Job ID = 11633358 sra ファイルのダウンロード中... Completed: 248180K bytes transferred in 6 seconds (328873K 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 4000000 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1236137/ERR1162730.sra Written 4000000 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1236137/ERR1162730.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: 00:02:53 4000000 reads; of these: 4000000 (100.00%) were paired; of these: 454431 (11.36%) aligned concordantly 0 times 3061053 (76.53%) aligned concordantly exactly 1 time 484516 (12.11%) aligned concordantly >1 times ---- 454431 pairs aligned concordantly 0 times; of these: 36711 (8.08%) aligned discordantly 1 time ---- 417720 pairs aligned 0 times concordantly or discordantly; of these: 835440 mates make up the pairs; of these: 794683 (95.12%) aligned 0 times 22233 (2.66%) aligned exactly 1 time 18524 (2.22%) aligned >1 times 90.07% overall alignment rate Time searching: 00:02:53 Overall time: 00:02:53 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] 35839 / 3573817 = 0.0100 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, 15 Feb 2019 08:51:10: # Command line: callpeak -t ERX1236137.bam -f BAM -g 12100000 -n ERX1236137.20 -q 1e-20 # ARGUMENTS LIST: # name = ERX1236137.20 # format = BAM # ChIP-seq file = ['ERX1236137.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, 15 Feb 2019 08:51:10: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:51:10: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:51:10: # Command line: callpeak -t ERX1236137.bam -f BAM -g 12100000 -n ERX1236137.10 -q 1e-10 # ARGUMENTS LIST: # name = ERX1236137.10 # format = BAM # ChIP-seq file = ['ERX1236137.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, 15 Feb 2019 08:51:10: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:51:10: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:51:10: # Command line: callpeak -t ERX1236137.bam -f BAM -g 12100000 -n ERX1236137.05 -q 1e-05 # ARGUMENTS LIST: # name = ERX1236137.05 # format = BAM # ChIP-seq file = ['ERX1236137.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, 15 Feb 2019 08:51:10: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:51:10: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:51:15: 1000000 INFO @ Fri, 15 Feb 2019 08:51:15: 1000000 INFO @ Fri, 15 Feb 2019 08:51:15: 1000000 INFO @ Fri, 15 Feb 2019 08:51:20: 2000000 INFO @ Fri, 15 Feb 2019 08:51:21: 2000000 INFO @ Fri, 15 Feb 2019 08:51:21: 2000000 INFO @ Fri, 15 Feb 2019 08:51:26: 3000000 INFO @ Fri, 15 Feb 2019 08:51:26: 3000000 INFO @ Fri, 15 Feb 2019 08:51:26: 3000000 INFO @ Fri, 15 Feb 2019 08:51:31: 4000000 INFO @ Fri, 15 Feb 2019 08:51:31: 4000000 INFO @ Fri, 15 Feb 2019 08:51:31: 4000000 INFO @ Fri, 15 Feb 2019 08:51:36: 5000000 INFO @ Fri, 15 Feb 2019 08:51:36: 5000000 INFO @ Fri, 15 Feb 2019 08:51:37: 5000000 INFO @ Fri, 15 Feb 2019 08:51:41: 6000000 INFO @ Fri, 15 Feb 2019 08:51:42: 6000000 INFO @ Fri, 15 Feb 2019 08:51:42: 6000000 INFO @ Fri, 15 Feb 2019 08:51:47: 7000000 INFO @ Fri, 15 Feb 2019 08:51:47: 7000000 INFO @ Fri, 15 Feb 2019 08:51:47: 7000000 INFO @ Fri, 15 Feb 2019 08:51:47: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:51:47: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:51:47: #1 total tags in treatment: 3509909 INFO @ Fri, 15 Feb 2019 08:51:47: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:51:47: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 08:51:47: #1 tags after filtering in treatment: 3035117 INFO @ Fri, 15 Feb 2019 08:51:47: #1 Redundant rate of treatment: 0.14 INFO @ Fri, 15 Feb 2019 08:51:47: #1 finished! INFO @ Fri, 15 Feb 2019 08:51:47: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:51:47: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:51:48: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:51:48: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:51:48: #1 total tags in treatment: 3509909 INFO @ Fri, 15 Feb 2019 08:51:48: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:51:48: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 08:51:48: #2 number of paired peaks: 44 WARNING @ Fri, 15 Feb 2019 08:51:48: Too few paired peaks (44) 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, 15 Feb 2019 08:51:48: Process for pairing-model is terminated! cat: ERX1236137.10_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): 4 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `ERX1236137.10_model.r': そのようなファイルやディレクトリはありません INFO @ Fri, 15 Feb 2019 08:51:48: #1 tags after filtering in treatment: 3035117 INFO @ Fri, 15 Feb 2019 08:51:48: #1 Redundant rate of treatment: 0.14 INFO @ Fri, 15 Feb 2019 08:51:48: #1 finished! INFO @ Fri, 15 Feb 2019 08:51:48: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:51:48: #2 looking for paired plus/minus strand peaks... rm: cannot remove `ERX1236137.10_*.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 `ERX1236137.10_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 @ Fri, 15 Feb 2019 08:51:48: #2 number of paired peaks: 44 WARNING @ Fri, 15 Feb 2019 08:51:48: Too few paired peaks (44) 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, 15 Feb 2019 08:51:48: Process for pairing-model is terminated! cat: ERX1236137.05_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): 3 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `ERX1236137.05_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 `ERX1236137.05_*.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 `ERX1236137.05_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 @ Fri, 15 Feb 2019 08:51:48: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:51:48: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:51:48: #1 total tags in treatment: 3509909 INFO @ Fri, 15 Feb 2019 08:51:48: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:51:48: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 08:51:48: #1 tags after filtering in treatment: 3035117 INFO @ Fri, 15 Feb 2019 08:51:48: #1 Redundant rate of treatment: 0.14 INFO @ Fri, 15 Feb 2019 08:51:48: #1 finished! INFO @ Fri, 15 Feb 2019 08:51:48: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:51:48: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:51:48: #2 number of paired peaks: 44 WARNING @ Fri, 15 Feb 2019 08:51:48: Too few paired peaks (44) 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, 15 Feb 2019 08:51:48: Process for pairing-model is terminated! cat: ERX1236137.20_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): 3 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `ERX1236137.20_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 `ERX1236137.20_*.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 `ERX1236137.20_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。