Job ID = 9161987 sra ファイルのダウンロード中... Completed: 1102647K bytes transferred in 13 seconds (693245K 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 25344969 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1423719/SRR2931008.sra Written 25344969 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: 00:18:56 25344969 reads; of these: 25344969 (100.00%) were paired; of these: 7398752 (29.19%) aligned concordantly 0 times 15671494 (61.83%) aligned concordantly exactly 1 time 2274723 (8.98%) aligned concordantly >1 times ---- 7398752 pairs aligned concordantly 0 times; of these: 21384 (0.29%) aligned discordantly 1 time ---- 7377368 pairs aligned 0 times concordantly or discordantly; of these: 14754736 mates make up the pairs; of these: 14335525 (97.16%) aligned 0 times 356952 (2.42%) aligned exactly 1 time 62259 (0.42%) aligned >1 times 71.72% overall alignment rate Time searching: 00:18:56 Overall time: 00:18:56 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_sort_core] merging from 16 files... [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] 16466449 / 17959408 = 0.9169 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 05:36:06: # Command line: callpeak -t SRX1423719.bam -f BAM -g 12100000 -n SRX1423719.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX1423719.10 # format = BAM # ChIP-seq file = ['SRX1423719.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 05:36:06: #1 read tag files... INFO @ Wed, 28 Jun 2017 05:36:06: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 05:36:06: # Command line: callpeak -t SRX1423719.bam -f BAM -g 12100000 -n SRX1423719.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX1423719.20 # format = BAM # ChIP-seq file = ['SRX1423719.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 05:36:06: #1 read tag files... INFO @ Wed, 28 Jun 2017 05:36:06: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 05:36:06: # Command line: callpeak -t SRX1423719.bam -f BAM -g 12100000 -n SRX1423719.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX1423719.05 # format = BAM # ChIP-seq file = ['SRX1423719.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 05:36:06: #1 read tag files... INFO @ Wed, 28 Jun 2017 05:36:06: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 05:36:12: 1000000 INFO @ Wed, 28 Jun 2017 05:36:12: 1000000 INFO @ Wed, 28 Jun 2017 05:36:12: 1000000 INFO @ Wed, 28 Jun 2017 05:36:18: 2000000 INFO @ Wed, 28 Jun 2017 05:36:18: 2000000 INFO @ Wed, 28 Jun 2017 05:36:19: 2000000 INFO @ Wed, 28 Jun 2017 05:36:24: 3000000 INFO @ Wed, 28 Jun 2017 05:36:25: 3000000 INFO @ Wed, 28 Jun 2017 05:36:25: 3000000 INFO @ Wed, 28 Jun 2017 05:36:27: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 05:36:27: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 05:36:27: #1 total tags in treatment: 1489235 INFO @ Wed, 28 Jun 2017 05:36:27: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 05:36:27: #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 05:36:27: #1 tags after filtering in treatment: 1305655 INFO @ Wed, 28 Jun 2017 05:36:27: #1 Redundant rate of treatment: 0.12 INFO @ Wed, 28 Jun 2017 05:36:27: #1 finished! INFO @ Wed, 28 Jun 2017 05:36:27: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 05:36:27: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 05:36:27: #2 number of paired peaks: 306 WARNING @ Wed, 28 Jun 2017 05:36:27: Fewer paired peaks (306) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 306 pairs to build model! INFO @ Wed, 28 Jun 2017 05:36:27: start model_add_line... INFO @ Wed, 28 Jun 2017 05:36:27: start X-correlation... INFO @ Wed, 28 Jun 2017 05:36:27: end of X-cor INFO @ Wed, 28 Jun 2017 05:36:27: #2 finished! INFO @ Wed, 28 Jun 2017 05:36:27: #2 predicted fragment length is 208 bps INFO @ Wed, 28 Jun 2017 05:36:27: #2 alternative fragment length(s) may be 2,156,208 bps INFO @ Wed, 28 Jun 2017 05:36:27: #2.2 Generate R script for model : SRX1423719.10_model.r INFO @ Wed, 28 Jun 2017 05:36:27: #3 Call peaks... INFO @ Wed, 28 Jun 2017 05:36:27: #3 Pre-compute pvalue-qvalue table... INFO @ Wed, 28 Jun 2017 05:36:27: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 05:36:27: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 05:36:27: #1 total tags in