Job ID = 11244868 sra ファイルのダウンロード中... Completed: 479209K bytes transferred in 7 seconds (523367K 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 4950654 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3765660/SRR6807383.sra Written 4950654 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3765660/SRR6807383.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: 00:05:52 4950654 reads; of these: 4950654 (100.00%) were paired; of these: 149929 (3.03%) aligned concordantly 0 times 4337788 (87.62%) aligned concordantly exactly 1 time 462937 (9.35%) aligned concordantly >1 times ---- 149929 pairs aligned concordantly 0 times; of these: 69275 (46.21%) aligned discordantly 1 time ---- 80654 pairs aligned 0 times concordantly or discordantly; of these: 161308 mates make up the pairs; of these: 95337 (59.10%) aligned 0 times 45683 (28.32%) aligned exactly 1 time 20288 (12.58%) aligned >1 times 99.04% overall alignment rate Time searching: 00:05:52 Overall time: 00:05:52 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] 372636 / 4848904 = 0.0768 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 22:23:02: # Command line: callpeak -t SRX3765660.bam -f BAM -g 12100000 -n SRX3765660.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3765660.10 # format = BAM # ChIP-seq file = ['SRX3765660.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 22:23:02: #1 read tag files... INFO @ Tue, 09 Oct 2018 22:23:02: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 22:23:02: # Command line: callpeak -t SRX3765660.bam -f BAM -g 12100000 -n SRX3765660.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3765660.20 # format = BAM # ChIP-seq file = ['SRX3765660.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 22:23:02: #1 read tag files... INFO @ Tue, 09 Oct 2018 22:23:02: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 22:23:02: # Command line: callpeak -t SRX3765660.bam -f BAM -g 12100000 -n SRX3765660.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3765660.05 # format = BAM # ChIP-seq file = ['SRX3765660.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 22:23:02: #1 read tag files... INFO @ Tue, 09 Oct 2018 22:23:02: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 22:23:10: 1000000 INFO @ Tue, 09 Oct 2018 22:23:10: 1000000 INFO @ Tue, 09 Oct 2018 22:23:10: 1000000 INFO @ Tue, 09 Oct 2018 22:23:18: 2000000 INFO @ Tue, 09 Oct 2018 22:23:18: 2000000 INFO @ Tue, 09 Oct 2018 22:23:18: 2000000 INFO @ Tue, 09 Oct 2018 22:23:26: 3000000 INFO @ Tue, 09 Oct 2018 22:23:26: 3000000 INFO @ Tue, 09 Oct 2018 22:23:26: 3000000 INFO @ Tue, 09 Oct 2018 22:23:34: 4000000 INFO @ Tue, 09 Oct 2018 22:23:34: 4000000 INFO @ Tue, 09 Oct 2018 22:23:34: 4000000 INFO @ Tue, 09 Oct 2018 22:23:42: 5000000 INFO @ Tue, 09 Oct 2018 22:23:42: 5000000 INFO @ Tue, 09 Oct 2018 22:23:42: 5000000 INFO @ Tue, 09 Oct 2018 22:23:50: 6000000 INFO @ Tue, 09 Oct 2018 22:23:50: 6000000 INFO @ Tue, 09 Oct 2018 22:23:50: 6000000 INFO @ Tue, 09 Oct 2018 22:23:57: 7000000 INFO @ Tue, 09 Oct 2018 22:23:58: 7000000 INFO @ Tue, 09 Oct 2018 22:23:58: 7000000 INFO @ Tue, 09 Oct 2018 22:24:05: 8000000 INFO @ Tue, 09 Oct 2018 22:24:06: 8000000 INFO @ Tue, 09 Oct 2018 22:24:06: 8000000 INFO @ Tue, 09 Oct 2018 22:24:14: 9000000 INFO @ Tue, 09 Oct 2018 22:24:14: #1 tag size is determined as 101 bps INFO @ Tue, 09 Oct 2018 22:24:14: #1 tag size = 101 INFO @ Tue, 09 Oct 2018 22:24:14: #1 total tags in treatment: 4428654 INFO @ Tue, 09 Oct 2018 22:24:14: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 22:24:14: #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 22:24:14: 9000000 INFO @ Tue, 09 Oct 2018 22:24:14: 9000000 INFO @ Tue, 09 Oct 2018 22:24:15: #1 tags after filtering in treatment: 3075490 INFO @ Tue, 09 Oct 2018 22:24:15: #1 Redundant rate of treatment: 0.31 INFO @ Tue, 09 Oct 2018 22:24:15: #1 finished! INFO @ Tue, 09 Oct 2018 22:24:15: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 22:24:15: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 22:24:15: #2 number of paired peaks: 21 WARNING @ Tue, 09 Oct 2018 22:24:15: Too few paired peaks (21) 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 22:24:15: Process for pairing-model is terminated! cat: SRX3765660.10_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 `SRX3765660.10_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 `SRX3765660.10_*.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 `SRX3765660.10_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 @ Tue, 09 Oct 2018 22:24:15: #1 tag size is determined as 101 bps INFO @ Tue, 09 Oct 2018 22:24:15: #1 tag size = 101 INFO @ Tue, 09 Oct 2018 22:24:15: #1 total tags in treatment: 4428654 INFO @ Tue, 09 Oct 2018 22:24:15: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 22:24:15: #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 22:24:15: #1 tag size is determined as 101 bps INFO @ Tue, 09 Oct 2018 22:24:15: #1 tag size = 101 INFO @ Tue, 09 Oct 2018 22:24:15: #1 total tags in treatment: 4428654 INFO @ Tue, 09 Oct 2018 22:24:15: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 22:24:15: #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 22:24:15: #1 tags after filtering in treatment: 3075490 INFO @ Tue, 09 Oct 2018 22:24:15: #1 Redundant rate of treatment: 0.31 INFO @ Tue, 09 Oct 2018 22:24:15: #1 finished! INFO @ Tue, 09 Oct 2018 22:24:15: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 22:24:15: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 22:24:15: #1 tags after filtering in treatment: 3075490 INFO @ Tue, 09 Oct 2018 22:24:15: #1 Redundant rate of treatment: 0.31 INFO @ Tue, 09 Oct 2018 22:24:15: #1 finished! INFO @ Tue, 09 Oct 2018 22:24:15: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 22:24:15: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 22:24:15: #2 number of paired peaks: 21 WARNING @ Tue, 09 Oct 2018 22:24:15: Too few paired peaks (21) 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 22:24:15: Process for pairing-model is terminated! cat: SRX3765660.20_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 `SRX3765660.20_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 `SRX3765660.20_*.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 `SRX3765660.20_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 22:24:15: #2 number of paired peaks: 21 WARNING @ Tue, 09 Oct 2018 22:24:15: Too few paired peaks (21) 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 22:24:15: Process for pairing-model is terminated! cat: SRX3765660.05_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 `SRX3765660.05_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 `SRX3765660.05_*.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 `SRX3765660.05_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。