Job ID = 11296254 sra ファイルのダウンロード中... Completed: 549003K bytes transferred in 16 seconds (278134K 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: SINGLE fastq に変換中... Read 19842080 spots for /home/okishinya/chipatlas/results/sacCer3/SRX2969192/SRR5770179.sra Written 19842080 spots for /home/okishinya/chipatlas/results/sacCer3/SRX2969192/SRR5770179.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: 00:03:26 19842080 reads; of these: 19842080 (100.00%) were unpaired; of these: 561565 (2.83%) aligned 0 times 16754527 (84.44%) aligned exactly 1 time 2525988 (12.73%) aligned >1 times 97.17% overall alignment rate Time searching: 00:03:26 Overall time: 00:03:26 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_sort_core] merging from 8 files... [bam_rmdupse_core] 7791815 / 19280515 = 0.4041 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 @ Mon, 05 Nov 2018 17:57:17: # Command line: callpeak -t SRX2969192.bam -f BAM -g 12100000 -n SRX2969192.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX2969192.10 # format = BAM # ChIP-seq file = ['SRX2969192.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 @ Mon, 05 Nov 2018 17:57:17: #1 read tag files... INFO @ Mon, 05 Nov 2018 17:57:17: #1 read treatment tags... INFO @ Mon, 05 Nov 2018 17:57:17: # Command line: callpeak -t SRX2969192.bam -f BAM -g 12100000 -n SRX2969192.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX2969192.05 # format = BAM # ChIP-seq file = ['SRX2969192.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 @ Mon, 05 Nov 2018 17:57:17: #1 read tag files... INFO @ Mon, 05 Nov 2018 17:57:17: #1 read treatment tags... INFO @ Mon, 05 Nov 2018 17:57:17: # Command line: callpeak -t SRX2969192.bam -f BAM -g 12100000 -n SRX2969192.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX2969192.20 # format = BAM # ChIP-seq file = ['SRX2969192.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 @ Mon, 05 Nov 2018 17:57:17: #1 read tag files... INFO @ Mon, 05 Nov 2018 17:57:17: #1 read treatment tags... INFO @ Mon, 05 Nov 2018 17:57:23: 1000000 INFO @ Mon, 05 Nov 2018 17:57:23: 1000000 INFO @ Mon, 05 Nov 2018 17:57:23: 1000000 INFO @ Mon, 05 Nov 2018 17:57:29: 2000000 INFO @ Mon, 05 Nov 2018 17:57:29: 2000000 INFO @ Mon, 05 Nov 2018 17:57:29: 2000000 INFO @ Mon, 05 Nov 2018 17:57:35: 3000000 INFO @ Mon, 05 Nov 2018 17:57:35: 3000000 INFO @ Mon, 05 Nov 2018 17:57:36: 3000000 INFO @ Mon, 05 Nov 2018 17:57:41: 4000000 INFO @ Mon, 05 Nov 2018 17:57:41: 4000000 INFO @ Mon, 05 Nov 2018 17:57:42: 4000000 INFO @ Mon, 05 Nov 2018 17:57:47: 5000000 INFO @ Mon, 05 Nov 2018 17:57:48: 5000000 INFO @ Mon, 05 Nov 2018 17:57:48: 5000000 INFO @ Mon, 05 Nov 2018 17:57:53: 6000000 INFO @ Mon, 05 Nov 2018 17:57:54: 6000000 INFO @ Mon, 05 Nov 2018 17:57:54: 6000000 INFO @ Mon, 05 Nov 2018 17:58:00: 7000000 INFO @ Mon, 05 Nov 2018 17:58:00: 7000000 INFO @ Mon, 05 Nov 2018 17:58:01: 7000000 INFO @ Mon, 05 Nov 2018 17:58:06: 8000000 INFO @ Mon, 05 Nov 2018 17:58:07: 8000000 INFO @ Mon, 05 Nov 2018 17:58:07: 8000000 INFO @ Mon, 05 Nov 2018 17:58:12: 9000000 INFO @ Mon, 05 Nov 2018 17:58:13: 9000000 INFO @ Mon, 05 Nov 2018 17:58:14: 9000000 INFO @ Mon, 05 Nov 2018 17:58:18: 10000000 INFO @ Mon, 05 Nov 2018 17:58:19: 10000000 INFO @ Mon, 05 Nov 2018 17:58:20: 10000000 INFO @ Mon, 05 Nov 2018 17:58:25: 11000000 INFO @ Mon, 05 Nov 2018 17:58:26: 11000000 INFO @ Mon, 05 Nov 2018 17:58:26: 11000000 INFO @ Mon, 05 Nov 2018 17:58:28: #1 tag size is determined as 50 bps INFO @ Mon, 05 Nov 2018 17:58:28: #1 tag size = 50 