Job ID = 11633390 sra ファイルのダウンロード中... Completed: 113276K bytes transferred in 4 seconds (216971K 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 1904824 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1236168/ERR1162761.sra Written 1904824 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1236168/ERR1162761.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: 00:01:27 1904824 reads; of these: 1904824 (100.00%) were paired; of these: 232983 (12.23%) aligned concordantly 0 times 1487852 (78.11%) aligned concordantly exactly 1 time 183989 (9.66%) aligned concordantly >1 times ---- 232983 pairs aligned concordantly 0 times; of these: 63332 (27.18%) aligned discordantly 1 time ---- 169651 pairs aligned 0 times concordantly or discordantly; of these: 339302 mates make up the pairs; of these: 312537 (92.11%) aligned 0 times 9559 (2.82%) aligned exactly 1 time 17206 (5.07%) aligned >1 times 91.80% overall alignment rate Time searching: 00:01:27 Overall time: 00:01:27 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] 63583 / 1734240 = 0.0367 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 @ Fri, 15 Feb 2019 08:53:30: # Command line: callpeak -t ERX1236168.bam -f BAM -g 12100000 -n ERX1236168.05 -q 1e-05 # ARGUMENTS LIST: # name = ERX1236168.05 # format = BAM # ChIP-seq file = ['ERX1236168.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 @ Fri, 15 Feb 2019 08:53:30: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:53:30: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:53:30: # Command line: callpeak -t ERX1236168.bam -f BAM -g 12100000 -n ERX1236168.10 -q 1e-10 # ARGUMENTS LIST: # name = ERX1236168.10 # format = BAM # ChIP-seq file = ['ERX1236168.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 @ Fri, 15 Feb 2019 08:53:30: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:53:30: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:53:30: # Command line: callpeak -t ERX1236168.bam -f BAM -g 12100000 -n ERX1236168.20 -q 1e-20 # ARGUMENTS LIST: # name = ERX1236168.20 # format = BAM # ChIP-seq file = ['ERX1236168.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 @ Fri, 15 Feb 2019 08:53:30: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:53:30: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:53:36: 1000000 INFO @ Fri, 15 Feb 2019 08:53:36: 1000000 INFO @ Fri, 15 Feb 2019 08:53:36: 1000000 INFO @ Fri, 15 Feb 2019 08:53:42: 2000000 INFO @ Fri, 15 Feb 2019 08:53:42: 2000000 INFO @ Fri, 15 Feb 2019 08:53:43: 2000000 INFO @ Fri, 15 Feb 2019 08:53:48: 3000000 INFO @ Fri, 15 Feb 2019 08:53:49: 3000000 INFO @ Fri, 15 Feb 2019 08:53:49: 3000000 INFO @ Fri, 15 Feb 2019 08:53:51: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:53:51: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:53:51: #1 total tags in treatment: 1610598 INFO @ Fri, 15 Feb 2019 08:53:51: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:53:51: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 08:53:51: #1 tags after filtering in treatment: 1439074 INFO @ Fri, 15 Feb 2019 08:53:51: #1 Redundant rate of treatment: 0.11 INFO @ Fri, 15 Feb 2019 08:53:51: #1 finished! INFO @ Fri, 15 Feb 2019 08:53:51: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:53:51: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:53:51: #2 number of paired peaks: 145 WARNING @ Fri, 15 Feb 2019 08:53:51: Fewer paired peaks (145) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 145 pairs to build model! INFO @ Fri, 15 Feb 2019 08:53:51: start model_add_line... INFO @ Fri, 15 Feb 2019 08:53:51: start X-correlation... INFO @ Fri, 15 Feb 2019 08:53:51: end of X-cor INFO @ Fri, 15 Feb 2019 08:53:51: #2 finished! INFO @ Fri, 15 Feb 2019 08:53:51: #2 predicted fragment length is 251 bps INFO @ Fri, 15 Feb 2019 08:53:51: #2 alternative fragment length(s) may be 4,251 bps INFO @ Fri, 15 Feb 2019 08:53:51: #2.2 Generate R script for model : ERX1236168.10_model.r INFO @ Fri, 15 Feb 2019 08:53:51: #3 Call peaks... INFO @ Fri, 15 Feb 2019 08:53:51: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 08:53:51: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:53:51: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:53:51: #1 total tags in treatment: 1610598 INFO @ Fri, 15 Feb 2019 