Job ID = 11192667 sra ファイルのダウンロード中... Completed: 16523K bytes transferred in 2 seconds (46901K 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 536615 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1924788/SRR3824819.sra Written 536615 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1924788/SRR3824819.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: 00:00:22 536615 reads; of these: 536615 (100.00%) were paired; of these: 168624 (31.42%) aligned concordantly 0 times 340657 (63.48%) aligned concordantly exactly 1 time 27334 (5.09%) aligned concordantly >1 times ---- 168624 pairs aligned concordantly 0 times; of these: 38730 (22.97%) aligned discordantly 1 time ---- 129894 pairs aligned 0 times concordantly or discordantly; of these: 259788 mates make up the pairs; of these: 133343 (51.33%) aligned 0 times 111484 (42.91%) aligned exactly 1 time 14961 (5.76%) aligned >1 times 87.58% overall alignment rate Time searching: 00:00:22 Overall time: 00:00:22 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 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] 153474 / 385839 = 0.3978 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 09:44:12: # Command line: callpeak -t SRX1924788.bam -f BAM -g 12100000 -n SRX1924788.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX1924788.10 # format = BAM # ChIP-seq file = ['SRX1924788.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 09:44:12: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:44:12: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:44:12: # Command line: callpeak -t SRX1924788.bam -f BAM -g 12100000 -n SRX1924788.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX1924788.05 # format = BAM # ChIP-seq file = ['SRX1924788.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 09:44:12: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:44:12: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:44:12: # Command line: callpeak -t SRX1924788.bam -f BAM -g 12100000 -n SRX1924788.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX1924788.20 # format = BAM # ChIP-seq file = ['SRX1924788.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 09:44:12: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:44:12: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:44:15: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 09:44:15: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 09:44:15: #1 total tags in treatment: 219853 INFO @ Sat, 15 Sep 2018 09:44:15: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:44:15: #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 09:44:15: #1 tags after filtering in treatment: 212601 INFO @ Sat, 15 Sep 2018 09:44:15: #1 Redundant rate of treatment: 0.03 INFO @ Sat, 15 Sep 2018 09:44:15: #1 finished! INFO @ Sat, 15 Sep 2018 09:44:15: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:44:15: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:44:15: #2 number of paired peaks: 34 WARNING @ Sat, 15 Sep 2018 09:44:15: Too few paired peaks (34) 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 09:44:15: Process for pairing-model is terminated! cat: SRX1924788.10_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 `SRX1924788.10_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 `SRX1924788.10_*.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 `SRX1924788.10_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 @ Sat, 15 Sep 2018 09:44:15: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 09:44:15: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 09:44:15: #1 total tags in treatment: 219853 INFO @ Sat, 15 Sep 2018 09:44:15: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:44:15: #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 09:44:15: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 09:44:15: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 09:44:15: #1 total tags in treatment: 219853 INFO @ Sat, 15 Sep 2018 09:44:15: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:44:15: #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 09:44:15: #1 tags after filtering in treatment: 212601 INFO @ Sat, 15 Sep 2018 09:44:15: #1 Redundant rate of treatment: 0.03 INFO @ Sat, 15 Sep 2018 09:44:15: #1 finished! INFO @ Sat, 15 Sep 2018 09:44:15: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:44:15: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:44:15: #1 tags after filtering in treatment: 212601 INFO @ Sat, 15 Sep 2018 09:44:15: #1 Redundant rate of treatment: 0.03 INFO @ Sat, 15 Sep 2018 09:44:15: #1 finished! INFO @ Sat, 15 Sep 2018 09:44:15: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:44:15: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:44:15: #2 number of paired peaks: 34 WARNING @ Sat, 15 Sep 2018 09:44:15: Too few paired peaks (34) 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 09:44:15: Process for pairing-model is terminated! INFO @ Sat, 15 Sep 2018 09:44:15: #2 number of paired peaks: 34 WARNING @ Sat, 15 Sep 2018 09:44:15: Too few paired peaks (34) 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 09:44:15: Process for pairing-model is terminated! cat: SRX1924788.05_peaks.narrowPeak: そのようなファイルやディレクトリはありません cat: SRX1924788.20_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) pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX1924788.05_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 `SRX1924788.05_*.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 `SRX1924788.05_peaks.narrowPeak': そのようなファイルやディレクトリはありません rm: cannot remove `SRX1924788.20_model.r': そのようなファイルやディレクトリはありません CompletedMACS2peakCalling rm: cannot remove `SRX1924788.20_*.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 `SRX1924788.20_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。