Job ID = 9160024 sra ファイルのダウンロード中... Completed: 31937K bytes transferred in 3 seconds (70071K 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 1087143 spots for /home/okishinya/chipatlas/results/sacCer3/SRX2574964/SRR5270913.sra Written 1087143 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: 00:00:46 1087143 reads; of these: 1087143 (100.00%) were paired; of these: 145409 (13.38%) aligned concordantly 0 times 493400 (45.39%) aligned concordantly exactly 1 time 448334 (41.24%) aligned concordantly >1 times ---- 145409 pairs aligned concordantly 0 times; of these: 6769 (4.66%) aligned discordantly 1 time ---- 138640 pairs aligned 0 times concordantly or discordantly; of these: 277280 mates make up the pairs; of these: 238306 (85.94%) aligned 0 times 15681 (5.66%) aligned exactly 1 time 23293 (8.40%) aligned >1 times 89.04% overall alignment rate Time searching: 00:00:46 Overall time: 00:00:46 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] 43722 / 944977 = 0.0463 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 01:41:24: # Command line: callpeak -t SRX2574964.bam -f BAM -g 12100000 -n SRX2574964.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX2574964.05 # format = BAM # ChIP-seq file = ['SRX2574964.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 01:41:24: #1 read tag files... INFO @ Wed, 28 Jun 2017 01:41:24: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 01:41:24: # Command line: callpeak -t SRX2574964.bam -f BAM -g 12100000 -n SRX2574964.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX2574964.20 # format = BAM # ChIP-seq file = ['SRX2574964.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 01:41:24: #1 read tag files... INFO @ Wed, 28 Jun 2017 01:41:24: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 01:41:24: # Command line: callpeak -t SRX2574964.bam -f BAM -g 12100000 -n SRX2574964.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX2574964.10 # format = BAM # ChIP-seq file = ['SRX2574964.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 01:41:24: #1 read tag files... INFO @ Wed, 28 Jun 2017 01:41:24: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 01:41:29: 1000000 INFO @ Wed, 28 Jun 2017 01:41:29: 1000000 INFO @ Wed, 28 Jun 2017 01:41:29: 1000000 INFO @ Wed, 28 Jun 2017 01:41:34: #1 tag size is determined as 26 bps INFO @ Wed, 28 Jun 2017 01:41:34: #1 tag size = 26 INFO @ Wed, 28 Jun 2017 01:41:34: #1 total tags in treatment: 898042 INFO @ Wed, 28 Jun 2017 01:41:34: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 01:41:34: #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 01:41:34: #1 tag size is determined as 26 bps INFO @ Wed, 28 Jun 2017 01:41:34: #1 tag size = 26 INFO @ Wed, 28 Jun 2017 01:41:34: #1 total tags in treatment: 898042 INFO @ Wed, 28 Jun 2017 01:41:34: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 01:41:34: #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 01:41:34: #1 tags after filtering in treatment: 553573 INFO @ Wed, 28 Jun 2017 01:41:34: #1 Redundant rate of treatment: 0.38 INFO @ Wed, 28 Jun 2017 01:41:34: #1 finished! INFO @ Wed, 28 Jun 2017 01:41:34: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 01:41:34: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 01:41:34: #1 tags after filtering in treatment: 553573 INFO @ Wed, 28 Jun 2017 01:41:34: #1 Redundant rate of treatment: 0.38 INFO @ Wed, 28 Jun 2017 01:41:34: #1 finished! INFO @ Wed, 28 Jun 2017 01:41:34: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 01:41:34: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 01:41:34: #1 tag size is determined as 26 bps INFO @ Wed, 28 Jun 2017 01:41:34: #1 tag size = 26 INFO @ Wed, 28 Jun 2017 01:41:34: #1 total tags in treatment: 898042 INFO @ Wed, 28 Jun 2017 01:41:34: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 01:41:34: #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 01:41:34: #1 tags after filtering in treatment: 553573 INFO @ Wed, 28 Jun 2017 01:41:34: #1 Redundant rate of treatment: 0.38 INFO @ Wed, 28 Jun 2017 01:41:34: #1 