Job ID = 11193154 sra ファイルのダウンロード中... Completed: 416427K bytes transferred in 30 seconds (112703K 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 12247252 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4337746/SRR7467857.sra Written 12247252 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4337746/SRR7467857.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: 00:03:29 12247252 reads; of these: 12247252 (100.00%) were paired; of these: 11746685 (95.91%) aligned concordantly 0 times 455203 (3.72%) aligned concordantly exactly 1 time 45364 (0.37%) aligned concordantly >1 times ---- 11746685 pairs aligned concordantly 0 times; of these: 515785 (4.39%) aligned discordantly 1 time ---- 11230900 pairs aligned 0 times concordantly or discordantly; of these: 22461800 mates make up the pairs; of these: 18881009 (84.06%) aligned 0 times 3224023 (14.35%) aligned exactly 1 time 356768 (1.59%) aligned >1 times 22.92% overall alignment rate Time searching: 00:03:29 Overall time: 00:03:29 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] 688295 / 1012526 = 0.6798 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 11:07:39: # Command line: callpeak -t SRX4337746.bam -f BAM -g 12100000 -n SRX4337746.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX4337746.20 # format = BAM # ChIP-seq file = ['SRX4337746.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 11:07:39: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:07:39: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:07:39: # Command line: callpeak -t SRX4337746.bam -f BAM -g 12100000 -n SRX4337746.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX4337746.10 # format = BAM # ChIP-seq file = ['SRX4337746.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 11:07:39: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:07:39: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:07:39: # Command line: callpeak -t SRX4337746.bam -f BAM -g 12100000 -n SRX4337746.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX4337746.05 # format = BAM # ChIP-seq file = ['SRX4337746.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 11:07:39: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:07:39: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:07:45: 1000000 INFO @ Sat, 15 Sep 2018 11:07:45: 1000000 INFO @ Sat, 15 Sep 2018 11:07:45: 1000000 INFO @ Sat, 15 Sep 2018 11:07:50: 2000000 INFO @ Sat, 15 Sep 2018 11:07:50: 2000000 INFO @ Sat, 15 Sep 2018 11:07:50: 2000000 INFO @ Sat, 15 Sep 2018 11:07:56: 3000000 INFO @ Sat, 15 Sep 2018 11:07:56: 3000000 INFO @ Sat, 15 Sep 2018 11:07:56: 3000000 INFO @ Sat, 15 Sep 2018 11:08:03: 4000000 INFO @ Sat, 15 Sep 2018 11:08:03: 4000000 INFO @ Sat, 15 Sep 2018 11:08:03: 4000000 INFO @ Sat, 15 Sep 2018 11:08:04: #1 tag size is determined as 45 bps INFO @ Sat, 15 Sep 2018 11:08:04: #1 tag size is determined as 45 bps INFO @ Sat, 15 Sep 2018 11:08:04: #1 tag size = 45 INFO @ Sat, 15 Sep 2018 11:08:04: #1 tag size = 45 INFO @ Sat, 15 Sep 2018 11:08:04: #1 total tags in treatment: 265835 INFO @ Sat, 15 Sep 2018 11:08:04: #1 total tags in treatment: 265835 INFO @ Sat, 15 Sep 2018 11:08:04: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:08:04: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:08:04: #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 11:08:04: #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 11:08:04: #1 tag size is determined as 45 bps INFO @ Sat, 15 Sep 2018 11:08:04: #1 tag size = 45 INFO @ Sat, 15 Sep 2018 11:08:04: #1 total tags in treatment: 265835 INFO @ Sat, 15 Sep 2018 11:08:04: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:08:04: #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 11:08:04: #1 tags after filtering in treatment: 249059 INFO @ Sat, 15 Sep 2018 11:08:04: #1 tags after filtering in treatment: 249059 INFO @ Sat, 15 Sep 2018 11:08:04: #1 Redundant rate of treatment: 0.06 INFO @ Sat, 15 Sep 2018 11:08:04: #1 Redundant rate of treatment: 0.06 INFO @ Sat, 15 Sep 2018 11:08:04: #1 finished! INFO @ Sat, 15 Sep 2018 11:08:04: #1 finished! INFO @ Sat, 15 Sep 2018 11:08:04: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:08:04: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:08:04: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:08:04: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:08:04: #1 tags after filtering in treatment: 249059 INFO @ Sat, 15 Sep 2018 11:08:04: #1 Redundant rate of treatment: 0.06 INFO @ Sat, 15 Sep 2018 11:08:04: #1 finished! INFO @ Sat, 15 Sep 2018 11:08:04: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:08:04: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:08:04: #2 number of paired peaks: 71 WARNING @ Sat, 15 Sep 2018 11:08:04: Too few paired peaks (71) 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 11:08:04: Process for pairing-model is terminated! INFO @ Sat, 15 Sep 2018 11:08:04: #2 number of paired peaks: 71 WARNING @ Sat, 15 Sep 2018 11:08:04: Too few paired peaks (71) 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 11:08:04: Process for pairing-model is terminated! INFO @ Sat, 15 Sep 2018 11:08:04: #2 number of paired peaks: 71 WARNING @ Sat, 15 Sep 2018 11:08:04: Too few paired peaks (71) 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 11:08:04: Process for pairing-model is terminated! cat: SRX4337746.20_peaks.narrowPeakcat: SRX4337746.05_peaks.narrowPeak: そのようなファイルやディレクトリはありません : そのようなファイルやディレクトリはありません cat: SRX4337746.10_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 pass1 - making usageList (0 chroms): 1 millis pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) needLargeMem: trying to allocate 0 bytes (limit: 17179869184) needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4337746.05_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 `SRX4337746.20_model.r'rm: : そのようなファイルやディレクトリはありませんcannot remove `SRX4337746.05_*.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 `SRX4337746.20_*.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 `SRX4337746.10_model.r'rm: cannot remove `SRX4337746.05_peaks.narrowPeak': そのようなファイルやディレクトリはありません : 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 `SRX4337746.20_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 CompletedMACS2peakCalling rm: cannot remove `SRX4337746.10_*.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 `SRX4337746.10_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。