Job ID = 11245244 sra ファイルのダウンロード中... Completed: 380665K bytes transferred in 6 seconds (482127K 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 8942616 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4733454/SRR7896009.sra Written 8942616 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4733454/SRR7896009.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: 00:01:54 8942616 reads; of these: 8942616 (100.00%) were unpaired; of these: 2623129 (29.33%) aligned 0 times 3707559 (41.46%) aligned exactly 1 time 2611928 (29.21%) aligned >1 times 70.67% overall alignment rate Time searching: 00:01:54 Overall time: 00:01:54 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] 4983690 / 6319487 = 0.7886 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, 10 Oct 2018 00:05:56: # Command line: callpeak -t SRX4733454.bam -f BAM -g 12100000 -n SRX4733454.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX4733454.05 # format = BAM # ChIP-seq file = ['SRX4733454.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, 10 Oct 2018 00:05:56: #1 read tag files... INFO @ Wed, 10 Oct 2018 00:05:56: #1 read treatment tags... INFO @ Wed, 10 Oct 2018 00:05:56: # Command line: callpeak -t SRX4733454.bam -f BAM -g 12100000 -n SRX4733454.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX4733454.20 # format = BAM # ChIP-seq file = ['SRX4733454.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, 10 Oct 2018 00:05:56: #1 read tag files... INFO @ Wed, 10 Oct 2018 00:05:56: #1 read treatment tags... INFO @ Wed, 10 Oct 2018 00:05:56: # Command line: callpeak -t SRX4733454.bam -f BAM -g 12100000 -n SRX4733454.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX4733454.10 # format = BAM # ChIP-seq file = ['SRX4733454.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, 10 Oct 2018 00:05:56: #1 read tag files... INFO @ Wed, 10 Oct 2018 00:05:56: #1 read treatment tags... INFO @ Wed, 10 Oct 2018 00:06:04: 1000000 INFO @ Wed, 10 Oct 2018 00:06:04: 1000000 INFO @ Wed, 10 Oct 2018 00:06:04: 1000000 INFO @ Wed, 10 Oct 2018 00:06:07: #1 tag size is determined as 101 bps INFO @ Wed, 10 Oct 2018 00:06:07: #1 tag size = 101 INFO @ Wed, 10 Oct 2018 00:06:07: #1 total tags in treatment: 1335797 INFO @ Wed, 10 Oct 2018 00:06:07: #1 user defined the maximum tags... INFO @ Wed, 10 Oct 2018 00:06:07: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 10 Oct 2018 00:06:07: #1 tag size is determined as 101 bps INFO @ Wed, 10 Oct 2018 00:06:07: #1 tag size = 101 INFO @ Wed, 10 Oct 2018 00:06:07: #1 total tags in treatment: 1335797 INFO @ Wed, 10 Oct 2018 00:06:07: #1 user defined the maximum tags... INFO @ Wed, 10 Oct 2018 00:06:07: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 10 Oct 2018 00:06:07: #1 tag size is determined as 101 bps INFO @ Wed, 10 Oct 2018 00:06:07: #1 tag size = 101 INFO @ Wed, 10 Oct 2018 00:06:07: #1 total tags in treatment: 1335797 INFO @ Wed, 10 Oct 2018 00:06:07: #1 user defined the maximum tags... INFO @ Wed, 10 Oct 2018 00:06:07: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 10 Oct 2018 00:06:07: #1 tags after filtering in treatment: 1335797 INFO @ Wed, 10 Oct 2018 00:06:07: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 10 Oct 2018 00:06:07: #1 finished! INFO @ Wed, 10 Oct 2018 00:06:07: #2 Build Peak Model... INFO @ Wed, 10 Oct 2018 00:06:07: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 10 Oct 2018 00:06:07: #1 tags after filtering in treatment: 1335797 INFO @ Wed, 10 Oct 2018 00:06:07: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 10 Oct 2018 00:06:07: #1 finished! INFO @ Wed, 10 Oct 2018 00:06:07: #2 Build Peak Model... INFO @ Wed, 10 Oct 2018 00:06:07: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 10 Oct 2018 00:06:07: #1 tags after filtering in treatment: 1335797 INFO @ Wed, 10 Oct 2018 00:06:07: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 10 Oct 2018 00:06:07: #1 finished! INFO @ Wed, 10 Oct 2018 00:06:07: #2 Build Peak Model... INFO @ Wed, 10 Oct 2018 00:06:07: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 10 Oct 2018 00:06:07: #2 number of paired peaks: 30 WARNING @ Wed, 10 Oct 2018 00:06:07: Too few paired peaks (30) 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, 10 Oct 2018 00:06:07: Process for pairing-model is terminated! cat: SRX4733454.10_peaks.narrowPeak: そのようなファイルやディレクトリはありません INFO @ Wed, 10 Oct 2018 00:06:07: #2 number of paired peaks: 30 WARNING @ Wed, 10 Oct 2018 00:06:07: Too few paired peaks (30) 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, 10 Oct 2018 00:06:07: Process for pairing-model is terminated! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4733454.10_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 `SRX4733454.10_*.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 `SRX4733454.10_peaks.narrowPeak': そのようなファイルやディレクトリはありません INFO @ Wed, 10 Oct 2018 00:06:07: #2 number of paired peaks: 30 cat: CompletedMACS2peakCalling SRX4733454.20_peaks.narrowPeakWARNING @ Wed, 10 Oct 2018 00:06:07: Too few paired peaks (30) 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, 10 Oct 2018 00:06:07: Process for pairing-model is terminated! : 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 cat: SRX4733454.05_peaks.narrowPeak: そのようなファイルやディレクトリはありません needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4733454.20_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 `SRX4733454.20_*.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 `SRX4733454.20_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 pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4733454.05_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 `SRX4733454.05_*.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 `SRX4733454.05_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。