treatment: 1489235 INFO @ Wed, 28 Jun 2017 05:36:27: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 05:36:27: #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 05:36:27: #1 tags after filtering in treatment: 1305655 INFO @ Wed, 28 Jun 2017 05:36:27: #1 Redundant rate of treatment: 0.12 INFO @ Wed, 28 Jun 2017 05:36:27: #1 finished! INFO @ Wed, 28 Jun 2017 05:36:27: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 05:36:27: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 05:36:28: #2 number of paired peaks: 306 WARNING @ Wed, 28 Jun 2017 05:36:28: Fewer paired peaks (306) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 306 pairs to build model! INFO @ Wed, 28 Jun 2017 05:36:28: start model_add_line... INFO @ Wed, 28 Jun 2017 05:36:28: start X-correlation... INFO @ Wed, 28 Jun 2017 05:36:28: end of X-cor INFO @ Wed, 28 Jun 2017 05:36:28: #2 finished! INFO @ Wed, 28 Jun 2017 05:36:28: #2 predicted fragment length is 208 bps INFO @ Wed, 28 Jun 2017 05:36:28: #2 alternative fragment length(s) may be 2,156,208 bps INFO @ Wed, 28 Jun 2017 05:36:28: #2.2 Generate R script for model : SRX1423719.05_model.r INFO @ Wed, 28 Jun 2017 05:36:28: #3 Call peaks... INFO @ Wed, 28 Jun 2017 05:36:28: #3 Pre-compute pvalue-qvalue table... INFO @ Wed, 28 Jun 2017 05:36:28: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 05:36:28: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 05:36:28: #1 total tags in treatment: 1489235 INFO @ Wed, 28 Jun 2017 05:36:28: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 05:36:28: #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 05:36:28: #1 tags after filtering in treatment: 1305655 INFO @ Wed, 28 Jun 2017 05:36:28: #1 Redundant rate of treatment: 0.12 INFO @ Wed, 28 Jun 2017 05:36:28: #1 finished! INFO @ Wed, 28 Jun 2017 05:36:28: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 05:36:28: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 05:36:28: #2 number of paired peaks: 306 WARNING @ Wed, 28 Jun 2017 05:36:28: Fewer paired peaks (306) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 306 pairs to build model! INFO @ Wed, 28 Jun 2017 05:36:28: start model_add_line... INFO @ Wed, 28 Jun 2017 05:36:28: start X-correlation... INFO @ Wed, 28 Jun 2017 05:36:28: end of X-cor INFO @ Wed, 28 Jun 2017 05:36:28: #2 finished! INFO @ Wed, 28 Jun 2017 05:36:28: #2 predicted fragment length is 208 bps INFO @ Wed, 28 Jun 2017 05:36:28: #2 alternative fragment length(s) may be 2,156,208 bps INFO @ Wed, 28 Jun 2017 05:36:28: #2.2 Generate R script for model : SRX1423719.20_model.r INFO @ Wed, 28 Jun 2017 05:36:28: #3 Call peaks... INFO @ Wed, 28 Jun 2017 05:36:28: #3 Pre-compute pvalue-qvalue table... INFO @ Wed, 28 Jun 2017 05:36:32: #3 Call peaks for each chromosome... INFO @ Wed, 28 Jun 2017 05:36:33: #3 Call peaks for each chromosome... INFO @ Wed, 28 Jun 2017 05:36:34: #4 Write output xls file... SRX1423719.10_peaks.xls INFO @ Wed, 28 Jun 2017 05:36:34: #4 Write peak in narrowPeak format file... SRX1423719.10_peaks.narrowPeak INFO @ Wed, 28 Jun 2017 05:36:34: #4 Write summits bed file... SRX1423719.10_summits.bed INFO @ Wed, 28 Jun 2017 05:36:34: Done! pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (411 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Wed, 28 Jun 2017 05:36:34: #3 Call peaks for each chromosome... INFO @ Wed, 28 Jun 2017 05:36:34: #4 Write output xls file... SRX1423719.05_peaks.xls INFO @ Wed, 28 Jun 2017 05:36:34: #4 Write peak in narrowPeak format file... SRX1423719.05_peaks.narrowPeak INFO @ Wed, 28 Jun 2017 05:36:34: #4 Write summits bed file... SRX1423719.05_summits.bed INFO @ Wed, 28 Jun 2017 05:36:34: Done! pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (747 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Wed, 28 Jun 2017 05:36:35: #4 Write output xls file... SRX1423719.20_peaks.xls INFO @ Wed, 28 Jun 2017 05:36:35: #4 Write peak in narrowPeak format file... SRX1423719.20_peaks.narrowPeak INFO @ Wed, 28 Jun 2017 05:36:35: #4 Write summits bed file... SRX1423719.20_summits.bed INFO @ Wed, 28 Jun 2017 05:36:35: Done! pass1 - making usageList (15 chroms): 1 millis pass2 - checking and writing primary data (126 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。