Job ID = 11192819 sra ファイルのダウンロード中... Completed: 5848K bytes transferred in 2 seconds (18597K 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 184495 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1924874/SRR3824905.sra Written 184495 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1924874/SRR3824905.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: 00:00:07 184495 reads; of these: 184495 (100.00%) were paired; of these: 59905 (32.47%) aligned concordantly 0 times 119476 (64.76%) aligned concordantly exactly 1 time 5114 (2.77%) aligned concordantly >1 times ---- 59905 pairs aligned concordantly 0 times; of these: 13767 (22.98%) aligned discordantly 1 time ---- 46138 pairs aligned 0 times concordantly or discordantly; of these: 92276 mates make up the pairs; of these: 48550 (52.61%) aligned 0 times 40525 (43.92%) aligned exactly 1 time 3201 (3.47%) aligned >1 times 86.84% overall alignment rate Time searching: 00:00:07 Overall time: 00:00:07 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 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] 32248 / 130687 = 0.2468 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 @ Sat, 15 Sep 2018 09:56:27: # Command line: callpeak -t SRX1924874.bam -f BAM -g 12100000 -n SRX1924874.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX1924874.05 # format = BAM # ChIP-seq file = ['SRX1924874.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 @ Sat, 15 Sep 2018 09:56:27: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:56:27: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:56:27: # Command line: callpeak -t SRX1924874.bam -f BAM -g 12100000 -n SRX1924874.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX1924874.10 # format = BAM # ChIP-seq file = ['SRX1924874.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 @ Sat, 15 Sep 2018 09:56:27: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:56:27: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:56:27: # Command line: callpeak -t SRX1924874.bam -f BAM -g 12100000 -n SRX1924874.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX1924874.20 # format = BAM # ChIP-seq file = ['SRX1924874.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 @ Sat, 15 Sep 2018 09:56:27: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:56:27: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:56:28: #1 tag size is determined as 38 bps INFO @ Sat, 15 Sep 2018 09:56:28: #1 tag size = 38 INFO @ Sat, 15 Sep 2018 09:56:28: #1 total tags in treatment: 93342 INFO @ Sat, 15 Sep 2018 09:56:28: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:56:28: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 09:56:28: #1 tags after filtering in treatment: 91008 INFO @ Sat, 15 Sep 2018 09:56:28: #1 Redundant rate of treatment: 0.03 INFO @ Sat, 15 Sep 2018 09:56:28: #1 finished! INFO @ Sat, 15 Sep 2018 09:56:28: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:56:28: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:56:28: #1 tag size is determined as 38 bps INFO @ Sat, 15 Sep 2018 09:56:28: #1 tag size = 38 INFO @ Sat, 15 Sep 2018 09:56:28: #1 tag size is determined as 38 bps INFO @ Sat, 15 Sep 2018 09:56:28: #1 total tags in treatment: 93342 INFO @ Sat, 15 Sep 2018 09:56:28: #1 tag size = 38 INFO @ Sat, 15 Sep 2018 09:56:28: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:56:28: #1 total tags in treatment: 93342 INFO @ Sat, 15 Sep 2018 09:56:28: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 09:56:28: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:56:28: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 09:56:28: #1 tags after filtering in treatment: 91008 INFO @ Sat, 15 Sep 2018 09:56:28: #1 Redundant rate of treatment: 0.03 INFO @ Sat, 15 Sep 2018 09:56:28: #1 finished! INFO @ Sat, 15 Sep 2018 09:56:28: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:56:28: #1 tags after filtering in treatment: 91008 INFO @ Sat, 15 Sep 2018 09:56:28: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:56:28: #1 Redundant rate of treatment: 0.03 INFO @ Sat, 15 Sep 2018 09:56:28: #1 finished! INFO @ Sat, 15 Sep 2018 09:56:28: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:56:28: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:56:28: #2 number of paired peaks: 229 WARNING @ Sat, 15 Sep 2018 09:56:28: Fewer paired peaks (229) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 229 pairs to build model! INFO @ Sat, 15 Sep 2018 09:56:28: start model_add_line... INFO @ Sat, 15 Sep 2018 09:56:28: start X-correlation... INFO @ Sat, 15 Sep 2018 09:56:28: end of X-cor INFO @ Sat, 15 Sep 2018 09:56:28: #2 finished! INFO @ Sat, 15 Sep 2018 09:56:28: #2 predicted fragment length is 296 bps INFO @ Sat, 15 Sep 2018 09:56:28: #2 alternative fragment length(s) may be 156,229,246,296,350,435 bps INFO @ Sat, 15 Sep 2018 09:56:28: #2.2 Generate R script for model : SRX1924874.20_model.r INFO @ Sat, 15 Sep 2018 09:56:28: #3 Call peaks... INFO @ Sat, 15 Sep 2018 09:56:28: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Sep 2018 09:56:28: #2 number of paired peaks: 229 WARNING @ Sat, 15 Sep 2018 09:56:28: Fewer paired peaks (229) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 229 pairs to build model! INFO @ Sat, 15 Sep 2018 09:56:28: start model_add_line... INFO @ Sat, 15 Sep 2018 09:56:28: #2 number of paired peaks: 229 WARNING @ Sat, 15 Sep 2018 09:56:28: Fewer paired peaks (229) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 229 pairs to build model! INFO @ Sat, 15 Sep 2018 09:56:28: start model_add_line... INFO @ Sat, 15 Sep 2018 09:56:28: start X-correlation... INFO @ Sat, 15 Sep 2018 09:56:28: start X-correlation... INFO @ Sat, 15 Sep 2018 09:56:28: end of X-cor INFO @ Sat, 15 Sep 2018 09:56:28: end of X-cor INFO @ Sat, 15 Sep 2018 09:56:28: #2 finished! INFO @ Sat, 15 Sep 2018 09:56:28: #2 finished! INFO @ Sat, 15 Sep 2018 09:56:28: #2 predicted fragment length is 296 bps INFO @ Sat, 15 Sep 2018 09:56:28: #2 predicted fragment length is 296 bps INFO @ Sat, 15 Sep 2018 09:56:28: #2 alternative fragment length(s) may be 156,229,246,296,350,435 bps INFO @ Sat, 15 Sep 2018 09:56:28: #2 alternative fragment length(s) may be 156,229,246,296,350,435 bps INFO @ Sat, 15 Sep 2018 09:56:28: #2.2 Generate R script for model : SRX1924874.05_model.r INFO @ Sat, 15 Sep 2018 09:56:28: #2.2 Generate R script for model : SRX1924874.10_model.r INFO @ Sat, 15 Sep 2018 09:56:28: #3 Call peaks... INFO @ Sat, 15 Sep 2018 09:56:28: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Sep 2018 09:56:28: #3 Call peaks... INFO @ Sat, 15 Sep 2018 09:56:28: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Sep 2018 09:56:29: #3 Call peaks for each chromosome... INFO @ Sat, 15 Sep 2018 09:56:29: #3 Call peaks for each chromosome... INFO @ Sat, 15 Sep 2018 09:56:29: #3 Call peaks for each chromosome... INFO @ Sat, 15 Sep 2018 09:56:29: #4 Write output xls file... SRX1924874.20_peaks.xls INFO @ Sat, 15 Sep 2018 09:56:29: #4 Write peak in narrowPeak format file... SRX1924874.20_peaks.narrowPeak INFO @ Sat, 15 Sep 2018 09:56:29: #4 Write summits bed file... SRX1924874.20_summits.bed INFO @ Sat, 15 Sep 2018 09:56:29: Done! INFO @ Sat, 15 Sep 2018 09:56:29: #4 Write output xls file... SRX1924874.10_peaks.xls INFO @ Sat, 15 Sep 2018 09:56:29: #4 Write peak in narrowPeak format file... SRX1924874.10_peaks.narrowPeak INFO @ Sat, 15 Sep 2018 09:56:29: #4 Write summits bed file... SRX1924874.10_summits.bed INFO @ Sat, 15 Sep 2018 09:56:29: Done! INFO @ Sat, 15 Sep 2018 09:56:29: #4 Write output xls file... SRX1924874.05_peaks.xls INFO @ Sat, 15 Sep 2018 09:56:29: #4 Write peak in narrowPeak format file... SRX1924874.05_peaks.narrowPeak INFO @ Sat, 15 Sep 2018 09:56:29: #4 Write summits bed file... SRX1924874.05_summits.bed INFO @ Sat, 15 Sep 2018 09:56:29: Done! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling pass1 - making usageList (1 chroms): 1 millis pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (1 records, 4 fields): 1 millis pass2 - checking and writing primary data (39 records, 4 fields): 2 millis CompletedMACS2peakCalling CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。