Job ID = 11192837 sra ファイルのダウンロード中... Completed: 396340K bytes transferred in 8 seconds (382510K 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 10404952 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1972005/SRR3946120.sra Written 10404952 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1972005/SRR3946120.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: 00:07:02 10404952 reads; of these: 10404952 (100.00%) were paired; of these: 5345547 (51.38%) aligned concordantly 0 times 4234046 (40.69%) aligned concordantly exactly 1 time 825359 (7.93%) aligned concordantly >1 times ---- 5345547 pairs aligned concordantly 0 times; of these: 35779 (0.67%) aligned discordantly 1 time ---- 5309768 pairs aligned 0 times concordantly or discordantly; of these: 10619536 mates make up the pairs; of these: 6188130 (58.27%) aligned 0 times 3576719 (33.68%) aligned exactly 1 time 854687 (8.05%) aligned >1 times 70.26% overall alignment rate Time searching: 00:07:02 Overall time: 00:07:02 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] 3624292 / 5079638 = 0.7135 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 10:08:59: # Command line: callpeak -t SRX1972005.bam -f BAM -g 12100000 -n SRX1972005.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX1972005.10 # format = BAM # ChIP-seq file = ['SRX1972005.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 10:08:59: #1 read tag files... INFO @ Sat, 15 Sep 2018 10:08:59: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 10:08:59: # Command line: callpeak -t SRX1972005.bam -f BAM -g 12100000 -n SRX1972005.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX1972005.20 # format = BAM # ChIP-seq file = ['SRX1972005.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 10:08:59: #1 read tag files... INFO @ Sat, 15 Sep 2018 10:08:59: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 10:08:59: # Command line: callpeak -t SRX1972005.bam -f BAM -g 12100000 -n SRX1972005.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX1972005.05 # format = BAM # ChIP-seq file = ['SRX1972005.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 10:08:59: #1 read tag files... INFO @ Sat, 15 Sep 2018 10:08:59: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 10:09:05: 1000000 INFO @ Sat, 15 Sep 2018 10:09:05: 1000000 INFO @ Sat, 15 Sep 2018 10:09:05: 1000000 INFO @ Sat, 15 Sep 2018 10:09:10: 2000000 INFO @ Sat, 15 Sep 2018 10:09:10: 2000000 INFO @ Sat, 15 Sep 2018 10:09:10: 2000000 INFO @ Sat, 15 Sep 2018 10:09:16: 3000000 INFO @ Sat, 15 Sep 2018 10:09:16: 3000000 INFO @ Sat, 15 Sep 2018 10:09:16: 3000000 INFO @ Sat, 15 Sep 2018 10:09:21: 4000000 INFO @ Sat, 15 Sep 2018 10:09:22: 4000000 INFO @ Sat, 15 Sep 2018 10:09:22: 4000000 INFO @ Sat, 15 Sep 2018 10:09:27: 5000000 INFO @ Sat, 15 Sep 2018 10:09:27: 5000000 INFO @ Sat, 15 Sep 2018 10:09:27: 5000000 INFO @ Sat, 15 Sep 2018 10:09:33: 6000000 INFO @ Sat, 15 Sep 2018 10:09:33: 6000000 INFO @ Sat, 15 Sep 2018 10:09:33: 6000000 INFO @ Sat, 15 Sep 2018 10:09:38: 7000000 INFO @ Sat, 15 Sep 2018 10:09:38: 7000000 INFO @ Sat, 15 Sep 2018 10:09:38: 7000000 INFO @ Sat, 15 Sep 2018 10:09:40: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 10:09:40: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 10:09:40: #1 total tags in treatment: 1445298 INFO @ Sat, 15 Sep 2018 10:09:40: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 10:09:40: #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 10:09:40: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 10:09:40: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 10:09:40: #1 total tags in treatment: 1445298 INFO @ Sat, 15 Sep 2018 10:09:40: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 10:09:40: #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 10:09:40: #1 tags after filtering in treatment: 1213129 INFO @ Sat, 15 Sep 2018 10:09:40: #1 Redundant rate of treatment: 0.16 INFO @ Sat, 15 Sep 2018 10:09:40: #1 finished! INFO @ Sat, 15 Sep 2018 10:09:40: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 10:09:40: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 10:09:40: #1 tags after filtering in treatment: 1213129 INFO @ Sat, 15 Sep 2018 10:09:40: #1 Redundant rate of treatment: 0.16 INFO @ Sat, 15 Sep 2018 10:09:40: #1 finished! INFO @ Sat, 15 Sep 2018 10:09:40: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 10:09:40: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 10:09:40: #2 number of paired peaks: 37 WARNING @ Sat, 15 Sep 2018 10:09:40: Too few paired peaks (37) 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 10:09:40: Process for pairing-model is terminated! INFO @ Sat, 15 Sep 2018 10:09:40: #2 number of paired peaks: 37 WARNING @ Sat, 15 Sep 2018 10:09:40: Too few paired peaks (37) 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 10:09:40: Process for pairing-model is terminated! cat: SRX1972005.20_peaks.narrowPeakcat: SRX1972005.10_peaks.narrowPeak: そのようなファイルやディレクトリはありません : 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 10:09:40: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 10:09:40: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 10:09:40: #1 total tags in treatment: 1445298 INFO @ Sat, 15 Sep 2018 10:09:40: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 10:09:40: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) pass1 - making usageList (0 chroms): 1 millis pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184)needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX1972005.10_model.r'rm: : そのようなファイルやディレクトリはありませんcannot remove `SRX1972005.20_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 `SRX1972005.10_*.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 `SRX1972005.20_*.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 `SRX1972005.10_peaks.narrowPeak': そのようなファイルやディレクトリはありません rm: cannot remove `SRX1972005.20_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 CompletedMACS2peakCalling INFO @ Sat, 15 Sep 2018 10:09:40: #1 tags after filtering in treatment: 1213129 INFO @ Sat, 15 Sep 2018 10:09:40: #1 Redundant rate of treatment: 0.16 INFO @ Sat, 15 Sep 2018 10:09:40: #1 finished! INFO @ Sat, 15 Sep 2018 10:09:40: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 10:09:40: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 10:09:40: #2 number of paired peaks: 37 WARNING @ Sat, 15 Sep 2018 10:09:40: Too few paired peaks (37) 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 10:09:40: Process for pairing-model is terminated! cat: SRX1972005.05_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 `SRX1972005.05_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 `SRX1972005.05_*.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 `SRX1972005.05_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。