Job ID = 11192940 sra ファイルのダウンロード中... Completed: 363684K bytes transferred in 6 seconds (463909K 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 9948985 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3242055/SRR6129607.sra Written 9948985 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3242055/SRR6129607.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: 00:01:47 9948985 reads; of these: 9948985 (100.00%) were paired; of these: 9630581 (96.80%) aligned concordantly 0 times 258007 (2.59%) aligned concordantly exactly 1 time 60397 (0.61%) aligned concordantly >1 times ---- 9630581 pairs aligned concordantly 0 times; of these: 157601 (1.64%) aligned discordantly 1 time ---- 9472980 pairs aligned 0 times concordantly or discordantly; of these: 18945960 mates make up the pairs; of these: 17945640 (94.72%) aligned 0 times 823678 (4.35%) aligned exactly 1 time 176642 (0.93%) aligned >1 times 9.81% overall alignment rate Time searching: 00:01:47 Overall time: 00:01:47 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] 114043 / 472316 = 0.2415 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 10:36:45: # Command line: callpeak -t SRX3242055.bam -f BAM -g 12100000 -n SRX3242055.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3242055.05 # format = BAM # ChIP-seq file = ['SRX3242055.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 10:36:45: #1 read tag files... INFO @ Sat, 15 Sep 2018 10:36:45: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 10:36:45: # Command line: callpeak -t SRX3242055.bam -f BAM -g 12100000 -n SRX3242055.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3242055.10 # format = BAM # ChIP-seq file = ['SRX3242055.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 10:36:45: #1 read tag files... INFO @ Sat, 15 Sep 2018 10:36:45: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 10:36:45: # Command line: callpeak -t SRX3242055.bam -f BAM -g 12100000 -n SRX3242055.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3242055.20 # format = BAM # ChIP-seq file = ['SRX3242055.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 10:36:45: #1 read tag files... INFO @ Sat, 15 Sep 2018 10:36:45: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 10:36:50: 1000000 INFO @ Sat, 15 Sep 2018 10:36:50: 1000000 INFO @ Sat, 15 Sep 2018 10:36:50: 1000000 INFO @ Sat, 15 Sep 2018 10:36:54: #1 tag size is determined as 42 bps INFO @ Sat, 15 Sep 2018 10:36:54: #1 tag size = 42 INFO @ Sat, 15 Sep 2018 10:36:54: #1 total tags in treatment: 266332 INFO @ Sat, 15 Sep 2018 10:36:54: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 10:36:54: #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 10:36:54: #1 tags after filtering in treatment: 249204 INFO @ Sat, 15 Sep 2018 10:36:54: #1 Redundant rate of treatment: 0.06 INFO @ Sat, 15 Sep 2018 10:36:54: #1 finished! INFO @ Sat, 15 Sep 2018 10:36:54: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 10:36:54: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 10:36:54: #2 number of paired peaks: 155 WARNING @ Sat, 15 Sep 2018 10:36:54: Fewer paired peaks (155) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 155 pairs to build model! INFO @ Sat, 15 Sep 2018 10:36:54: start model_add_line... INFO @ Sat, 15 Sep 2018 10:36:54: start X-correlation... INFO @ Sat, 15 Sep 2018 10:36:54: end of X-cor INFO @ Sat, 15 Sep 2018 10:36:54: #2 finished! INFO @ Sat, 15 Sep 2018 10:36:54: #2 predicted fragment length is 180 bps INFO @ Sat, 15 Sep 2018 10:36:54: #2 alternative fragment length(s) may be 4,161,180,229,541,569 bps INFO @ Sat, 15 Sep 2018 10:36:54: #2.2 Generate R script for model : SRX3242055.05_model.r INFO @ Sat, 15 Sep 2018 10:36:54: #3 Call peaks... INFO @ Sat, 15 Sep 2018 10:36:54: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Sep 2018 10:36:54: #1 tag size is determined as 42 bps INFO @ Sat, 15 Sep 2018 10:36:54: #1 tag size = 42 INFO @ Sat, 15 Sep 2018 10:36:54: #1 total tags in treatment: 266332 INFO @ Sat, 15 Sep 2018 10:36:54: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 10:36:54: #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 10:36:54: #1 tags after filtering in treatment: 249204 INFO @ Sat, 15 Sep 2018 10:36:54: #1 Redundant rate of treatment: 0.06 INFO @ Sat, 15 Sep 2018 10:36:54: #1 finished! INFO @ Sat, 15 Sep 2018 10:36:54: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 10:36:54: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 10:36:54: #1 tag size is determined as 42 bps INFO @ Sat, 15 Sep 2018 10:36:54: #1 tag size = 42 INFO @ Sat, 15 Sep 2018 10:36:54: #1 total tags in treatment: 266332 INFO @ Sat, 15 Sep 2018 10:36:54: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 10:36:54: #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 10:36:54: #1 tags after filtering in treatment: 249204 INFO @ Sat, 15 Sep 2018 10:36:54: #1 Redundant rate of treatment: 0.06 INFO @ Sat, 15 Sep 2018 10:36:54: #1 finished! INFO @ Sat, 15 Sep 2018 10:36:54: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 10:36:54: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 10:36:54: #2 number of paired peaks: 155 WARNING @ Sat, 15 Sep 2018 10:36:54: Fewer paired peaks (155) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 155 pairs to build model! INFO @ Sat, 15 Sep 2018 10:36:54: start model_add_line... INFO @ Sat, 15 Sep 2018 10:36:54: start X-correlation... INFO @ Sat, 15 Sep 2018 10:36:54: end of X-cor INFO @ Sat, 15 Sep 2018 10:36:54: #2 finished! INFO @ Sat, 15 Sep 2018 10:36:54: #2 predicted fragment length is 180 bps INFO @ Sat, 15 Sep 2018 10:36:54: #2 alternative fragment length(s) may be 4,161,180,229,541,569 bps INFO @ Sat, 15 Sep 2018 10:36:54: #2.2 Generate R script for model : SRX3242055.10_model.r INFO @ Sat, 15 Sep 2018 10:36:54: #3 Call peaks... INFO @ Sat, 15 Sep 2018 10:36:54: #2 number of paired peaks: 155 WARNING @ Sat, 15 Sep 2018 10:36:54: Fewer paired peaks (155) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 155 pairs to build model! INFO @ Sat, 15 Sep 2018 10:36:54: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Sep 2018 10:36:54: start model_add_line... INFO @ Sat, 15 Sep 2018 10:36:54: start X-correlation... INFO @ Sat, 15 Sep 2018 10:36:54: end of X-cor INFO @ Sat, 15 Sep 2018 10:36:54: #2 finished! INFO @ Sat, 15 Sep 2018 10:36:54: #2 predicted fragment length is 180 bps INFO @ Sat, 15 Sep 2018 10:36:54: #2 alternative fragment length(s) may be 4,161,180,229,541,569 bps INFO @ Sat, 15 Sep 2018 10:36:54: #2.2 Generate R script for model : SRX3242055.20_model.r INFO @ Sat, 15 Sep 2018 10:36:54: #3 Call peaks... INFO @ Sat, 15 Sep 2018 10:36:54: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Sep 2018 10:36:54: #3 Call peaks for each chromosome... INFO @ Sat, 15 Sep 2018 10:36:55: #3 Call peaks for each chromosome... INFO @ Sat, 15 Sep 2018 10:36:55: #3 Call peaks for each chromosome... INFO @ Sat, 15 Sep 2018 10:36:55: #4 Write output xls file... SRX3242055.05_peaks.xls INFO @ Sat, 15 Sep 2018 10:36:55: #4 Write peak in narrowPeak format file... SRX3242055.05_peaks.narrowPeak INFO @ Sat, 15 Sep 2018 10:36:55: #4 Write summits bed file... SRX3242055.05_summits.bed INFO @ Sat, 15 Sep 2018 10:36:55: Done! pass1 - making usageList (17 chroms): 1 millis pass2 - checking and writing primary data (73 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Sat, 15 Sep 2018 10:36:55: #4 Write output xls file... SRX3242055.10_peaks.xls INFO @ Sat, 15 Sep 2018 10:36:55: #4 Write peak in narrowPeak format file... SRX3242055.10_peaks.narrowPeak INFO @ Sat, 15 Sep 2018 10:36:55: #4 Write summits bed file... SRX3242055.10_summits.bed INFO @ Sat, 15 Sep 2018 10:36:55: Done! pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (39 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Sat, 15 Sep 2018 10:36:55: #4 Write output xls file... SRX3242055.20_peaks.xls INFO @ Sat, 15 Sep 2018 10:36:55: #4 Write peak in narrowPeak format file... SRX3242055.20_peaks.narrowPeak INFO @ Sat, 15 Sep 2018 10:36:55: #4 Write summits bed file... SRX3242055.20_summits.bed INFO @ Sat, 15 Sep 2018 10:36:55: Done! pass1 - making usageList (12 chroms): 0 millis pass2 - checking and writing primary data (24 records, 4 fields): 2 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。