Job ID = 11192771 sra ファイルのダウンロード中... Completed: 64733K bytes transferred in 4 seconds (126064K 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 2090865 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1924887/SRR3824918.sra Written 2090865 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1924887/SRR3824918.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: 00:01:15 2090865 reads; of these: 2090865 (100.00%) were paired; of these: 262288 (12.54%) aligned concordantly 0 times 1720106 (82.27%) aligned concordantly exactly 1 time 108471 (5.19%) aligned concordantly >1 times ---- 262288 pairs aligned concordantly 0 times; of these: 92876 (35.41%) aligned discordantly 1 time ---- 169412 pairs aligned 0 times concordantly or discordantly; of these: 338824 mates make up the pairs; of these: 232909 (68.74%) aligned 0 times 87300 (25.77%) aligned exactly 1 time 18615 (5.49%) aligned >1 times 94.43% overall alignment rate Time searching: 00:01:15 Overall time: 00:01:15 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] 400285 / 1898514 = 0.2108 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 09:55:06: # Command line: callpeak -t SRX1924887.bam -f BAM -g 12100000 -n SRX1924887.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX1924887.10 # format = BAM # ChIP-seq file = ['SRX1924887.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 09:55:06: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:55:06: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:55:06: # Command line: callpeak -t SRX1924887.bam -f BAM -g 12100000 -n SRX1924887.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX1924887.20 # format = BAM # ChIP-seq file = ['SRX1924887.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 09:55:06: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:55:06: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:55:06: # Command line: callpeak -t SRX1924887.bam -f BAM -g 12100000 -n SRX1924887.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX1924887.05 # format = BAM # ChIP-seq file = ['SRX1924887.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 09:55:06: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:55:06: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:55:11: 1000000 INFO @ Sat, 15 Sep 2018 09:55:11: 1000000 INFO @ Sat, 15 Sep 2018 09:55:11: 1000000 INFO @ Sat, 15 Sep 2018 09:55:16: 2000000 INFO @ Sat, 15 Sep 2018 09:55:16: 2000000 INFO @ Sat, 15 Sep 2018 09:55:16: 2000000 INFO @ Sat, 15 Sep 2018 09:55:21: 3000000 INFO @ Sat, 15 Sep 2018 09:55:21: 3000000 INFO @ Sat, 15 Sep 2018 09:55:22: 3000000 INFO @ Sat, 15 Sep 2018 09:55:22: #1 tag size is determined as 38 bps INFO @ Sat, 15 Sep 2018 09:55:22: #1 tag size = 38 INFO @ Sat, 15 Sep 2018 09:55:22: #1 total tags in treatment: 1436633 INFO @ Sat, 15 Sep 2018 09:55:22: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:55:22: #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 09:55:22: #1 tags after filtering in treatment: 1200204 INFO @ Sat, 15 Sep 2018 09:55:22: #1 Redundant rate of treatment: 0.16 INFO @ Sat, 15 Sep 2018 09:55:22: #1 finished! INFO @ Sat, 15 Sep 2018 09:55:22: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:55:22: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:55:22: #2 number of paired peaks: 0 WARNING @ Sat, 15 Sep 2018 09:55:22: 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 @ Sat, 15 Sep 2018 09:55:22: Process for pairing-model is terminated! cat: SRX1924887.20_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): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX1924887.20_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 `SRX1924887.20_*.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 `SRX1924887.20_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 09:55:22: #1 tag size is determined as 38 bps INFO @ Sat, 15 Sep 2018 09:55:22: #1 tag size = 38 INFO @ Sat, 15 Sep 2018 09:55:22: #1 total tags in treatment: 1436633 INFO @ Sat, 15 Sep 2018 09:55:22: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:55:22: #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 09:55:22: #1 tags after filtering in treatment: 1200204 INFO @ Sat, 15 Sep 2018 09:55:22: #1 Redundant rate of treatment: 0.16 INFO @ Sat, 15 Sep 2018 09:55:22: #1 finished! INFO @ Sat, 15 Sep 2018 09:55:22: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:55:22: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:55:22: #2 number of paired peaks: 0 WARNING @ Sat, 15 Sep 2018 09:55:22: 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 @ Sat, 15 Sep 2018 09:55:22: Process for pairing-model is terminated! cat: SRX1924887.05_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): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX1924887.05_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 `SRX1924887.05_*.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 `SRX1924887.05_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 09:55:22: #1 tag size is determined as 38 bps INFO @ Sat, 15 Sep 2018 09:55:22: #1 tag size = 38 INFO @ Sat, 15 Sep 2018 09:55:22: #1 total tags in treatment: 1436633 INFO @ Sat, 15 Sep 2018 09:55:22: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:55:22: #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 09:55:22: #1 tags after filtering in treatment: 1200204 INFO @ Sat, 15 Sep 2018 09:55:22: #1 Redundant rate of treatment: 0.16 INFO @ Sat, 15 Sep 2018 09:55:22: #1 finished! INFO @ Sat, 15 Sep 2018 09:55:22: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:55:22: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:55:22: #2 number of paired peaks: 0 WARNING @ Sat, 15 Sep 2018 09:55:22: 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 @ Sat, 15 Sep 2018 09:55:22: Process for pairing-model is terminated! cat: SRX1924887.10_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 `SRX1924887.10_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 `SRX1924887.10_*.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 `SRX1924887.10_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。