Job ID = 11193198 sra ファイルのダウンロード中... Completed: 279201K bytes transferred in 7 seconds (319949K 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 6380225 spots for /home/okishinya/chipatlas/results/sacCer3/SRX876287/SRR1802390.sra Written 6380225 spots for /home/okishinya/chipatlas/results/sacCer3/SRX876287/SRR1802390.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: 00:02:13 6380225 reads; of these: 6380225 (100.00%) were paired; of these: 3880520 (60.82%) aligned concordantly 0 times 2094964 (32.84%) aligned concordantly exactly 1 time 404741 (6.34%) aligned concordantly >1 times ---- 3880520 pairs aligned concordantly 0 times; of these: 62744 (1.62%) aligned discordantly 1 time ---- 3817776 pairs aligned 0 times concordantly or discordantly; of these: 7635552 mates make up the pairs; of these: 7495509 (98.17%) aligned 0 times 88271 (1.16%) aligned exactly 1 time 51772 (0.68%) aligned >1 times 41.26% overall alignment rate Time searching: 00:02:13 Overall time: 00:02:13 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] 1512606 / 2545287 = 0.5943 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 11:10:43: # Command line: callpeak -t SRX876287.bam -f BAM -g 12100000 -n SRX876287.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX876287.10 # format = BAM # ChIP-seq file = ['SRX876287.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 11:10:43: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:10:43: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:10:43: # Command line: callpeak -t SRX876287.bam -f BAM -g 12100000 -n SRX876287.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX876287.20 # format = BAM # ChIP-seq file = ['SRX876287.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 11:10:43: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:10:43: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:10:43: # Command line: callpeak -t SRX876287.bam -f BAM -g 12100000 -n SRX876287.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX876287.05 # format = BAM # ChIP-seq file = ['SRX876287.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 11:10:43: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:10:43: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:10:50: 1000000 INFO @ Sat, 15 Sep 2018 11:10:50: 1000000 INFO @ Sat, 15 Sep 2018 11:10:50: 1000000 INFO @ Sat, 15 Sep 2018 11:10:56: 2000000 INFO @ Sat, 15 Sep 2018 11:10:56: 2000000 INFO @ Sat, 15 Sep 2018 11:10:56: 2000000 INFO @ Sat, 15 Sep 2018 11:10:58: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 11:10:58: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 11:10:58: #1 total tags in treatment: 1020577 INFO @ Sat, 15 Sep 2018 11:10:58: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:10:58: #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 11:10:58: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 11:10:58: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 11:10:58: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 11:10:58: #1 total tags in treatment: 1020577 INFO @ Sat, 15 Sep 2018 11:10:58: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 11:10:58: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:10:58: #1 total tags in treatment: 1020577 INFO @ Sat, 15 Sep 2018 11:10:58: #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 11:10:58: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:10:58: #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 11:10:58: #1 tags after filtering in treatment: 868529 INFO @ Sat, 15 Sep 2018 11:10:58: #1 Redundant rate of treatment: 0.15 INFO @ Sat, 15 Sep 2018 11:10:58: #1 finished! INFO @ Sat, 15 Sep 2018 11:10:58: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:10:58: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:10:58: #1 tags after filtering in treatment: 868529 INFO @ Sat, 15 Sep 2018 11:10:58: #1 Redundant rate of treatment: 0.15 INFO @ Sat, 15 Sep 2018 11:10:58: #1 finished! INFO @ Sat, 15 Sep 2018 11:10:58: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:10:58: #1 tags after filtering in treatment: 868529 INFO @ Sat, 15 Sep 2018 11:10:58: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:10:58: #1 Redundant rate of treatment: 0.15 INFO @ Sat, 15 Sep 2018 11:10:58: #1 finished! INFO @ Sat, 15 Sep 2018 11:10:58: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:10:58: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:10:58: #2 number of paired peaks: 59 WARNING @ Sat, 15 Sep 2018 11:10:58: Too few paired peaks (59) 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 11:10:58: Process for pairing-model is terminated! INFO @ Sat, 15 Sep 2018 11:10:58: #2 number of paired peaks: 59 WARNING @ Sat, 15 Sep 2018 11:10:58: Too few paired peaks (59) 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 11:10:58: Process for pairing-model is terminated! INFO @ Sat, 15 Sep 2018 11:10:58: #2 number of paired peaks: 59 WARNING @ Sat, 15 Sep 2018 11:10:58: Too few paired peaks (59) 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 11:10:58: Process for pairing-model is terminated! cat: SRX876287.05_peaks.narrowPeak: そのようなファイルやディレクトリはありません cat: SRX876287.20_peaks.narrowPeak: そのようなファイルやディレクトリはありません cat: SRX876287.10_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 `SRX876287.05_model.r': そのようなファイルやディレクトリはありません pass1 - making usageList (0 chroms): 1 millis rm: cannot remove `SRX876287.05_*.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 `SRX876287.05_peaks.narrowPeak': そのようなファイルやディレクトリはありません needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX876287.20_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 `SRX876287.20_*.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 `SRX876287.20_peaks.narrowPeak': そのようなファイルやディレクトリはありません rm: cannot remove `SRX876287.10_model.r': そのようなファイルやディレクトリはありません CompletedMACS2peakCalling rm: cannot remove `SRX876287.10_*.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 `SRX876287.10_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。