Job ID = 11245062 sra ファイルのダウンロード中... Completed: 153901K bytes transferred in 4 seconds (257459K 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 5321523 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4554775/SRR7696447.sra Written 5321523 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4554775/SRR7696447.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: 00:02:59 5321523 reads; of these: 5321523 (100.00%) were paired; of these: 2840018 (53.37%) aligned concordantly 0 times 2250820 (42.30%) aligned concordantly exactly 1 time 230685 (4.33%) aligned concordantly >1 times ---- 2840018 pairs aligned concordantly 0 times; of these: 54002 (1.90%) aligned discordantly 1 time ---- 2786016 pairs aligned 0 times concordantly or discordantly; of these: 5572032 mates make up the pairs; of these: 3482252 (62.50%) aligned 0 times 1874362 (33.64%) aligned exactly 1 time 215418 (3.87%) aligned >1 times 67.28% overall alignment rate Time searching: 00:02:59 Overall time: 00:02:59 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] 110990 / 2534967 = 0.0438 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 @ Tue, 09 Oct 2018 23:21:25: # Command line: callpeak -t SRX4554775.bam -f BAM -g 12100000 -n SRX4554775.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX4554775.10 # format = BAM # ChIP-seq file = ['SRX4554775.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 @ Tue, 09 Oct 2018 23:21:25: #1 read tag files... INFO @ Tue, 09 Oct 2018 23:21:25: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 23:21:25: # Command line: callpeak -t SRX4554775.bam -f BAM -g 12100000 -n SRX4554775.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX4554775.05 # format = BAM # ChIP-seq file = ['SRX4554775.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 @ Tue, 09 Oct 2018 23:21:25: #1 read tag files... INFO @ Tue, 09 Oct 2018 23:21:25: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 23:21:25: # Command line: callpeak -t SRX4554775.bam -f BAM -g 12100000 -n SRX4554775.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX4554775.20 # format = BAM # ChIP-seq file = ['SRX4554775.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 @ Tue, 09 Oct 2018 23:21:25: #1 read tag files... INFO @ Tue, 09 Oct 2018 23:21:25: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 23:21:31: 1000000 INFO @ Tue, 09 Oct 2018 23:21:31: 1000000 INFO @ Tue, 09 Oct 2018 23:21:31: 1000000 INFO @ Tue, 09 Oct 2018 23:21:37: 2000000 INFO @ Tue, 09 Oct 2018 23:21:37: 2000000 INFO @ Tue, 09 Oct 2018 23:21:37: 2000000 INFO @ Tue, 09 Oct 2018 23:21:43: 3000000 INFO @ Tue, 09 Oct 2018 23:21:43: 3000000 INFO @ Tue, 09 Oct 2018 23:21:43: 3000000 INFO @ Tue, 09 Oct 2018 23:21:49: 4000000 INFO @ Tue, 09 Oct 2018 23:21:49: 4000000 INFO @ Tue, 09 Oct 2018 23:21:49: 4000000 INFO @ Tue, 09 Oct 2018 23:21:55: 5000000 INFO @ Tue, 09 Oct 2018 23:21:55: 5000000 INFO @ Tue, 09 Oct 2018 23:21:55: 5000000 INFO @ Tue, 09 Oct 2018 23:22:01: 6000000 INFO @ Tue, 09 Oct 2018 23:22:01: 6000000 INFO @ Tue, 09 Oct 2018 23:22:01: 6000000 INFO @ Tue, 09 Oct 2018 23:22:06: #1 tag size is determined as 37 bps INFO @ Tue, 09 Oct 2018 23:22:06: #1 tag size = 37 INFO @ Tue, 09 Oct 2018 23:22:06: #1 total tags in treatment: 2371159 INFO @ Tue, 09 Oct 2018 23:22:06: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 23:22:06: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 09 Oct 2018 23:22:06: #1 tag size is determined as 37 bps INFO @ Tue, 09 Oct 2018 23:22:06: #1 tag size = 37 INFO @ Tue, 09 Oct 2018 23:22:06: #1 total tags in treatment: 2371159 INFO @ Tue, 09 Oct 2018 23:22:06: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 23:22:06: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 09 Oct 2018 23:22:06: #1 tag size is determined as 37 bps INFO @ Tue, 09 Oct 2018 23:22:06: #1 tag size = 37 INFO @ Tue, 09 Oct 2018 23:22:06: #1 total tags in treatment: 2371159 INFO @ Tue, 09 Oct 2018 23:22:06: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 23:22:06: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 09 Oct 2018 23:22:06: #1 tags after filtering in treatment: 1778169 INFO @ Tue, 09 Oct 2018 23:22:06: #1 Redundant rate of treatment: 0.25 INFO @ Tue, 09 Oct 2018 23:22:06: #1 finished! INFO @ Tue, 09 Oct 2018 23:22:06: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 23:22:06: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 23:22:06: #1 tags after filtering in treatment: 1778169 INFO @ Tue, 09 Oct 2018 23:22:06: #1 Redundant rate of treatment: 0.25 INFO @ Tue, 09 Oct 2018 23:22:06: #1 finished! INFO @ Tue, 09 Oct 2018 23:22:06: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 23:22:06: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 23:22:06: #1 tags after filtering in treatment: 1778169 INFO @ Tue, 09 Oct 2018 23:22:06: #1 Redundant rate of treatment: 0.25 INFO @ Tue, 09 Oct 2018 23:22:06: #1 finished! INFO @ Tue, 09 Oct 2018 23:22:06: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 23:22:06: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 23:22:06: #2 number of paired peaks: 14 WARNING @ Tue, 09 Oct 2018 23:22:06: Too few paired peaks (14) 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 @ Tue, 09 Oct 2018 23:22:06: Process for pairing-model is terminated! INFO @ Tue, 09 Oct 2018 23:22:06: #2 number of paired peaks: 14 WARNING @ Tue, 09 Oct 2018 23:22:06: Too few paired peaks (14) 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 @ Tue, 09 Oct 2018 23:22:06: Process for pairing-model is terminated! cat: SRX4554775.10_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)cat: : 1 millis SRX4554775.05_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 `SRX4554775.10_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 `SRX4554775.10_*.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 `SRX4554775.10_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 `SRX4554775.05_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 `SRX4554775.05_*.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 `SRX4554775.05_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 @ Tue, 09 Oct 2018 23:22:06: #2 number of paired peaks: 14 WARNING @ Tue, 09 Oct 2018 23:22:06: Too few paired peaks (14) 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 @ Tue, 09 Oct 2018 23:22:06: Process for pairing-model is terminated! cat: SRX4554775.20_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) rm: cannot remove `SRX4554775.20_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 `SRX4554775.20_*.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 `SRX4554775.20_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。