finished! INFO @ Wed, 28 Jun 2017 01:41:34: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 01:41:34: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 01:41:34: #2 number of paired peaks: 173 WARNING @ Wed, 28 Jun 2017 01:41:34: Fewer paired peaks (173) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 173 pairs to build model! INFO @ Wed, 28 Jun 2017 01:41:34: start model_add_line... INFO @ Wed, 28 Jun 2017 01:41:34: #2 number of paired peaks: 173 WARNING @ Wed, 28 Jun 2017 01:41:34: Fewer paired peaks (173) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 173 pairs to build model! INFO @ Wed, 28 Jun 2017 01:41:34: start model_add_line... INFO @ Wed, 28 Jun 2017 01:41:34: start X-correlation... INFO @ Wed, 28 Jun 2017 01:41:34: end of X-cor INFO @ Wed, 28 Jun 2017 01:41:34: #2 finished! INFO @ Wed, 28 Jun 2017 01:41:34: #2 predicted fragment length is 221 bps INFO @ Wed, 28 Jun 2017 01:41:34: #2 alternative fragment length(s) may be 221 bps INFO @ Wed, 28 Jun 2017 01:41:34: #2.2 Generate R script for model : SRX2574964.10_model.r INFO @ Wed, 28 Jun 2017 01:41:34: start X-correlation... INFO @ Wed, 28 Jun 2017 01:41:34: end of X-cor INFO @ Wed, 28 Jun 2017 01:41:34: #2 finished! INFO @ Wed, 28 Jun 2017 01:41:34: #2 predicted fragment length is 221 bps INFO @ Wed, 28 Jun 2017 01:41:34: #2 alternative fragment length(s) may be 221 bps INFO @ Wed, 28 Jun 2017 01:41:34: #2.2 Generate R script for model : SRX2574964.20_model.r INFO @ Wed, 28 Jun 2017 01:41:34: #3 Call peaks... INFO @ Wed, 28 Jun 2017 01:41:34: #3 Pre-compute pvalue-qvalue table... INFO @ Wed, 28 Jun 2017 01:41:34: #3 Call peaks... INFO @ Wed, 28 Jun 2017 01:41:34: #3 Pre-compute pvalue-qvalue table... INFO @ Wed, 28 Jun 2017 01:41:34: #2 number of paired peaks: 173 WARNING @ Wed, 28 Jun 2017 01:41:34: Fewer paired peaks (173) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 173 pairs to build model! INFO @ Wed, 28 Jun 2017 01:41:34: start model_add_line... INFO @ Wed, 28 Jun 2017 01:41:34: start X-correlation... INFO @ Wed, 28 Jun 2017 01:41:34: end of X-cor INFO @ Wed, 28 Jun 2017 01:41:34: #2 finished! INFO @ Wed, 28 Jun 2017 01:41:34: #2 predicted fragment length is 221 bps INFO @ Wed, 28 Jun 2017 01:41:34: #2 alternative fragment length(s) may be 221 bps INFO @ Wed, 28 Jun 2017 01:41:34: #2.2 Generate R script for model : SRX2574964.05_model.r INFO @ Wed, 28 Jun 2017 01:41:34: #3 Call peaks... INFO @ Wed, 28 Jun 2017 01:41:34: #3 Pre-compute pvalue-qvalue table... INFO @ Wed, 28 Jun 2017 01:41:36: #3 Call peaks for each chromosome... INFO @ Wed, 28 Jun 2017 01:41:36: #3 Call peaks for each chromosome... INFO @ Wed, 28 Jun 2017 01:41:36: #3 Call peaks for each chromosome... INFO @ Wed, 28 Jun 2017 01:41:36: #4 Write output xls file... SRX2574964.10_peaks.xls INFO @ Wed, 28 Jun 2017 01:41:36: #4 Write peak in narrowPeak format file... SRX2574964.10_peaks.narrowPeak INFO @ Wed, 28 Jun 2017 01:41:36: #4 Write summits bed file... SRX2574964.10_summits.bed INFO @ Wed, 28 Jun 2017 01:41:36: Done! pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (402 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Wed, 28 Jun 2017 01:41:36: #4 Write output xls file... SRX2574964.20_peaks.xls INFO @ Wed, 28 Jun 2017 01:41:36: #4 Write peak in narrowPeak format file... SRX2574964.20_peaks.narrowPeak INFO @ Wed, 28 Jun 2017 01:41:36: #4 Write summits bed file... SRX2574964.20_summits.bed INFO @ Wed, 28 Jun 2017 01:41:36: Done! INFO @ Wed, 28 Jun 2017 01:41:36: #4 Write output xls file... SRX2574964.05_peaks.xls INFO @ Wed, 28 Jun 2017 01:41:36: #4 Write peak in narrowPeak format file... SRX2574964.05_peaks.narrowPeak INFO @ Wed, 28 Jun 2017 01:41:36: #4 Write summits bed file... SRX2574964.05_summits.bed INFO @ Wed, 28 Jun 2017 01:41:36: Done! pass1 - making usageList (16 chroms): 0 millis pass2 - checking and writing primary data (185 records, 4 fields): 2 millis CompletedMACS2peakCalling pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (648 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。