Job ID = 11633134 sra ファイルのダウンロード中... Completed: 245023K bytes transferred in 6 seconds (322296K 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/ERX1174070/ERR1094584.sra Written 4000000 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1174070/ERR1094584.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: 00:03:03 4000000 reads; of these: 4000000 (100.00%) were paired; of these: 188492 (4.71%) aligned concordantly 0 times 3576466 (89.41%) aligned concordantly exactly 1 time 235042 (5.88%) aligned concordantly >1 times ---- 188492 pairs aligned concordantly 0 times; of these: 111283 (59.04%) aligned discordantly 1 time ---- 77209 pairs aligned 0 times concordantly or discordantly; of these: 154418 mates make up the pairs; of these: 121664 (78.79%) aligned 0 times 16330 (10.58%) aligned exactly 1 time 16424 (10.64%) aligned >1 times 98.48% overall alignment rate Time searching: 00:03:03 Overall time: 00:03:03 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] 18161 / 3916346 = 0.0046 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 08:24:34: # Command line: callpeak -t ERX1174070.bam -f BAM -g 12100000 -n ERX1174070.10 -q 1e-10 # ARGUMENTS LIST: # name = ERX1174070.10 # format = BAM # ChIP-seq file = ['ERX1174070.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 08:24:34: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:24:34: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:24:34: # Command line: callpeak -t ERX1174070.bam -f BAM -g 12100000 -n ERX1174070.05 -q 1e-05 # ARGUMENTS LIST: # name = ERX1174070.05 # format = BAM # ChIP-seq file = ['ERX1174070.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 08:24:34: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:24:34: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:24:34: # Command line: callpeak -t ERX1174070.bam -f BAM -g 12100000 -n ERX1174070.20 -q 1e-20 # ARGUMENTS LIST: # name = ERX1174070.20 # format = BAM # ChIP-seq file = ['ERX1174070.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 08:24:34: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:24:34: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:24:40: 1000000 INFO @ Fri, 15 Feb 2019 08:24:40: 1000000 INFO @ Fri, 15 Feb 2019 08:24:41: 1000000 INFO @ Fri, 15 Feb 2019 08:24:46: 2000000 INFO @ Fri, 15 Feb 2019 08:24:46: 2000000 INFO @ Fri, 15 Feb 2019 08:24:47: 2000000 INFO @ Fri, 15 Feb 2019 08:24:51: 3000000 INFO @ Fri, 15 Feb 2019 08:24:51: 3000000 INFO @ Fri, 15 Feb 2019 08:24:53: 3000000 INFO @ Fri, 15 Feb 2019 08:24:57: 4000000 INFO @ Fri, 15 Feb 2019 08:24:57: 4000000 INFO @ Fri, 15 Feb 2019 08:24:59: 4000000 INFO @ Fri, 15 Feb 2019 08:25:02: 5000000 INFO @ Fri, 15 Feb 2019 08:25:03: 5000000 INFO @ Fri, 15 Feb 2019 08:25:05: 5000000 INFO @ Fri, 15 Feb 2019 08:25:08: 6000000 INFO @ Fri, 15 Feb 2019 08:25:08: 6000000 INFO @ Fri, 15 Feb 2019 08:25:11: 6000000 INFO @ Fri, 15 Feb 2019 08:25:14: 7000000 INFO @ Fri, 15 Feb 2019 08:25:14: 7000000 INFO @ Fri, 15 Feb 2019 08:25:16: 7000000 INFO @ Fri, 15 Feb 2019 08:25:18: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:25:18: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:25:18: #1 total tags in treatment: 3793768 INFO @ Fri, 15 Feb 2019 08:25:18: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:25:18: #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 08:25:18: #1 tags after filtering in treatment: 3440385 INFO @ Fri, 15 Feb 2019 08:25:18: #1 Redundant rate of treatment: 0.09 INFO @ Fri, 15 Feb 2019 08:25:18: #1 finished! INFO @ Fri, 15 Feb 2019 08:25:18: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:25:18: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:25:19: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 08:25:19: 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 08:25:19: Process for pairing-model is terminated! cat: ERX1174070.05_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 @ Fri, 15 Feb 2019 08:25:19: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:25:19: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:25:19: #1 total tags in treatment: 3793768 INFO @ Fri, 15 Feb 2019 08:25:19: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:25:19: #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): 3 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `ERX1174070.05_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 `ERX1174070.05_*.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 `ERX1174070.05_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 08:25:19: #1 tags after filtering in treatment: 3440385 INFO @ Fri, 15 Feb 2019 08:25:19: #1 Redundant rate of treatment: 0.09 INFO @ Fri, 15 Feb 2019 08:25:19: #1 finished! INFO @ Fri, 15 Feb 2019 08:25:19: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:25:19: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:25:19: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 08:25:19: 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 08:25:19: Process for pairing-model is terminated! cat: ERX1174070.10_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): 3 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `ERX1174070.10_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 `ERX1174070.10_*.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 `ERX1174070.10_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 @ Fri, 15 Feb 2019 08:25:21: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:25:21: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:25:21: #1 total tags in treatment: 3793768 INFO @ Fri, 15 Feb 2019 08:25:21: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:25:21: #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 08:25:21: #1 tags after filtering in treatment: 3440385 INFO @ Fri, 15 Feb 2019 08:25:21: #1 Redundant rate of treatment: 0.09 INFO @ Fri, 15 Feb 2019 08:25:21: #1 finished! INFO @ Fri, 15 Feb 2019 08:25:21: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:25:21: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:25:22: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 08:25:22: 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 08:25:22: Process for pairing-model is terminated! cat: ERX1174070.20_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): 3 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `ERX1174070.20_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 `ERX1174070.20_*.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 `ERX1174070.20_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。