line: callpeak -t SRX3353387.bam -f BAM -g 12100000 -n SRX3353387.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3353387.20 # format = BAM # ChIP-seq file = ['SRX3353387.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, 06 Dec 2017 18:14:42: #1 read tag files... INFO @ Wed, 06 Dec 2017 18:14:42: #1 read treatment tags... INFO @ Wed, 06 Dec 2017 18:14:48: 1000000 INFO @ Wed, 06 Dec 2017 18:14:49: 1000000 INFO @ Wed, 06 Dec 2017 18:14:49: 1000000 INFO @ Wed, 06 Dec 2017 18:14:55: 2000000 INFO @ Wed, 06 Dec 2017 18:14:56: 2000000 INFO @ Wed, 06 Dec 2017 18:14:56: 2000000 INFO @ Wed, 06 Dec 2017 18:15:02: 3000000 INFO @ Wed, 06 Dec 2017 18:15:03: 3000000 INFO @ Wed, 06 Dec 2017 18:15:03: 3000000 INFO @ Wed, 06 Dec 2017 18:15:09: 4000000 INFO @ Wed, 06 Dec 2017 18:15:09: 4000000 INFO @ Wed, 06 Dec 2017 18:15:10: 4000000 INFO @ Wed, 06 Dec 2017 18:15:16: 5000000 INFO @ Wed, 06 Dec 2017 18:15:16: 5000000 INFO @ Wed, 06 Dec 2017 18:15:17: 5000000 INFO @ Wed, 06 Dec 2017 18:15:23: 6000000 INFO @ Wed, 06 Dec 2017 18:15:23: 6000000 INFO @ Wed, 06 Dec 2017 18:15:25: 6000000 INFO @ Wed, 06 Dec 2017 18:15:27: #1 tag size is determined as 51 bps INFO @ Wed, 06 Dec 2017 18:15:27: #1 tag size = 51 INFO @ Wed, 06 Dec 2017 18:15:27: #1 total tags in treatment: 6541854 INFO @ Wed, 06 Dec 2017 18:15:27: #1 user defined the maximum tags... INFO @ Wed, 06 Dec 2017 18:15:27: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 06 Dec 2017 18:15:27: #1 tag size is determined as 51 bps INFO @ Wed, 06 Dec 2017 18:15:27: #1 tag size = 51 INFO @ Wed, 06 Dec 2017 18:15:27: #1 total tags in treatment: 6541854 INFO @ Wed, 06 Dec 2017 18:15:27: #1 user defined the maximum tags... INFO @ Wed, 06 Dec 2017 18:15:27: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 06 Dec 2017 18:15:27: #1 tags after filtering in treatment: 6541854 INFO @ Wed, 06 Dec 2017 18:15:27: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 06 Dec 2017 18:15:27: #1 finished! INFO @ Wed, 06 Dec 2017 18:15:27: #2 Build Peak Model... INFO @ Wed, 06 Dec 2017 18:15:27: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 06 Dec 2017 18:15:27: #1 tags after filtering in treatment: 6541854 INFO @ Wed, 06 Dec 2017 18:15:27: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 06 Dec 2017 18:15:27: #1 finished! INFO @ Wed, 06 Dec 2017 18:15:27: #2 Build Peak Model... INFO @ Wed, 06 Dec 2017 18:15:27: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 06 Dec 2017 18:15:27: #2 number of paired peaks: 0 WARNING @ Wed, 06 Dec 2017 18:15:27: 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, 06 Dec 2017 18:15:27: Process for pairing-model is terminated! cat: SRX3353387.20_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 `SRX3353387.20_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 `SRX3353387.20_*.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 `SRX3353387.20_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, 06 Dec 2017 18:15:27: #2 number of paired peaks: 0 WARNING @ Wed, 06 Dec 2017 18:15:27: 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, 06 Dec 2017 18:15:27: Process for pairing-model is terminated! cat: SRX3353387.05_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 `SRX3353387.05_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 `SRX3353387.05_*.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 `SRX3353387.05_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 INFO @ Wed, 06 Dec 2017 18:15:28: #1 tag size is determined as 51 bps INFO @ Wed, 06 Dec 2017 18:15:28: #1 tag size = 51 INFO @ Wed, 06 Dec 2017 18:15:28: #1 total tags in treatment: 6541854 INFO @ Wed, 06 Dec 2017 18:15:28: #1 user defined the maximum tags... INFO @ Wed, 06 Dec 2017 18:15:28: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 06 Dec 2017 18:15:28: #1 tags after filtering in treatment: 6541854 INFO @ Wed, 06 Dec 2017 18:15:28: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 06 Dec 2017 18:15:28: #1 finished! INFO @ Wed, 06 Dec 2017 18:15:28: #2 Build Peak Model... INFO @ Wed, 06 Dec 2017 18:15:28: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 06 Dec 2017 18:15:29: #2 number of paired peaks: 0 WARNING @ Wed, 06 Dec 2017 18:15:29: 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, 06 Dec 2017 18:15:29: Process for pairing-model is terminated! cat: SRX3353387.10_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 `SRX3353387.10_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 `SRX3353387.10_*.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 `SRX3353387.10_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。