Job ID = 11244998 sra ファイルのダウンロード中... Completed: 308281K bytes transferred in 8 seconds (304472K 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 9153029 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4554711/SRR7696384.sra Written 9153029 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4554711/SRR7696384.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: 00:04:32 9153029 reads; of these: 9153029 (100.00%) were paired; of these: 4900562 (53.54%) aligned concordantly 0 times 3681816 (40.23%) aligned concordantly exactly 1 time 570651 (6.23%) aligned concordantly >1 times ---- 4900562 pairs aligned concordantly 0 times; of these: 2276 (0.05%) aligned discordantly 1 time ---- 4898286 pairs aligned 0 times concordantly or discordantly; of these: 9796572 mates make up the pairs; of these: 5856194 (59.78%) aligned 0 times 3451059 (35.23%) aligned exactly 1 time 489319 (4.99%) aligned >1 times 68.01% overall alignment rate Time searching: 00:04:32 Overall time: 00:04:32 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] 356547 / 4254189 = 0.0838 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 @ Tue, 09 Oct 2018 23:11:48: # Command line: callpeak -t SRX4554711.bam -f BAM -g 12100000 -n SRX4554711.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX4554711.05 # format = BAM # ChIP-seq file = ['SRX4554711.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 @ Tue, 09 Oct 2018 23:11:48: #1 read tag files... INFO @ Tue, 09 Oct 2018 23:11:48: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 23:11:48: # Command line: callpeak -t SRX4554711.bam -f BAM -g 12100000 -n SRX4554711.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX4554711.20 # format = BAM # ChIP-seq file = ['SRX4554711.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 @ Tue, 09 Oct 2018 23:11:48: #1 read tag files... INFO @ Tue, 09 Oct 2018 23:11:48: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 23:11:48: # Command line: callpeak -t SRX4554711.bam -f BAM -g 12100000 -n SRX4554711.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX4554711.10 # format = BAM # ChIP-seq file = ['SRX4554711.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 @ Tue, 09 Oct 2018 23:11:48: #1 read tag files... INFO @ Tue, 09 Oct 2018 23:11:48: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 23:11:53: 1000000 INFO @ Tue, 09 Oct 2018 23:11:53: 1000000 INFO @ Tue, 09 Oct 2018 23:11:53: 1000000 INFO @ Tue, 09 Oct 2018 23:11:58: 2000000 INFO @ Tue, 09 Oct 2018 23:11:59: 2000000 INFO @ Tue, 09 Oct 2018 23:11:59: 2000000 INFO @ Tue, 09 Oct 2018 23:12:04: 3000000 INFO @ Tue, 09 Oct 2018 23:12:04: 3000000 INFO @ Tue, 09 Oct 2018 23:12:04: 3000000 INFO @ Tue, 09 Oct 2018 23:12:09: 4000000 INFO @ Tue, 09 Oct 2018 23:12:09: 4000000 INFO @ Tue, 09 Oct 2018 23:12:09: 4000000 INFO @ Tue, 09 Oct 2018 23:12:14: 5000000 INFO @ Tue, 09 Oct 2018 23:12:14: 5000000 INFO @ Tue, 09 Oct 2018 23:12:14: 5000000 INFO @ Tue, 09 Oct 2018 23:12:19: 6000000 INFO @ Tue, 09 Oct 2018 23:12:19: 6000000 INFO @ Tue, 09 Oct 2018 23:12:20: 6000000 INFO @ Tue, 09 Oct 2018 23:12:24: 7000000 INFO @ Tue, 09 Oct 2018 23:12:25: 7000000 INFO @ Tue, 09 Oct 2018 23:12:25: 7000000 INFO @ Tue, 09 Oct 2018 23:12:30: 8000000 INFO @ Tue, 09 Oct 2018 23:12:30: 8000000 INFO @ Tue, 09 Oct 2018 23:12:31: 8000000 INFO @ Tue, 09 Oct 2018 23:12:35: 9000000 INFO @ Tue, 09 Oct 2018 23:12:36: 9000000 INFO @ Tue, 09 Oct 2018 23:12:37: 9000000 INFO @ Tue, 09 Oct 2018 23:12:41: 10000000 INFO @ Tue, 09 Oct 2018 23:12:42: 10000000 INFO @ Tue, 09 Oct 2018 23:12:42: 10000000 INFO @ Tue, 09 Oct 2018 23:12:47: 11000000 INFO @ Tue, 09 Oct 