Job ID = 11192931 sra ファイルのダウンロード中... Completed: 445247K bytes transferred in 6 seconds (534025K 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 12062354 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3242047/SRR6129615.sra Written 12062354 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3242047/SRR6129615.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: 00:03:10 12062354 reads; of these: 12062354 (100.00%) were paired; of these: 11507321 (95.40%) aligned concordantly 0 times 418414 (3.47%) aligned concordantly exactly 1 time 136619 (1.13%) aligned concordantly >1 times ---- 11507321 pairs aligned concordantly 0 times; of these: 271002 (2.36%) aligned discordantly 1 time ---- 11236319 pairs aligned 0 times concordantly or discordantly; of these: 22472638 mates make up the pairs; of these: 20113722 (89.50%) aligned 0 times 1884422 (8.39%) aligned exactly 1 time 474494 (2.11%) aligned >1 times 16.63% overall alignment rate Time searching: 00:03:10 Overall time: 00:03:10 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] 360563 / 820527 = 0.4394 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 @ Sat, 15 Sep 2018 10:37:39: # Command line: callpeak -t SRX3242047.bam -f BAM -g 12100000 -n SRX3242047.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3242047.05 # format = BAM # ChIP-seq file = ['SRX3242047.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 @ Sat, 15 Sep 2018 10:37:39: #1 read tag files... INFO @ Sat, 15 Sep 2018 10:37:39: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 10:37:39: # Command line: callpeak -t SRX3242047.bam -f BAM -g 12100000 -n SRX3242047.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3242047.10 # format = BAM # ChIP-seq file = ['SRX3242047.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 @ Sat, 15 Sep 2018 10:37:39: #1 read tag files... INFO @ Sat, 15 Sep 2018 10:37:39: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 10:37:39: # Command line: callpeak -t SRX3242047.bam -f BAM -g 12100000 -n SRX3242047.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3242047.20 # format = BAM # ChIP-seq file = ['SRX3242047.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 @ Sat, 15 Sep 2018 10:37:39: #1 read tag files... INFO @ Sat, 15 Sep 2018 10:37:39: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 10:37:44: 1000000 INFO @ Sat, 15 Sep 2018 10:37:44: 1000000 INFO @ Sat, 15 Sep 2018 10:37:44: 1000000 INFO @ Sat, 15 Sep 2018 10:37:49: 2000000 INFO @ Sat, 15 Sep 2018 10:37:49: 2000000 INFO @ Sat, 15 Sep 2018 10:37:49: 2000000 INFO @ Sat, 15 Sep 2018 10:37:54: 3000000 INFO @ Sat, 15 Sep 2018 10:37:54: 3000000 INFO @ Sat, 15 Sep 2018 10:37:54: 3000000 INFO @ Sat, 15 Sep 2018 10:37:56: #1 tag size is determined as 37 bps INFO @ Sat, 15 Sep 2018 10:37:56: #1 tag size = 37 INFO @ Sat, 15 Sep 2018 10:37:56: #1 total tags in treatment: 371662 INFO @ Sat, 15 Sep 2018 10:37:56: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 10:37:56: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 10:37:56: #1 tags after filtering in treatment: 298667 INFO @ Sat, 15 Sep 2018 10:37:56: #1 Redundant rate of treatment: 0.20 INFO @ Sat, 15 Sep 2018 10:37:56: #1 finished! INFO @ Sat, 15 Sep 2018 10:37:56: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 10:37:56: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 10:37:56: #1 tag size is determined as 37 bps INFO @ Sat, 15 Sep 2018 10:37:56: #1 tag size = 37 INFO @ Sat, 15 Sep 2018 10:37:56: #1 total tags in treatment: 371662 INFO @ Sat, 15 Sep 2018 10:37:56: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 10:37:56: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 10:37:56: #1 tags after filtering in treatment: 298667 INFO @ Sat, 15 Sep 2018 10:37:56: #1 Redundant rate of treatment: 0.20 INFO @ Sat, 15 Sep 2018 10:37:56: #1 finished! INFO @ Sat, 15 Sep 2018 10:37:56: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 10:37:56: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 10:37:56: #2 number of paired peaks: 73 WARNING @ Sat, 15 Sep 2018 10:37:56: Too few paired peaks (73) 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 @ Sat, 15 Sep 2018 10:37:56: Process for pairing-model is terminated! cat: SRX3242047.20_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): 0 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX3242047.20_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 `SRX3242047.20_*.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 `SRX3242047.20_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 @ Sat, 15 Sep 2018 10:37:56: #2 number of paired peaks: 73 WARNING @ Sat, 15 Sep 2018 10:37:56: Too few paired peaks (73) 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 @ Sat, 15 Sep 2018 10:37:56: Process for pairing-model is terminated! cat: SRX3242047.05_peaks.narrowPeak: そのようなファイルやディレクトリはありません INFO @ Sat, 15 Sep 2018 10:37:56: #1 tag size is determined as 37 bps INFO @ Sat, 15 Sep 2018 10:37:56: #1 tag size = 37 INFO @ Sat, 15 Sep 2018 10:37:56: #1 total tags in treatment: 371662 INFO @ Sat, 15 Sep 2018 10:37:56: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 10:37:56: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX3242047.05_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 `SRX3242047.05_*.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 `SRX3242047.05_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 @ Sat, 15 Sep 2018 10:37:56: #1 tags after filtering in treatment: 298667 INFO @ Sat, 15 Sep 2018 10:37:56: #1 Redundant rate of treatment: 0.20 INFO @ Sat, 15 Sep 2018 10:37:56: #1 finished! INFO @ Sat, 15 Sep 2018 10:37:56: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 10:37:56: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 10:37:56: #2 number of paired peaks: 73 WARNING @ Sat, 15 Sep 2018 10:37:56: Too few paired peaks (73) 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 @ Sat, 15 Sep 2018 10:37:56: Process for pairing-model is terminated! cat: SRX3242047.10_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 `SRX3242047.10_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 `SRX3242047.10_*.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 `SRX3242047.10_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 BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。