Job ID = 11296952 sra ファイルのダウンロード中... Completed: 226837K bytes transferred in 6 seconds (292885K 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 10857111 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3856374/SRR6908192.sra Written 10857111 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3856374/SRR6908192.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: 00:01:50 10857111 reads; of these: 10857111 (100.00%) were unpaired; of these: 619343 (5.70%) aligned 0 times 7479988 (68.89%) aligned exactly 1 time 2757780 (25.40%) aligned >1 times 94.30% overall alignment rate Time searching: 00:01:50 Overall time: 00:01:50 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] 4931443 / 10237768 = 0.4817 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 18:04:44: # Command line: callpeak -t SRX3856374.bam -f BAM -g 12100000 -n SRX3856374.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3856374.20 # format = BAM # ChIP-seq file = ['SRX3856374.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 18:04:44: #1 read tag files... INFO @ Mon, 05 Nov 2018 18:04:44: #1 read treatment tags... INFO @ Mon, 05 Nov 2018 18:04:44: # Command line: callpeak -t SRX3856374.bam -f BAM -g 12100000 -n SRX3856374.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3856374.05 # format = BAM # ChIP-seq file = ['SRX3856374.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 18:04:44: #1 read tag files... INFO @ Mon, 05 Nov 2018 18:04:44: #1 read treatment tags... INFO @ Mon, 05 Nov 2018 18:04:44: # Command line: callpeak -t SRX3856374.bam -f BAM -g 12100000 -n SRX3856374.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3856374.10 # format = BAM # ChIP-seq file = ['SRX3856374.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 18:04:44: #1 read tag files... INFO @ Mon, 05 Nov 2018 18:04:44: #1 read treatment tags... INFO @ Mon, 05 Nov 2018 18:04:50: 1000000 INFO @ Mon, 05 Nov 2018 18:04:50: 1000000 INFO @ Mon, 05 Nov 2018 18:04:50: 1000000 INFO @ Mon, 05 Nov 2018 18:04:56: 2000000 INFO @ Mon, 05 Nov 2018 18:04:56: 2000000 INFO @ Mon, 05 Nov 2018 18:04:56: 2000000 INFO @ Mon, 05 Nov 2018 18:05:02: 3000000 INFO @ Mon, 05 Nov 2018 18:05:02: 3000000 INFO @ Mon, 05 Nov 2018 18:05:02: 3000000 INFO @ Mon, 05 Nov 2018 18:05:08: 4000000 INFO @ Mon, 05 Nov 2018 18:05:08: 4000000 INFO @ Mon, 05 Nov 2018 18:05:09: 4000000 INFO @ Mon, 05 Nov 2018 18:05:14: 5000000 INFO @ Mon, 05 Nov 2018 18:05:14: 5000000 INFO @ Mon, 05 Nov 2018 18:05:15: 5000000 INFO @ Mon, 05 Nov 2018 18:05:16: #1 tag size is determined as 50 bps INFO @ Mon, 05 Nov 2018 18:05:16: #1 tag size = 50 INFO @ Mon, 05 Nov 2018 18:05:16: #1 total tags in treatment: 5306325 INFO @ Mon, 05 Nov 2018 18:05:16: #1 user defined the maximum tags... INFO @ Mon, 05 Nov 2018 18:05:16: #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 18:05:16: #1 tags after filtering in treatment: 5306325 INFO @ Mon, 05 Nov 2018 18:05:16: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 05 Nov 2018 18:05:16: #1 finished! INFO @ Mon, 05 Nov 2018 18:05:16: #2 Build Peak Model... INFO @ Mon, 05 Nov 2018 18:05:16: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 05 Nov 2018 18:05:16: #1 tag size is determined as 50 bps INFO @ Mon, 05 Nov 2018 18:05:16: #1 tag size = 50 INFO @ Mon, 05 Nov 2018 18:05:16: #1 total tags in treatment: 5306325 INFO @ Mon, 05 Nov 2018 18:05:16: #1 user defined the maximum tags... INFO @ Mon, 05 Nov 2018 18:05:16: #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 18:05:16: #2 number of paired peaks: 0 WARNING @ Mon, 05 Nov 2018 18:05:16: 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 18:05:16: Process for pairing-model is terminated! cat: SRX3856374.20_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 `SRX3856374.20_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 `SRX3856374.20_*.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 `SRX3856374.20_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 INFO @ Mon, 05 Nov 2018 18:05:16: #1 tags after filtering in treatment: 5306325 INFO @ Mon, 05 Nov 2018 18:05:16: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 05 Nov 2018 18:05:16: #1 finished! INFO @ Mon, 05 Nov 2018 18:05:16: #2 Build Peak Model... INFO @ Mon, 05 Nov 2018 18:05:16: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 05 Nov 2018 18:05:17: #2 number of paired peaks: 0 WARNING @ Mon, 05 Nov 2018 18:05:17: 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 18:05:17: Process for pairing-model is terminated! cat: SRX3856374.10_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): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX3856374.10_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 `SRX3856374.10_*.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 `SRX3856374.10_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 18:05:17: #1 tag size is determined as 50 bps INFO @ Mon, 05 Nov 2018 18:05:17: #1 tag size = 50 INFO @ Mon, 05 Nov 2018 18:05:17: #1 total tags in treatment: 5306325 INFO @ Mon, 05 Nov 2018 18:05:17: #1 user defined the maximum tags... INFO @ Mon, 05 Nov 2018 18:05:17: #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 18:05:17: #1 tags after filtering in treatment: 5306325 INFO @ Mon, 05 Nov 2018 18:05:17: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 05 Nov 2018 18:05:17: #1 finished! INFO @ Mon, 05 Nov 2018 18:05:17: #2 Build Peak Model... INFO @ Mon, 05 Nov 2018 18:05:17: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 05 Nov 2018 18:05:17: #2 number of paired peaks: 0 WARNING @ Mon, 05 Nov 2018 18:05:17: 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 18:05:17: Process for pairing-model is terminated! cat: SRX3856374.05_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 `SRX3856374.05_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 `SRX3856374.05_*.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 `SRX3856374.05_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 BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。