Job ID = 11193226 sra ファイルのダウンロード中... Completed: 155605K bytes transferred in 4 seconds (283995K 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: PAIRED fastq に変換中... Read 3685206 spots for /home/okishinya/chipatlas/results/sacCer3/SRX977512/SRR1951358.sra Written 3685206 spots for /home/okishinya/chipatlas/results/sacCer3/SRX977512/SRR1951358.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: 00:00:42 3685206 reads; of these: 3685206 (100.00%) were paired; of these: 3158463 (85.71%) aligned concordantly 0 times 446369 (12.11%) aligned concordantly exactly 1 time 80374 (2.18%) aligned concordantly >1 times ---- 3158463 pairs aligned concordantly 0 times; of these: 20704 (0.66%) aligned discordantly 1 time ---- 3137759 pairs aligned 0 times concordantly or discordantly; of these: 6275518 mates make up the pairs; of these: 6230383 (99.28%) aligned 0 times 31068 (0.50%) aligned exactly 1 time 14067 (0.22%) aligned >1 times 15.47% overall alignment rate Time searching: 00:00:42 Overall time: 00:00:42 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_rmdup_core] processing reference chrI... [bam_rmdup_core] processing reference chrII... [bam_rmdup_core] processing reference chrIII... [bam_rmdup_core] processing reference chrIV... [bam_rmdup_core] processing reference chrIX... [bam_rmdup_core] processing reference chrM... [bam_rmdup_core] processing reference chrV... [bam_rmdup_core] processing reference chrVI... [bam_rmdup_core] processing reference chrVII... [bam_rmdup_core] processing reference chrVIII... [bam_rmdup_core] processing reference chrX... [bam_rmdup_core] processing reference chrXI... [bam_rmdup_core] processing reference chrXII... [bam_rmdup_core] processing reference chrXIII... [bam_rmdup_core] processing reference chrXIV... [bam_rmdup_core] processing reference chrXV... [bam_rmdup_core] processing reference chrXVI... [bam_rmdup_core] 207146 / 542462 = 0.3819 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 @ Sat, 15 Sep 2018 11:14:18: # Command line: callpeak -t SRX977512.bam -f BAM -g 12100000 -n SRX977512.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX977512.10 # format = BAM # ChIP-seq file = ['SRX977512.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 @ Sat, 15 Sep 2018 11:14:18: # Command line: callpeak -t SRX977512.bam -f BAM -g 12100000 -n SRX977512.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX977512.20 # format = BAM # ChIP-seq file = ['SRX977512.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 @ Sat, 15 Sep 2018 11:14:18: # Command line: callpeak -t SRX977512.bam -f BAM -g 12100000 -n SRX977512.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX977512.05 # format = BAM # ChIP-seq file = ['SRX977512.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 @ Sat, 15 Sep 2018 11:14:18: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:14:18: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:14:18: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:14:18: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:14:18: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:14:18: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:14:23: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 11:14:23: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 11:14:23: #1 total tags in treatment: 327014 INFO @ Sat, 15 Sep 2018 11:14:23: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:14:23: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 11:14:23: #1 tags after filtering in treatment: 308918 INFO @ Sat, 15 Sep 2018 11:14:23: #1 Redundant rate of treatment: 0.06 INFO @ Sat, 15 Sep 2018 11:14:23: #1 finished! INFO @ Sat, 15 Sep 2018 11:14:23: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:14:23: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:14:23: #2 number of paired peaks: 38 WARNING @ Sat, 15 Sep 2018 11:14:23: Too few paired peaks (38) 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 @ Sat, 15 Sep 2018 11:14:23: Process for pairing-model is terminated! cat: SRX977512.05_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): 0 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX977512.05_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 `SRX977512.05_*.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 `SRX977512.05_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 @ Sat, 15 Sep 2018 11:14:23: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 11:14:23: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 11:14:23: #1 total tags in treatment: 327014 INFO @ Sat, 15 Sep 2018 11:14:23: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:14:23: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 11:14:23: #1 tags after filtering in treatment: 308918 INFO @ Sat, 15 Sep 2018 11:14:23: #1 Redundant rate of treatment: 0.06 INFO @ Sat, 15 Sep 2018 11:14:23: #1 finished! INFO @ Sat, 15 Sep 2018 11:14:23: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:14:23: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:14:23: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 11:14:23: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 11:14:23: #1 total tags in treatment: 327014 INFO @ Sat, 15 Sep 2018 11:14:23: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:14:23: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 11:14:23: #1 tags after filtering in treatment: 308918 INFO @ Sat, 15 Sep 2018 11:14:23: #1 Redundant rate of treatment: 0.06 INFO @ Sat, 15 Sep 2018 11:14:23: #1 finished! INFO @ Sat, 15 Sep 2018 11:14:23: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:14:23: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:14:23: #2 number of paired peaks: 38 WARNING @ Sat, 15 Sep 2018 11:14:23: Too few paired peaks (38) 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 @ Sat, 15 Sep 2018 11:14:23: Process for pairing-model is terminated! cat: SRX977512.10_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 @ Sat, 15 Sep 2018 11:14:23: #2 number of paired peaks: 38 WARNING @ Sat, 15 Sep 2018 11:14:23: Too few paired peaks (38) 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 @ Sat, 15 Sep 2018 11:14:23: Process for pairing-model is terminated! pass1 - making usageList (0 chroms): 0 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX977512.10_model.r': そのようなファイルやディレクトリはありません cat: SRX977512.20_peaks.narrowPeakrm: cannot remove `SRX977512.10_*.xls': 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 `SRX977512.10_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 pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX977512.20_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 `SRX977512.20_*.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 `SRX977512.20_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 BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。