2018 23:12:48: 11000000 INFO @ Tue, 09 Oct 2018 23:12:48: 11000000 INFO @ Tue, 09 Oct 2018 23:12:51: #1 tag size is determined as 37 bps INFO @ Tue, 09 Oct 2018 23:12:51: #1 tag size = 37 INFO @ Tue, 09 Oct 2018 23:12:51: #1 total tags in treatment: 3895930 INFO @ Tue, 09 Oct 2018 23:12:51: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 23:12:51: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 09 Oct 2018 23:12:51: #1 tags after filtering in treatment: 2317264 INFO @ Tue, 09 Oct 2018 23:12:51: #1 Redundant rate of treatment: 0.41 INFO @ Tue, 09 Oct 2018 23:12:51: #1 finished! INFO @ Tue, 09 Oct 2018 23:12:51: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 23:12:51: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 23:12:51: #2 number of paired peaks: 25 WARNING @ Tue, 09 Oct 2018 23:12:51: Too few paired peaks (25) 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 @ Tue, 09 Oct 2018 23:12:51: Process for pairing-model is terminated! cat: SRX4554711.05_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 `SRX4554711.05_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 `SRX4554711.05_*.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 `SRX4554711.05_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 @ Tue, 09 Oct 2018 23:12:52: #1 tag size is determined as 37 bps INFO @ Tue, 09 Oct 2018 23:12:52: #1 tag size = 37 INFO @ Tue, 09 Oct 2018 23:12:52: #1 total tags in treatment: 3895930 INFO @ Tue, 09 Oct 2018 23:12:52: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 23:12:52: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 09 Oct 2018 23:12:52: #1 tags after filtering in treatment: 2317264 INFO @ Tue, 09 Oct 2018 23:12:52: #1 Redundant rate of treatment: 0.41 INFO @ Tue, 09 Oct 2018 23:12:52: #1 finished! INFO @ Tue, 09 Oct 2018 23:12:52: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 23:12:52: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 23:12:52: #2 number of paired peaks: 25 WARNING @ Tue, 09 Oct 2018 23:12:52: Too few paired peaks (25) 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 @ Tue, 09 Oct 2018 23:12:52: Process for pairing-model is terminated! cat: SRX4554711.20_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 `SRX4554711.20_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 `SRX4554711.20_*.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 `SRX4554711.20_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 @ Tue, 09 Oct 2018 23:12:52: #1 tag size is determined as 37 bps INFO @ Tue, 09 Oct 2018 23:12:52: #1 tag size = 37 INFO @ Tue, 09 Oct 2018 23:12:52: #1 total tags in treatment: 3895930 INFO @ Tue, 09 Oct 2018 23:12:52: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 23:12:52: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 09 Oct 2018 23:12:53: #1 tags after filtering in treatment: 2317264 INFO @ Tue, 09 Oct 2018 23:12:53: #1 Redundant rate of treatment: 0.41 INFO @ Tue, 09 Oct 2018 23:12:53: #1 finished! INFO @ Tue, 09 Oct 2018 23:12:53: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 23:12:53: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 23:12:53: #2 number of paired peaks: 25 WARNING @ Tue, 09 Oct 2018 23:12:53: Too few paired peaks (25) 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 @ Tue, 09 Oct 2018 23:12:53: Process for pairing-model is terminated! cat: SRX4554711.10_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 `SRX4554711.10_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 `SRX4554711.10_*.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 `SRX4554711.10_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。