Job ID = 11633517 sra ファイルのダウンロード中... Completed: 119130K bytes transferred in 4 seconds (225762K 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 1778318 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1236294/ERR1162887.sra Written 1778318 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1236294/ERR1162887.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: 00:01:28 1778318 reads; of these: 1778318 (100.00%) were paired; of these: 150719 (8.48%) aligned concordantly 0 times 1463566 (82.30%) aligned concordantly exactly 1 time 164033 (9.22%) aligned concordantly >1 times ---- 150719 pairs aligned concordantly 0 times; of these: 32120 (21.31%) aligned discordantly 1 time ---- 118599 pairs aligned 0 times concordantly or discordantly; of these: 237198 mates make up the pairs; of these: 218282 (92.03%) aligned 0 times 10564 (4.45%) aligned exactly 1 time 8352 (3.52%) aligned >1 times 93.86% overall alignment rate Time searching: 00:01:28 Overall time: 00:01:28 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] 742050 / 1657935 = 0.4476 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 09:01:17: # Command line: callpeak -t ERX1236294.bam -f BAM -g 12100000 -n ERX1236294.20 -q 1e-20 # ARGUMENTS LIST: # name = ERX1236294.20 # format = BAM # ChIP-seq file = ['ERX1236294.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 09:01:17: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:01:17: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:01:17: # Command line: callpeak -t ERX1236294.bam -f BAM -g 12100000 -n ERX1236294.05 -q 1e-05 # ARGUMENTS LIST: # name = ERX1236294.05 # format = BAM # ChIP-seq file = ['ERX1236294.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 09:01:17: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:01:17: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:01:17: # Command line: callpeak -t ERX1236294.bam -f BAM -g 12100000 -n ERX1236294.10 -q 1e-10 # ARGUMENTS LIST: # name = ERX1236294.10 # format = BAM # ChIP-seq file = ['ERX1236294.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 09:01:17: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:01:17: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:01:23: 1000000 INFO @ Fri, 15 Feb 2019 09:01:23: 1000000 INFO @ Fri, 15 Feb 2019 09:01:23: 1000000 INFO @ Fri, 15 Feb 2019 09:01:28: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:01:28: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:01:28: #1 total tags in treatment: 894318 INFO @ Fri, 15 Feb 2019 09:01:28: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:01:28: #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 09:01:28: #1 tags after filtering in treatment: 839431 INFO @ Fri, 15 Feb 2019 09:01:28: #1 Redundant rate of treatment: 0.06 INFO @ Fri, 15 Feb 2019 09:01:28: #1 finished! INFO @ Fri, 15 Feb 2019 09:01:28: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:01:28: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:01:28: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:01:28: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:01:28: #1 total tags in treatment: 894318 INFO @ Fri, 15 Feb 2019 09:01:28: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:01:28: #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 09:01:28: #2 number of paired peaks: 278 WARNING @ Fri, 15 Feb 2019 09:01:28: Fewer paired peaks (278) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 278 pairs to build model! INFO @ Fri, 15 Feb 2019 09:01:28: start model_add_line... INFO @ Fri, 15 Feb 2019 09:01:28: start X-correlation... INFO @ Fri, 15 Feb 2019 09:01:28: #1 tags after filtering in treatment: 839431 INFO @ Fri, 15 Feb 2019 09:01:28: #1 Redundant rate of treatment: 0.06 INFO @ Fri, 15 Feb 2019 09:01:28: #1 finished! INFO @ Fri, 15 Feb 2019 09:01:28: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:01:28: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:01:28: end of X-cor INFO @ Fri, 15 Feb 2019 09:01:28: #2 finished! INFO @ Fri, 15 Feb 2019 09:01:28: #2 predicted fragment length is 197 bps INFO @ Fri, 15 Feb 2019 09:01:28: #2 alternative fragment length(s) may be 4,171,179,197 bps INFO @ Fri, 15 Feb 2019 09:01:28: #2.2 Generate R script for model : ERX1236294.10_model.r INFO @ Fri, 15 Feb 2019 09:01:28: #3 Call peaks... INFO @ Fri, 15 Feb 2019 09:01:28: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 09:01:28: #2 number of paired peaks: 278 WARNING @ Fri, 15 Feb 2019 09:01:28: Fewer paired peaks (278) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 278 pairs to build model! INFO @ Fri, 15 Feb 2019 09:01:28: start model_add_line... INFO @ Fri, 15 Feb 2019 09:01:28: start X-correlation... INFO @ Fri, 15 Feb 2019 09:01:28: end of X-cor INFO @ Fri, 15 Feb 2019 09:01:28: #2 finished! INFO @ Fri, 15 Feb 2019 09:01:28: #2 predicted fragment length is 197 bps INFO @ Fri, 15 Feb 2019 09:01:28: #2 alternative fragment length(s) may be 4,171,179,197 bps INFO @ Fri, 15 Feb 2019 09:01:28: #2.2 Generate R script for model : ERX1236294.20_model.r INFO @ Fri, 15 Feb 2019 09:01:28: #3 Call peaks... INFO @ Fri, 15 Feb 2019 09:01:28: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 09:01:29: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:01:29: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:01:29: #1 total tags in treatment: 894318 INFO @ Fri, 15 Feb 2019 09:01:29: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:01:29: #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 09:01:29: #1 tags after filtering in treatment: 839431 INFO @ Fri, 15 Feb 2019 09:01:29: #1 Redundant rate of treatment: 0.06 INFO @ Fri, 15 Feb 2019 09:01:29: #1 finished! INFO @ Fri, 15 Feb 2019 09:01:29: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:01:29: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:01:29: #2 number of paired peaks: 278 WARNING @ Fri, 15 Feb 2019 09:01:29: Fewer paired peaks (278) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 278 pairs to build model! INFO @ Fri, 15 Feb 2019 09:01:29: start model_add_line... INFO @ Fri, 15 Feb 2019 09:01:29: start X-correlation... INFO @ Fri, 15 Feb 2019 09:01:29: end of X-cor INFO @ Fri, 15 Feb 2019 09:01:29: #2 finished! INFO @ Fri, 15 Feb 2019 09:01:29: #2 predicted fragment length is 197 bps INFO @ Fri, 15 Feb 2019 09:01:29: #2 alternative fragment length(s) may be 4,171,179,197 bps INFO @ Fri, 15 Feb 2019 09:01:29: #2.2 Generate R script for model : ERX1236294.05_model.r INFO @ Fri, 15 Feb 2019 09:01:29: #3 Call peaks... INFO @ Fri, 15 Feb 2019 09:01:29: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 09:01:31: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 09:01:31: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 09:01:32: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 09:01:32: #4 Write output xls file... ERX1236294.20_peaks.xls INFO @ Fri, 15 Feb 2019 09:01:32: #4 Write peak in narrowPeak format file... ERX1236294.20_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 09:01:32: #4 Write summits bed file... ERX1236294.20_summits.bed INFO @ Fri, 15 Feb 2019 09:01:32: Done! INFO @ Fri, 15 Feb 2019 09:01:32: #4 Write output xls file... ERX1236294.10_peaks.xls INFO @ Fri, 15 Feb 2019 09:01:32: #4 Write peak in narrowPeak format file... ERX1236294.10_peaks.narrowPeak pass1 - making usageList (16 chroms): 2 millis pass2 - checking and writing primary data (200 records, 4 fields): 4 millis INFO @ Fri, 15 Feb 2019 09:01:32: #4 Write summits bed file... ERX1236294.10_summits.bed INFO @ Fri, 15 Feb 2019 09:01:32: Done! CompletedMACS2peakCalling pass1 - making usageList (16 chroms): 6 millis pass2 - checking and writing primary data (344 records, 4 fields): 4 millis CompletedMACS2peakCalling INFO @ Fri, 15 Feb 2019 09:01:33: #4 Write output xls file... ERX1236294.05_peaks.xls INFO @ Fri, 15 Feb 2019 09:01:33: #4 Write peak in narrowPeak format file... ERX1236294.05_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 09:01:33: #4 Write summits bed file... ERX1236294.05_summits.bed INFO @ Fri, 15 Feb 2019 09:01:33: Done! pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (612 records, 4 fields): 4 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。