Job ID = 10609016 sra ファイルのダウンロード中... Completed: 192089K bytes transferred in 7 seconds (203659K 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... Written 1967905 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3063103/SRR5901533.sra Written 1967905 spots total 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: 00:02:31 1967905 reads; of these: 1967905 (100.00%) were paired; of these: 111287 (5.66%) aligned concordantly 0 times 1566220 (79.59%) aligned concordantly exactly 1 time 290398 (14.76%) aligned concordantly >1 times ---- 111287 pairs aligned concordantly 0 times; of these: 41856 (37.61%) aligned discordantly 1 time ---- 69431 pairs aligned 0 times concordantly or discordantly; of these: 138862 mates make up the pairs; of these: 78007 (56.18%) aligned 0 times 38793 (27.94%) aligned exactly 1 time 22062 (15.89%) aligned >1 times 98.02% overall alignment rate Time searching: 00:02:31 Overall time: 00:02:31 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] 38847 / 1876251 = 0.0207 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 @ Thu, 03 May 2018 23:11:30: # Command line: callpeak -t SRX3063103.bam -f BAM -g 12100000 -n SRX3063103.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3063103.05 # format = BAM # ChIP-seq file = ['SRX3063103.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 @ Thu, 03 May 2018 23:11:30: #1 read tag files... INFO @ Thu, 03 May 2018 23:11:30: #1 read treatment tags... INFO @ Thu, 03 May 2018 23:11:30: # Command line: callpeak -t SRX3063103.bam -f BAM -g 12100000 -n SRX3063103.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3063103.10 # format = BAM # ChIP-seq file = ['SRX3063103.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 @ Thu, 03 May 2018 23:11:30: #1 read tag files... INFO @ Thu, 03 May 2018 23:11:30: #1 read treatment tags... INFO @ Thu, 03 May 2018 23:11:30: # Command line: callpeak -t SRX3063103.bam -f BAM -g 12100000 -n SRX3063103.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3063103.20 # format = BAM # ChIP-seq file = ['SRX3063103.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 @ Thu, 03 May 2018 23:11:30: #1 read tag files... INFO @ Thu, 03 May 2018 23:11:30: #1 read treatment tags... INFO @ Thu, 03 May 2018 23:11:39: 1000000 INFO @ Thu, 03 May 2018 23:11:39: 1000000 INFO @ Thu, 03 May 2018 23:11:39: 1000000 INFO @ Thu, 03 May 2018 23:11:48: 2000000 INFO @ Thu, 03 May 2018 23:11:50: 2000000 INFO @ Thu, 03 May 2018 23:11:50: 2000000 INFO @ Thu, 03 May 2018 23:11:56: 3000000 INFO @ Thu, 03 May 2018 23:11:59: 3000000 INFO @ Thu, 03 May 2018 23:11:59: 3000000 INFO @ Thu, 03 May 2018 23:12:02: #1 tag size is determined as 100 bps INFO @ Thu, 03 May 2018 23:12:02: #1 tag size = 100 INFO @ Thu, 03 May 2018 23:12:02: #1 total tags in treatment: 1817992 INFO @ Thu, 03 May 2018 23:12:02: #1 user defined the maximum tags... INFO @ Thu, 03 May 2018 23:12:02: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 03 May 2018 23:12:02: #1 tags after filtering in treatment: 1606246 INFO @ Thu, 03 May 2018 23:12:02: #1 Redundant rate of treatment: 0.12 INFO @ Thu, 03 May 2018 23:12:02: #1 finished! INFO @ Thu, 03 May 2018 23:12:02: #2 Build Peak Model... INFO @ Thu, 03 May 2018 23:12:02: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 03 May 2018 23:12:02: #2 number of paired peaks: 57 WARNING @ Thu, 03 May 2018 23:12:02: Too few paired peaks (57) 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 @ Thu, 03 May 2018 23:12:02: Process for pairing-model is terminated! cat: SRX3063103.05_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 `SRX3063103.05_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 `SRX3063103.05_*.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 `SRX3063103.05_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 @ Thu, 03 May 2018 23:12:06: #1 tag size is determined as 100 bps INFO @ Thu, 03 May 2018 23:12:06: #1 tag size = 100 INFO @ Thu, 03 May 2018 23:12:06: #1 total tags in treatment: 1817992 INFO @ Thu, 03 May 2018 23:12:06: #1 user defined the maximum tags... INFO @ Thu, 03 May 2018 23:12:06: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 03 May 2018 23:12:06: #1 tag size is determined as 100 bps INFO @ Thu, 03 May 2018 23:12:06: #1 tag size = 100 INFO @ Thu, 03 May 2018 23:12:06: #1 total tags in treatment: 1817992 INFO @ Thu, 03 May 2018 23:12:06: #1 user defined the maximum tags... INFO @ Thu, 03 May 2018 23:12:06: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 03 May 2018 23:12:06: #1 tags after filtering in treatment: 1606246 INFO @ Thu, 03 May 2018 23:12:06: #1 Redundant rate of treatment: 0.12 INFO @ Thu, 03 May 2018 23:12:06: #1 finished! INFO @ Thu, 03 May 2018 23:12:06: #2 Build Peak Model... INFO @ Thu, 03 May 2018 23:12:06: #1 tags after filtering in treatment: 1606246 INFO @ Thu, 03 May 2018 23:12:06: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 03 May 2018 23:12:06: #1 Redundant rate of treatment: 0.12 INFO @ Thu, 03 May 2018 23:12:06: #1 finished! INFO @ Thu, 03 May 2018 23:12:06: #2 Build Peak Model... INFO @ Thu, 03 May 2018 23:12:06: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 03 May 2018 23:12:06: #2 number of paired peaks: 57 WARNING @ Thu, 03 May 2018 23:12:06: Too few paired peaks (57) 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 @ Thu, 03 May 2018 23:12:06: Process for pairing-model is terminated! cat: SRX3063103.10_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 @ Thu, 03 May 2018 23:12:06: #2 number of paired peaks: 57 WARNING @ Thu, 03 May 2018 23:12:06: Too few paired peaks (57) 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 @ Thu, 03 May 2018 23:12:06: Process for pairing-model is terminated! pass1 - making usageList (0 chroms): 0 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX3063103.10_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 `SRX3063103.10_*.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 `SRX3063103.10_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 cat: SRX3063103.20_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 `SRX3063103.20_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 `SRX3063103.20_*.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 `SRX3063103.20_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。