Job ID = 11633194 sra ファイルのダウンロード中... Completed: 281687K bytes transferred in 7 seconds (294961K 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/ERX1174130/ERR1094644.sra Written 4000000 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1174130/ERR1094644.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: 00:03:01 4000000 reads; of these: 4000000 (100.00%) were paired; of these: 412988 (10.32%) aligned concordantly 0 times 3338086 (83.45%) aligned concordantly exactly 1 time 248926 (6.22%) aligned concordantly >1 times ---- 412988 pairs aligned concordantly 0 times; of these: 139225 (33.71%) aligned discordantly 1 time ---- 273763 pairs aligned 0 times concordantly or discordantly; of these: 547526 mates make up the pairs; of these: 364955 (66.66%) aligned 0 times 147320 (26.91%) aligned exactly 1 time 35251 (6.44%) aligned >1 times 95.44% overall alignment rate Time searching: 00:03:01 Overall time: 00:03:01 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] 24654 / 3720436 = 0.0066 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 08:47:27: # Command line: callpeak -t ERX1174130.bam -f BAM -g 12100000 -n ERX1174130.10 -q 1e-10 # ARGUMENTS LIST: # name = ERX1174130.10 # format = BAM # ChIP-seq file = ['ERX1174130.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 08:47:27: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:47:27: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:47:27: # Command line: callpeak -t ERX1174130.bam -f BAM -g 12100000 -n ERX1174130.05 -q 1e-05 # ARGUMENTS LIST: # name = ERX1174130.05 # format = BAM # ChIP-seq file = ['ERX1174130.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 08:47:27: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:47:27: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:47:27: # Command line: callpeak -t ERX1174130.bam -f BAM -g 12100000 -n ERX1174130.20 -q 1e-20 # ARGUMENTS LIST: # name = ERX1174130.20 # format = BAM # ChIP-seq file = ['ERX1174130.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 08:47:27: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:47:27: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:47:34: 1000000 INFO @ Fri, 15 Feb 2019 08:47:34: 1000000 INFO @ Fri, 15 Feb 2019 08:47:34: 1000000 INFO @ Fri, 15 Feb 2019 08:47:41: 2000000 INFO @ Fri, 15 Feb 2019 08:47:41: 2000000 INFO @ Fri, 15 Feb 2019 08:47:41: 2000000 INFO @ Fri, 15 Feb 2019 08:47:49: 3000000 INFO @ Fri, 15 Feb 2019 08:47:49: 3000000 INFO @ Fri, 15 Feb 2019 08:47:49: 3000000 INFO @ Fri, 15 Feb 2019 08:47:55: 4000000 INFO @ Fri, 15 Feb 2019 08:47:55: 4000000 INFO @ Fri, 15 Feb 2019 08:47:56: 4000000 INFO @ Fri, 15 Feb 2019 08:48:03: 5000000 INFO @ Fri, 15 Feb 2019 08:48:03: 5000000 INFO @ Fri, 15 Feb 2019 08:48:03: 5000000 INFO @ Fri, 15 Feb 2019 08:48:10: 6000000 INFO @ Fri, 15 Feb 2019 08:48:10: 6000000 INFO @ Fri, 15 Feb 2019 08:48:11: 6000000 INFO @ Fri, 15 Feb 2019 08:48:18: 7000000 INFO @ Fri, 15 Feb 2019 08:48:18: 7000000 INFO @ Fri, 15 Feb 2019 08:48:18: 7000000 INFO @ Fri, 15 Feb 2019 08:48:22: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:48:22: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:48:22: #1 total tags in treatment: 3562700 INFO @ Fri, 15 Feb 2019 08:48:22: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:48:22: #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 08:48:22: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:48:22: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:48:22: #1 total tags in treatment: 3562700 INFO @ Fri, 15 Feb 2019 08:48:22: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:48:22: #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 08:48:22: #1 tags after filtering in treatment: 3251516 INFO @ Fri, 15 Feb 2019 08:48:22: #1 Redundant rate of treatment: 0.09 INFO @ Fri, 15 Feb 2019 08:48:22: #1 finished! INFO @ Fri, 15 Feb 2019 08:48:22: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:48:22: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:48:22: #1 tags after filtering in treatment: 3251516 INFO @ Fri, 15 Feb 2019 08:48:22: #1 Redundant rate of treatment: 0.09 INFO @ Fri, 15 Feb 2019 08:48:22: #1 finished! INFO @ Fri, 15 Feb 2019 08:48:22: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:48:22: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:48:22: #2 number of paired peaks: 2 WARNING @ Fri, 15 Feb 2019 08:48:22: Too few paired peaks (2) 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 08:48:22: Process for pairing-model is terminated! INFO @ Fri, 15 Feb 2019 08:48:22: #2 number of paired peaks: 2 WARNING @ Fri, 15 Feb 2019 08:48:22: Too few paired peaks (2) 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 08:48:22: Process for pairing-model is terminated! cat: ERX1174130.20_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: ERX1174130.10_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): 6 millis pass1 - making usageList (0 chroms): 7 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `ERX1174130.20_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 `ERX1174130.10_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 `ERX1174130.20_*.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 `ERX1174130.10_*.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 `ERX1174130.20_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 `ERX1174130.10_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 CompletedMACS2peakCalling INFO @ Fri, 15 Feb 2019 08:48:22: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:48:22: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:48:22: #1 total tags in treatment: 3562700 INFO @ Fri, 15 Feb 2019 08:48:22: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:48:22: #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 08:48:23: #1 tags after filtering in treatment: 3251516 INFO @ Fri, 15 Feb 2019 08:48:23: #1 Redundant rate of treatment: 0.09 INFO @ Fri, 15 Feb 2019 08:48:23: #1 finished! INFO @ Fri, 15 Feb 2019 08:48:23: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:48:23: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:48:23: #2 number of paired peaks: 2 WARNING @ Fri, 15 Feb 2019 08:48:23: Too few paired peaks (2) 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 08:48:23: Process for pairing-model is terminated! cat: ERX1174130.05_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): 4 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `ERX1174130.05_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 `ERX1174130.05_*.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 `ERX1174130.05_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。