Job ID = 11192687 sra ファイルのダウンロード中... Completed: 8001K bytes transferred in 2 seconds (24184K 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 255360 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1924808/SRR3824839.sra Written 255360 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1924808/SRR3824839.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: 00:00:08 255360 reads; of these: 255360 (100.00%) were paired; of these: 77421 (30.32%) aligned concordantly 0 times 170573 (66.80%) aligned concordantly exactly 1 time 7366 (2.88%) aligned concordantly >1 times ---- 77421 pairs aligned concordantly 0 times; of these: 11219 (14.49%) aligned discordantly 1 time ---- 66202 pairs aligned 0 times concordantly or discordantly; of these: 132404 mates make up the pairs; of these: 70358 (53.14%) aligned 0 times 58375 (44.09%) aligned exactly 1 time 3671 (2.77%) aligned >1 times 86.22% overall alignment rate Time searching: 00:00:08 Overall time: 00:00:08 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] 45294 / 183807 = 0.2464 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 09:45:51: # Command line: callpeak -t SRX1924808.bam -f BAM -g 12100000 -n SRX1924808.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX1924808.20 # format = BAM # ChIP-seq file = ['SRX1924808.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 09:45:51: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:45:51: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:45:51: # Command line: callpeak -t SRX1924808.bam -f BAM -g 12100000 -n SRX1924808.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX1924808.05 # format = BAM # ChIP-seq file = ['SRX1924808.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 09:45:51: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:45:51: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:45:51: # Command line: callpeak -t SRX1924808.bam -f BAM -g 12100000 -n SRX1924808.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX1924808.10 # format = BAM # ChIP-seq file = ['SRX1924808.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 09:45:51: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:45:51: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:45:53: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 09:45:53: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 09:45:53: #1 total tags in treatment: 133567 INFO @ Sat, 15 Sep 2018 09:45:53: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:45:53: #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 09:45:53: #1 tags after filtering in treatment: 129244 INFO @ Sat, 15 Sep 2018 09:45:53: #1 Redundant rate of treatment: 0.03 INFO @ Sat, 15 Sep 2018 09:45:53: #1 finished! INFO @ Sat, 15 Sep 2018 09:45:53: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:45:53: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:45:53: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 09:45:53: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 09:45:53: #1 total tags in treatment: 133567 INFO @ Sat, 15 Sep 2018 09:45:53: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:45:53: #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 09:45:53: #1 tags after filtering in treatment: 129244 INFO @ Sat, 15 Sep 2018 09:45:53: #1 Redundant rate of treatment: 0.03 INFO @ Sat, 15 Sep 2018 09:45:53: #1 finished! INFO @ Sat, 15 Sep 2018 09:45:53: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:45:53: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:45:53: #2 number of paired peaks: 183 WARNING @ Sat, 15 Sep 2018 09:45:53: Fewer paired peaks (183) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 183 pairs to build model! INFO @ Sat, 15 Sep 2018 09:45:53: start model_add_line... INFO @ Sat, 15 Sep 2018 09:45:53: start X-correlation... INFO @ Sat, 15 Sep 2018 09:45:53: #1 tag size is determined as 40 bps INFO @ Sat, 15 Sep 2018 09:45:53: #1 tag size = 40 INFO @ Sat, 15 Sep 2018 09:45:53: #1 total tags in treatment: 133567 INFO @ Sat, 15 Sep 2018 09:45:53: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:45:53: #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 09:45:53: end of X-cor INFO @ Sat, 15 Sep 2018 09:45:53: #2 finished! INFO @ Sat, 15 Sep 2018 09:45:53: #2 predicted fragment length is 292 bps INFO @ Sat, 15 Sep 2018 09:45:53: #2 alternative fragment length(s) may be 79,154,212,245,263,292,374 bps INFO @ Sat, 15 Sep 2018 09:45:53: #2.2 Generate R script for model : SRX1924808.20_model.r INFO @ Sat, 15 Sep 2018 09:45:53: #1 tags after filtering in treatment: 129244 INFO @ Sat, 15 Sep 2018 09:45:53: #1 Redundant rate of treatment: 0.03 INFO @ Sat, 15 Sep 2018 09:45:53: #1 finished! INFO @ Sat, 15 Sep 2018 09:45:53: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:45:53: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:45:53: #3 Call peaks... INFO @ Sat, 15 Sep 2018 09:45:53: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Sep 2018 09:45:53: #2 number of paired peaks: 183 WARNING @ Sat, 15 Sep 2018 09:45:53: Fewer paired peaks (183) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 183 pairs to build model! INFO @ Sat, 15 Sep 2018 09:45:53: start model_add_line... INFO @ Sat, 15 Sep 2018 09:45:53: start X-correlation... INFO @ Sat, 15 Sep 2018 09:45:53: end of X-cor INFO @ Sat, 15 Sep 2018 09:45:53: #2 finished! INFO @ Sat, 15 Sep 2018 09:45:53: #2 predicted fragment length is 292 bps INFO @ Sat, 15 Sep 2018 09:45:53: #2 alternative fragment length(s) may be 79,154,212,245,263,292,374 bps INFO @ Sat, 15 Sep 2018 09:45:53: #2.2 Generate R script for model : SRX1924808.05_model.r INFO @ Sat, 15 Sep 2018 09:45:53: #2 number of paired peaks: 183 INFO @ Sat, 15 Sep 2018 09:45:53: #3 Call peaks... WARNING @ Sat, 15 Sep 2018 09:45:53: Fewer paired peaks (183) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 183 pairs to build model! INFO @ Sat, 15 Sep 2018 09:45:53: start model_add_line... INFO @ Sat, 15 Sep 2018 09:45:53: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Sep 2018 09:45:53: start X-correlation... INFO @ Sat, 15 Sep 2018 09:45:53: end of X-cor INFO @ Sat, 15 Sep 2018 09:45:53: #2 finished! INFO @ Sat, 15 Sep 2018 09:45:53: #2 predicted fragment length is 292 bps INFO @ Sat, 15 Sep 2018 09:45:53: #2 alternative fragment length(s) may be 79,154,212,245,263,292,374 bps INFO @ Sat, 15 Sep 2018 09:45:53: #2.2 Generate R script for model : SRX1924808.10_model.r INFO @ Sat, 15 Sep 2018 09:45:53: #3 Call peaks... INFO @ Sat, 15 Sep 2018 09:45:53: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Sep 2018 09:45:53: #3 Call peaks for each chromosome... INFO @ Sat, 15 Sep 2018 09:45:53: #3 Call peaks for each chromosome... INFO @ Sat, 15 Sep 2018 09:45:53: #3 Call peaks for each chromosome... INFO @ Sat, 15 Sep 2018 09:45:53: #4 Write output xls file... SRX1924808.20_peaks.xls INFO @ Sat, 15 Sep 2018 09:45:53: #4 Write peak in narrowPeak format file... SRX1924808.20_peaks.narrowPeak INFO @ Sat, 15 Sep 2018 09:45:53: #4 Write summits bed file... SRX1924808.20_summits.bed INFO @ Sat, 15 Sep 2018 09:45:53: Done! INFO @ Sat, 15 Sep 2018 09:45:53: #4 Write output xls file... SRX1924808.10_peaks.xls INFO @ Sat, 15 Sep 2018 09:45:53: #4 Write peak in narrowPeak format file... SRX1924808.10_peaks.narrowPeak INFO @ Sat, 15 Sep 2018 09:45:53: #4 Write summits bed file... SRX1924808.10_summits.bed INFO @ Sat, 15 Sep 2018 09:45:53: Done! INFO @ Sat, 15 Sep 2018 09:45:53: #4 Write output xls file... SRX1924808.05_peaks.xls INFO @ Sat, 15 Sep 2018 09:45:53: #4 Write peak in narrowPeak format file... SRX1924808.05_peaks.narrowPeak INFO @ Sat, 15 Sep 2018 09:45:53: #4 Write summits bed file... SRX1924808.05_summits.bed INFO @ Sat, 15 Sep 2018 09:45:53: Done! pass1 - making usageList (3 chroms): 1 millis pass1 - making usageList (0 chroms): 1 millis pass2 - checking and writing primary data (3 records, 4 fields): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling CompletedMACS2peakCalling pass1 - making usageList (16 chroms): 0 millis pass2 - checking and writing primary data (152 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。