Job ID = 9161939 sra ファイルのダウンロード中... Completed: 229314K bytes transferred in 5 seconds (329240K bits/sec), in 1 file, 2 directories. 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... Written 3351780 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1419790/SRR2927539.sra Written 3351780 spots total 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: 00:03:53 3351780 reads; of these: 3351780 (100.00%) were paired; of these: 259400 (7.74%) aligned concordantly 0 times 2746177 (81.93%) aligned concordantly exactly 1 time 346203 (10.33%) aligned concordantly >1 times ---- 259400 pairs aligned concordantly 0 times; of these: 66345 (25.58%) aligned discordantly 1 time ---- 193055 pairs aligned 0 times concordantly or discordantly; of these: 386110 mates make up the pairs; of these: 346001 (89.61%) aligned 0 times 17151 (4.44%) aligned exactly 1 time 22958 (5.95%) aligned >1 times 94.84% overall alignment rate Time searching: 00:03:53 Overall time: 00:03:53 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] 83375 / 3153791 = 0.0264 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 @ Wed, 28 Jun 2017 05:07:11: # Command line: callpeak -t SRX1419790.bam -f BAM -g 12100000 -n SRX1419790.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX1419790.20 # format = BAM # ChIP-seq file = ['SRX1419790.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 @ Wed, 28 Jun 2017 05:07:11: #1 read tag files... INFO @ Wed, 28 Jun 2017 05:07:11: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 05:07:11: # Command line: callpeak -t SRX1419790.bam -f BAM -g 12100000 -n SRX1419790.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX1419790.05 # format = BAM # ChIP-seq file = ['SRX1419790.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 @ Wed, 28 Jun 2017 05:07:11: #1 read tag files... INFO @ Wed, 28 Jun 2017 05:07:11: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 05:07:11: # Command line: callpeak -t SRX1419790.bam -f BAM -g 12100000 -n SRX1419790.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX1419790.10 # format = BAM # ChIP-seq file = ['SRX1419790.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 @ Wed, 28 Jun 2017 05:07:11: #1 read tag files... INFO @ Wed, 28 Jun 2017 05:07:11: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 05:07:20: 1000000 INFO @ Wed, 28 Jun 2017 05:07:20: 1000000 INFO @ Wed, 28 Jun 2017 05:07:20: 1000000 INFO @ Wed, 28 Jun 2017 05:07:28: 2000000 INFO @ Wed, 28 Jun 2017 05:07:29: 2000000 INFO @ Wed, 28 Jun 2017 05:07:29: 2000000 INFO @ Wed, 28 Jun 2017 05:07:37: 3000000 INFO @ Wed, 28 Jun 2017 05:07:37: 3000000 INFO @ Wed, 28 Jun 2017 05:07:37: 3000000 INFO @ Wed, 28 Jun 2017 05:07:46: 4000000 INFO @ Wed, 28 Jun 2017 05:07:46: 4000000 INFO @ Wed, 28 Jun 2017 05:07:46: 4000000 INFO @ Wed, 28 Jun 2017 05:07:54: 5000000 INFO @ Wed, 28 Jun 2017 05:07:55: 5000000 INFO @ Wed, 28 Jun 2017 05:07:55: 5000000 INFO @ Wed, 28 Jun 2017 05:08:03: 6000000 INFO @ Wed, 28 Jun 2017 05:08:03: 6000000 INFO @ Wed, 28 Jun 2017 05:08:03: 6000000 INFO @ Wed, 28 Jun 2017 05:08:04: #1 tag size is determined as 94 bps INFO @ Wed, 28 Jun 2017 05:08:04: #1 tag size = 94 INFO @ Wed, 28 Jun 2017 05:08:04: #1 total tags in treatment: 3009813 INFO @ Wed, 28 Jun 2017 05:08:04: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 05:08:04: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 28 Jun 2017 05:08:04: #1 tags after filtering in treatment: 2582994 INFO @ Wed, 28 Jun 2017 05:08:04: #1 Redundant rate of treatment: 0.14 INFO @ Wed, 28 Jun 2017 05:08:04: #1 finished! INFO @ Wed, 28 Jun 2017 05:08:04: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 05:08:04: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 05:08:05: #2 number of paired peaks: 49 WARNING @ Wed, 28 Jun 2017 05:08:05: Too few paired peaks (49) 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 @ Wed, 28 Jun 2017 05:08:05: Process for pairing-model is terminated! cat: SRX1419790.10_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 needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX1419790.10_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 `SRX1419790.10_*.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 `SRX1419790.10_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 @ Wed, 28 Jun 2017 05:08:05: #1 tag size is determined as 94 bps INFO @ Wed, 28 Jun 2017 05:08:05: #1 tag size = 94 INFO @ Wed, 28 Jun 2017 05:08:05: #1 total tags in treatment: 3009813 INFO @ Wed, 28 Jun 2017 05:08:05: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 05:08:05: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 28 Jun 2017 05:08:05: #1 tag size is determined as 94 bps INFO @ Wed, 28 Jun 2017 05:08:05: #1 tag size = 94 INFO @ Wed, 28 Jun 2017 05:08:05: #1 total tags in treatment: 3009813 INFO @ Wed, 28 Jun 2017 05:08:05: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 05:08:05: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 28 Jun 2017 05:08:05: #1 tags after filtering in treatment: 2582994 INFO @ Wed, 28 Jun 2017 05:08:05: #1 Redundant rate of treatment: 0.14 INFO @ Wed, 28 Jun 2017 05:08:05: #1 finished! INFO @ Wed, 28 Jun 2017 05:08:05: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 05:08:05: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 05:08:05: #1 tags after filtering in treatment: 2582994 INFO @ Wed, 28 Jun 2017 05:08:05: #1 Redundant rate of treatment: 0.14 INFO @ Wed, 28 Jun 2017 05:08:05: #1 finished! INFO @ Wed, 28 Jun 2017 05:08:05: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 05:08:05: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 05:08:05: #2 number of paired peaks: 49 WARNING @ Wed, 28 Jun 2017 05:08:05: Too few paired peaks (49) 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 @ Wed, 28 Jun 2017 05:08:05: Process for pairing-model is terminated! cat: SRX1419790.20_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 `SRX1419790.20_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 `SRX1419790.20_*.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 `SRX1419790.20_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 @ Wed, 28 Jun 2017 05:08:05: #2 number of paired peaks: 49 WARNING @ Wed, 28 Jun 2017 05:08:05: Too few paired peaks (49) 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 @ Wed, 28 Jun 2017 05:08:05: Process for pairing-model is terminated! cat: SRX1419790.05_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 `SRX1419790.05_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 `SRX1419790.05_*.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 `SRX1419790.05_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。