Job ID = 11634639 sra ファイルのダウンロード中... Completed: 288089K bytes transferred in 5 seconds (403251K 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 10029585 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3933752/SRR7000950.sra Written 10029585 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3933752/SRR7000950.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: 00:02:25 10029585 reads; of these: 10029585 (100.00%) were unpaired; of these: 891238 (8.89%) aligned 0 times 8139180 (81.15%) aligned exactly 1 time 999167 (9.96%) aligned >1 times 91.11% overall alignment rate Time searching: 00:02:25 Overall time: 00:02:25 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] 4494933 / 9138347 = 0.4919 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 @ Fri, 15 Feb 2019 10:23:10: # Command line: callpeak -t SRX3933752.bam -f BAM -g 12100000 -n SRX3933752.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3933752.10 # format = BAM # ChIP-seq file = ['SRX3933752.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 @ Fri, 15 Feb 2019 10:23:10: #1 read tag files... INFO @ Fri, 15 Feb 2019 10:23:10: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 10:23:10: # Command line: callpeak -t SRX3933752.bam -f BAM -g 12100000 -n SRX3933752.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3933752.05 # format = BAM # ChIP-seq file = ['SRX3933752.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 @ Fri, 15 Feb 2019 10:23:10: #1 read tag files... INFO @ Fri, 15 Feb 2019 10:23:10: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 10:23:10: # Command line: callpeak -t SRX3933752.bam -f BAM -g 12100000 -n SRX3933752.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3933752.20 # format = BAM # ChIP-seq file = ['SRX3933752.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 @ Fri, 15 Feb 2019 10:23:10: #1 read tag files... INFO @ Fri, 15 Feb 2019 10:23:10: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 10:23:17: 1000000 INFO @ Fri, 15 Feb 2019 10:23:18: 1000000 INFO @ Fri, 15 Feb 2019 10:23:18: 1000000 INFO @ Fri, 15 Feb 2019 10:23:25: 2000000 INFO @ Fri, 15 Feb 2019 10:23:25: 2000000 INFO @ Fri, 15 Feb 2019 10:23:25: 2000000 INFO @ Fri, 15 Feb 2019 10:23:33: 3000000 INFO @ Fri, 15 Feb 2019 10:23:33: 3000000 INFO @ Fri, 15 Feb 2019 10:23:33: 3000000 INFO @ Fri, 15 Feb 2019 10:23:41: 4000000 INFO @ Fri, 15 Feb 2019 10:23:41: 4000000 INFO @ Fri, 15 Feb 2019 10:23:41: 4000000 INFO @ Fri, 15 Feb 2019 10:23:45: #1 tag size is determined as 75 bps INFO @ Fri, 15 Feb 2019 10:23:45: #1 tag size = 75 INFO @ Fri, 15 Feb 2019 10:23:45: #1 total tags in treatment: 4643414 INFO @ Fri, 15 Feb 2019 10:23:45: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 10:23:45: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 10:23:45: #1 tags after filtering in treatment: 4643414 INFO @ Fri, 15 Feb 2019 10:23:45: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 10:23:45: #1 finished! INFO @ Fri, 15 Feb 2019 10:23:45: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 10:23:45: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 10:23:46: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 10:23:46: 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 @ Fri, 15 Feb 2019 10:23:46: Process for pairing-model is terminated! cat: SRX3933752.10_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): 3 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX3933752.10_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 `SRX3933752.10_*.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 `SRX3933752.10_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 @ Fri, 15 Feb 2019 10:23:46: #1 tag size is determined as 75 bps INFO @ Fri, 15 Feb 2019 10:23:46: #1 tag size = 75 INFO @ Fri, 15 Feb 2019 10:23:46: #1 total tags in treatment: 4643414 INFO @ Fri, 15 Feb 2019 10:23:46: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 10:23:46: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 10:23:46: #1 tag size is determined as 75 bps INFO @ Fri, 15 Feb 2019 10:23:46: #1 tag size = 75 INFO @ Fri, 15 Feb 2019 10:23:46: #1 total tags in treatment: 4643414 INFO @ Fri, 15 Feb 2019 10:23:46: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 10:23:46: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 10:23:46: #1 tags after filtering in treatment: 4643414 INFO @ Fri, 15 Feb 2019 10:23:46: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 10:23:46: #1 finished! INFO @ Fri, 15 Feb 2019 10:23:46: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 10:23:46: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 10:23:46: #1 tags after filtering in treatment: 4643414 INFO @ Fri, 15 Feb 2019 10:23:46: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 10:23:46: #1 finished! INFO @ Fri, 15 Feb 2019 10:23:46: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 10:23:46: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 10:23:46: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 10:23:46: 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 @ Fri, 15 Feb 2019 10:23:46: Process for pairing-model is terminated! cat: SRX3933752.20_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): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX3933752.20_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 `SRX3933752.20_*.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 `SRX3933752.20_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 @ Fri, 15 Feb 2019 10:23:46: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 10:23:46: 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 @ Fri, 15 Feb 2019 10:23:46: Process for pairing-model is terminated! cat: SRX3933752.05_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): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX3933752.05_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 `SRX3933752.05_*.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 `SRX3933752.05_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。