Job ID = 10937415 sra ファイルのダウンロード中... Completed: 344364K bytes transferred in 6 seconds (454752K 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 4754452 spots for /home/okishinya/chipatlas/results/sacCer3/SRX2198721/SRR4304451.sra Written 4754452 spots for /home/okishinya/chipatlas/results/sacCer3/SRX2198721/SRR4304451.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: 00:05:10 4754452 reads; of these: 4754452 (100.00%) were paired; of these: 1149348 (24.17%) aligned concordantly 0 times 2402190 (50.53%) aligned concordantly exactly 1 time 1202914 (25.30%) aligned concordantly >1 times ---- 1149348 pairs aligned concordantly 0 times; of these: 68200 (5.93%) aligned discordantly 1 time ---- 1081148 pairs aligned 0 times concordantly or discordantly; of these: 2162296 mates make up the pairs; of these: 1995980 (92.31%) aligned 0 times 68620 (3.17%) aligned exactly 1 time 97696 (4.52%) aligned >1 times 79.01% overall alignment rate Time searching: 00:05:10 Overall time: 00:05:10 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] 388525 / 3661250 = 0.1061 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, 10 Aug 2018 02:06:06: # Command line: callpeak -t SRX2198721.bam -f BAM -g 12100000 -n SRX2198721.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX2198721.10 # format = BAM # ChIP-seq file = ['SRX2198721.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, 10 Aug 2018 02:06:06: #1 read tag files... INFO @ Fri, 10 Aug 2018 02:06:06: #1 read treatment tags... INFO @ Fri, 10 Aug 2018 02:06:06: # Command line: callpeak -t SRX2198721.bam -f BAM -g 12100000 -n SRX2198721.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX2198721.20 # format = BAM # ChIP-seq file = ['SRX2198721.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, 10 Aug 2018 02:06:06: #1 read tag files... INFO @ Fri, 10 Aug 2018 02:06:06: #1 read treatment tags... INFO @ Fri, 10 Aug 2018 02:06:06: # Command line: callpeak -t SRX2198721.bam -f BAM -g 12100000 -n SRX2198721.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX2198721.05 # format = BAM # ChIP-seq file = ['SRX2198721.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, 10 Aug 2018 02:06:06: #1 read tag files... INFO @ Fri, 10 Aug 2018 02:06:06: #1 read treatment tags... INFO @ Fri, 10 Aug 2018 02:06:13: 1000000 INFO @ Fri, 10 Aug 2018 02:06:13: 1000000 INFO @ Fri, 10 Aug 2018 02:06:13: 1000000 INFO @ Fri, 10 Aug 2018 02:06:19: 2000000 INFO @ Fri, 10 Aug 2018 02:06:19: 2000000 INFO @ Fri, 10 Aug 2018 02:06:19: 2000000 INFO @ Fri, 10 Aug 2018 02:06:26: 3000000 INFO @ Fri, 10 Aug 2018 02:06:26: 3000000 INFO @ Fri, 10 Aug 2018 02:06:26: 3000000 INFO @ Fri, 10 Aug 2018 02:06:33: 4000000 INFO @ Fri, 10 Aug 2018 02:06:33: 4000000 INFO @ Fri, 10 Aug 2018 02:06:33: 4000000 INFO @ Fri, 10 Aug 2018 02:06:39: 5000000 INFO @ Fri, 10 Aug 2018 02:06:39: 5000000 INFO @ Fri, 10 Aug 2018 02:06:39: 5000000 INFO @ Fri, 10 Aug 2018 02:06:46: 6000000 INFO @ Fri, 10 Aug 2018 02:06:46: 6000000 INFO @ Fri, 10 Aug 2018 02:06:46: 6000000 INFO @ Fri, 10 Aug 2018 02:06:51: #1 tag size is determined as 51 bps INFO @ Fri, 10 Aug 2018 02:06:51: #1 tag size = 51 INFO @ Fri, 10 Aug 2018 02:06:51: #1 total tags in treatment: 3226175 INFO @ Fri, 10 Aug 2018 02:06:51: #1 user defined the maximum tags... INFO @ Fri, 10 Aug 2018 02:06:51: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Aug 2018 02:06:51: #1 tag size is determined as 51 bps INFO @ Fri, 10 Aug 2018 02:06:51: #1 tag size is determined as 51 bps INFO @ Fri, 10 Aug 2018 02:06:51: #1 tag size = 51 INFO @ Fri, 10 Aug 2018 02:06:51: #1 tag size = 51 INFO @ Fri, 10 Aug 2018 02:06:51: #1 total tags in treatment: 3226175 INFO @ Fri, 10 Aug 2018 02:06:51: #1 total tags in treatment: 3226175 INFO @ Fri, 10 Aug 2018 02:06:51: #1 user defined the maximum tags... INFO @ Fri, 10 Aug 2018 02:06:51: #1 user defined the maximum tags... INFO @ Fri, 10 Aug 2018 02:06:51: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Aug 2018 02:06:51: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Aug 2018 02:06:51: #1 tags after filtering in treatment: 2217594 INFO @ Fri, 10 Aug 2018 02:06:51: #1 Redundant rate of treatment: 0.31 INFO @ Fri, 10 Aug 2018 02:06:51: #1 finished! INFO @ Fri, 10 Aug 2018 02:06:51: #2 Build Peak Model... INFO @ Fri, 10 Aug 2018 02:06:51: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Aug 2018 02:06:51: #1 tags after filtering in treatment: 2217594 INFO @ Fri, 10 Aug 2018 02:06:51: #1 tags after filtering in treatment: 2217594 INFO @ Fri, 10 Aug 2018 02:06:51: #1 Redundant rate of treatment: 0.31 INFO @ Fri, 10 Aug 2018 02:06:51: #1 Redundant rate of treatment: 0.31 INFO @ Fri, 10 Aug 2018 02:06:51: #1 finished! INFO @ Fri, 10 Aug 2018 02:06:51: #1 finished! INFO @ Fri, 10 Aug 2018 02:06:51: #2 Build Peak Model... INFO @ Fri, 10 Aug 2018 02:06:51: #2 Build Peak Model... INFO @ Fri, 10 Aug 2018 02:06:51: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Aug 2018 02:06:51: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Aug 2018 02:06:51: #2 number of paired peaks: 37 WARNING @ Fri, 10 Aug 2018 02:06:51: 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 @ Fri, 10 Aug 2018 02:06:51: Process for pairing-model is terminated! INFO @ Fri, 10 Aug 2018 02:06:51: #2 number of paired peaks: 37 WARNING @ Fri, 10 Aug 2018 02:06:51: 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 @ Fri, 10 Aug 2018 02:06:51: Process for pairing-model is terminated! INFO @ Fri, 10 Aug 2018 02:06:51: #2 number of paired peaks: 37 WARNING @ Fri, 10 Aug 2018 02:06:51: 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 @ Fri, 10 Aug 2018 02:06:51: Process for pairing-model is terminated! cat: SRX2198721.05_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: SRX2198721.10_peaks.narrowPeak: そのようなファイルやディレクトリはありません cat: SRX2198721.20_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) pass1 - making usageList (0 chroms): 1 millis rm: cannot remove `SRX2198721.05_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 `SRX2198721.05_*.xls': 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 `SRX2198721.05_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 pass1 - making usageList (0 chroms): 1 millis rm: cannot remove `SRX2198721.10_model.r': そのようなファイルやディレクトリはありません needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX2198721.10_*.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 `SRX2198721.10_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 rm: cannot remove `SRX2198721.20_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 `SRX2198721.20_*.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 `SRX2198721.20_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。