INFO @ Mon, 05 Nov 2018 17:58:28: #1 total tags in treatment: 11488700 INFO @ Mon, 05 Nov 2018 17:58:28: #1 user defined the maximum tags... INFO @ Mon, 05 Nov 2018 17:58:28: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 05 Nov 2018 17:58:28: #1 tags after filtering in treatment: 11488700 INFO @ Mon, 05 Nov 2018 17:58:28: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 05 Nov 2018 17:58:28: #1 finished! INFO @ Mon, 05 Nov 2018 17:58:28: #2 Build Peak Model... INFO @ Mon, 05 Nov 2018 17:58:28: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 05 Nov 2018 17:58:28: #2 number of paired peaks: 0 WARNING @ Mon, 05 Nov 2018 17:58:28: Too few paired peaks (0) 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 @ Mon, 05 Nov 2018 17:58:28: Process for pairing-model is terminated! cat: SRX2969192.10_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): 0 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX2969192.10_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 `SRX2969192.10_*.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 `SRX2969192.10_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 @ Mon, 05 Nov 2018 17:58:29: #1 tag size is determined as 50 bps INFO @ Mon, 05 Nov 2018 17:58:29: #1 tag size = 50 INFO @ Mon, 05 Nov 2018 17:58:29: #1 total tags in treatment: 11488700 INFO @ Mon, 05 Nov 2018 17:58:29: #1 user defined the maximum tags... INFO @ Mon, 05 Nov 2018 17:58:29: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 05 Nov 2018 17:58:29: #1 tags after filtering in treatment: 11488700 INFO @ Mon, 05 Nov 2018 17:58:29: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 05 Nov 2018 17:58:29: #1 finished! INFO @ Mon, 05 Nov 2018 17:58:29: #2 Build Peak Model... INFO @ Mon, 05 Nov 2018 17:58:29: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 05 Nov 2018 17:58:29: #1 tag size is determined as 50 bps INFO @ Mon, 05 Nov 2018 17:58:29: #1 tag size = 50 INFO @ Mon, 05 Nov 2018 17:58:29: #1 total tags in treatment: 11488700 INFO @ Mon, 05 Nov 2018 17:58:29: #1 user defined the maximum tags... INFO @ Mon, 05 Nov 2018 17:58:29: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 05 Nov 2018 17:58:30: #1 tags after filtering in treatment: 11488700 INFO @ Mon, 05 Nov 2018 17:58:30: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 05 Nov 2018 17:58:30: #1 finished! INFO @ Mon, 05 Nov 2018 17:58:30: #2 Build Peak Model... INFO @ Mon, 05 Nov 2018 17:58:30: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 05 Nov 2018 17:58:30: #2 number of paired peaks: 0 WARNING @ Mon, 05 Nov 2018 17:58:30: Too few paired peaks (0) 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 @ Mon, 05 Nov 2018 17:58:30: Process for pairing-model is terminated! cat: SRX2969192.05_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 `SRX2969192.05_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 `SRX2969192.05_*.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 `SRX2969192.05_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 @ Mon, 05 Nov 2018 17:58:30: #2 number of paired peaks: 0 WARNING @ Mon, 05 Nov 2018 17:58:30: Too few paired peaks (0) 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 @ Mon, 05 Nov 2018 17:58:30: Process for pairing-model is terminated! cat: SRX2969192.20_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 `SRX2969192.20_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 `SRX2969192.20_*.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 `SRX2969192.20_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。