Job ID = 11633117 sra ファイルのダウンロード中... Completed: 242185K bytes transferred in 7 seconds (283263K 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/ERX1174053/ERR1094567.sra Written 4000000 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1174053/ERR1094567.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: 00:03:02 4000000 reads; of these: 4000000 (100.00%) were paired; of these: 180106 (4.50%) aligned concordantly 0 times 3584259 (89.61%) aligned concordantly exactly 1 time 235635 (5.89%) aligned concordantly >1 times ---- 180106 pairs aligned concordantly 0 times; of these: 103997 (57.74%) aligned discordantly 1 time ---- 76109 pairs aligned 0 times concordantly or discordantly; of these: 152218 mates make up the pairs; of these: 122457 (80.45%) aligned 0 times 14209 (9.33%) aligned exactly 1 time 15552 (10.22%) aligned >1 times 98.47% overall alignment rate Time searching: 00:03:02 Overall time: 00:03:02 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] 18247 / 3917510 = 0.0047 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 08:22:49: # Command line: callpeak -t ERX1174053.bam -f BAM -g 12100000 -n ERX1174053.05 -q 1e-05 # ARGUMENTS LIST: # name = ERX1174053.05 # format = BAM # ChIP-seq file = ['ERX1174053.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 08:22:49: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:22:49: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:22:49: # Command line: callpeak -t ERX1174053.bam -f BAM -g 12100000 -n ERX1174053.20 -q 1e-20 # ARGUMENTS LIST: # name = ERX1174053.20 # format = BAM # ChIP-seq file = ['ERX1174053.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 08:22:49: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:22:49: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:22:49: # Command line: callpeak -t ERX1174053.bam -f BAM -g 12100000 -n ERX1174053.10 -q 1e-10 # ARGUMENTS LIST: # name = ERX1174053.10 # format = BAM # ChIP-seq file = ['ERX1174053.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 08:22:49: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:22:49: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:22:55: 1000000 INFO @ Fri, 15 Feb 2019 08:22:55: 1000000 INFO @ Fri, 15 Feb 2019 08:22:55: 1000000 INFO @ Fri, 15 Feb 2019 08:23:00: 2000000 INFO @ Fri, 15 Feb 2019 08:23:00: 2000000 INFO @ Fri, 15 Feb 2019 08:23:01: 2000000 INFO @ Fri, 15 Feb 2019 08:23:06: 3000000 INFO @ Fri, 15 Feb 2019 08:23:06: 3000000 INFO @ Fri, 15 Feb 2019 08:23:06: 3000000 INFO @ Fri, 15 Feb 2019 08:23:11: 4000000 INFO @ Fri, 15 Feb 2019 08:23:12: 4000000 INFO @ Fri, 15 Feb 2019 08:23:12: 4000000 INFO @ Fri, 15 Feb 2019 08:23:17: 5000000 INFO @ Fri, 15 Feb 2019 08:23:18: 5000000 INFO @ Fri, 15 Feb 2019 08:23:18: 5000000 INFO @ Fri, 15 Feb 2019 08:23:22: 6000000 INFO @ Fri, 15 Feb 2019 08:23:24: 6000000 INFO @ Fri, 15 Feb 2019 08:23:24: 6000000 INFO @ Fri, 15 Feb 2019 08:23:28: 7000000 INFO @ Fri, 15 Feb 2019 08:23:29: 7000000 INFO @ Fri, 15 Feb 2019 08:23:30: 7000000 INFO @ Fri, 15 Feb 2019 08:23:32: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:23:32: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:23:32: #1 total tags in treatment: 3802031 INFO @ Fri, 15 Feb 2019 08:23:32: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:23:32: #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 08:23:32: #1 tags after filtering in treatment: 3446755 INFO @ Fri, 15 Feb 2019 08:23:32: #1 Redundant rate of treatment: 0.09 INFO @ Fri, 15 Feb 2019 08:23:32: #1 finished! INFO @ Fri, 15 Feb 2019 08:23:32: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:23:32: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:23:33: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 08:23:33: 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 @ Fri, 15 Feb 2019 08:23:33: Process for pairing-model is terminated! cat: ERX1174053.20_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): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `ERX1174053.20_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 `ERX1174053.20_*.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 `ERX1174053.20_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 @ Fri, 15 Feb 2019 08:23:34: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:23:34: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:23:34: #1 total tags in treatment: 3802031 INFO @ Fri, 15 Feb 2019 08:23:34: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:23:34: #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 08:23:34: #1 tags after filtering in treatment: 3446755 INFO @ Fri, 15 Feb 2019 08:23:34: #1 Redundant rate of treatment: 0.09 INFO @ Fri, 15 Feb 2019 08:23:34: #1 finished! INFO @ Fri, 15 Feb 2019 08:23:34: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:23:34: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:23:34: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 08:23:34: 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 @ Fri, 15 Feb 2019 08:23:34: Process for pairing-model is terminated! cat: ERX1174053.05_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): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `ERX1174053.05_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 `ERX1174053.05_*.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 `ERX1174053.05_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 08:23:35: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:23:35: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:23:35: #1 total tags in treatment: 3802031 INFO @ Fri, 15 Feb 2019 08:23:35: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:23:35: #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 08:23:35: #1 tags after filtering in treatment: 3446755 INFO @ Fri, 15 Feb 2019 08:23:35: #1 Redundant rate of treatment: 0.09 INFO @ Fri, 15 Feb 2019 08:23:35: #1 finished! INFO @ Fri, 15 Feb 2019 08:23:35: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:23:35: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:23:35: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 08:23:35: 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 @ Fri, 15 Feb 2019 08:23:35: Process for pairing-model is terminated! cat: ERX1174053.10_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): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `ERX1174053.10_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 `ERX1174053.10_*.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 `ERX1174053.10_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。