08:53:51: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:53:51: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 08:53:51: #1 tags after filtering in treatment: 1439074 INFO @ Fri, 15 Feb 2019 08:53:51: #1 Redundant rate of treatment: 0.11 INFO @ Fri, 15 Feb 2019 08:53:51: #1 finished! INFO @ Fri, 15 Feb 2019 08:53:51: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:53:51: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:53:51: #2 number of paired peaks: 145 WARNING @ Fri, 15 Feb 2019 08:53:51: Fewer paired peaks (145) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 145 pairs to build model! INFO @ Fri, 15 Feb 2019 08:53:51: start model_add_line... INFO @ Fri, 15 Feb 2019 08:53:51: start X-correlation... INFO @ Fri, 15 Feb 2019 08:53:51: end of X-cor INFO @ Fri, 15 Feb 2019 08:53:51: #2 finished! INFO @ Fri, 15 Feb 2019 08:53:51: #2 predicted fragment length is 251 bps INFO @ Fri, 15 Feb 2019 08:53:51: #2 alternative fragment length(s) may be 4,251 bps INFO @ Fri, 15 Feb 2019 08:53:51: #2.2 Generate R script for model : ERX1236168.05_model.r INFO @ Fri, 15 Feb 2019 08:53:51: #3 Call peaks... INFO @ Fri, 15 Feb 2019 08:53:51: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 08:53:52: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:53:52: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:53:52: #1 total tags in treatment: 1610598 INFO @ Fri, 15 Feb 2019 08:53:52: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:53:52: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 08:53:52: #1 tags after filtering in treatment: 1439074 INFO @ Fri, 15 Feb 2019 08:53:52: #1 Redundant rate of treatment: 0.11 INFO @ Fri, 15 Feb 2019 08:53:52: #1 finished! INFO @ Fri, 15 Feb 2019 08:53:52: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:53:52: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:53:52: #2 number of paired peaks: 145 WARNING @ Fri, 15 Feb 2019 08:53:52: Fewer paired peaks (145) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 145 pairs to build model! INFO @ Fri, 15 Feb 2019 08:53:52: start model_add_line... INFO @ Fri, 15 Feb 2019 08:53:52: start X-correlation... INFO @ Fri, 15 Feb 2019 08:53:52: end of X-cor INFO @ Fri, 15 Feb 2019 08:53:52: #2 finished! INFO @ Fri, 15 Feb 2019 08:53:52: #2 predicted fragment length is 251 bps INFO @ Fri, 15 Feb 2019 08:53:52: #2 alternative fragment length(s) may be 4,251 bps INFO @ Fri, 15 Feb 2019 08:53:52: #2.2 Generate R script for model : ERX1236168.20_model.r INFO @ Fri, 15 Feb 2019 08:53:52: #3 Call peaks... INFO @ Fri, 15 Feb 2019 08:53:52: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 08:53:55: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 08:53:56: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 08:53:57: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 08:53:57: #4 Write output xls file... ERX1236168.10_peaks.xls INFO @ Fri, 15 Feb 2019 08:53:57: #4 Write peak in narrowPeak format file... ERX1236168.10_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 08:53:57: #4 Write summits bed file... ERX1236168.10_summits.bed INFO @ Fri, 15 Feb 2019 08:53:57: Done! pass1 - making usageList (16 chroms): 2 millis pass2 - checking and writing primary data (118 records, 4 fields): 4 millis CompletedMACS2peakCalling INFO @ Fri, 15 Feb 2019 08:53:58: #4 Write output xls file... ERX1236168.05_peaks.xls INFO @ Fri, 15 Feb 2019 08:53:58: #4 Write peak in narrowPeak format file... ERX1236168.05_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 08:53:58: #4 Write summits bed file... ERX1236168.05_summits.bed INFO @ Fri, 15 Feb 2019 08:53:58: Done! pass1 - making usageList (17 chroms): 2 millis pass2 - checking and writing primary data (228 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Fri, 15 Feb 2019 08:53:58: #4 Write output xls file... ERX1236168.20_peaks.xls INFO @ Fri, 15 Feb 2019 08:53:58: #4 Write peak in narrowPeak format file... ERX1236168.20_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 08:53:58: #4 Write summits bed file... ERX1236168.20_summits.bed INFO @ Fri, 15 Feb 2019 08:53:58: Done! pass1 - making usageList (12 chroms): 1 millis pass2 - checking and writing primary data (44 records, 4 fields): 3 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。