Job ID = 11633395 sra ファイルのダウンロード中... Completed: 229232K bytes transferred in 4 seconds (382631K 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 4000000 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1236172/ERR1162765.sra Written 4000000 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1236172/ERR1162765.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: 00:03:01 4000000 reads; of these: 4000000 (100.00%) were paired; of these: 251472 (6.29%) aligned concordantly 0 times 3433542 (85.84%) aligned concordantly exactly 1 time 314986 (7.87%) aligned concordantly >1 times ---- 251472 pairs aligned concordantly 0 times; of these: 18174 (7.23%) aligned discordantly 1 time ---- 233298 pairs aligned 0 times concordantly or discordantly; of these: 466596 mates make up the pairs; of these: 448742 (96.17%) aligned 0 times 11731 (2.51%) aligned exactly 1 time 6123 (1.31%) aligned >1 times 94.39% overall alignment rate Time searching: 00:03:01 Overall time: 00:03:01 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] 436647 / 3765601 = 0.1160 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 08:57:15: # Command line: callpeak -t ERX1236172.bam -f BAM -g 12100000 -n ERX1236172.20 -q 1e-20 # ARGUMENTS LIST: # name = ERX1236172.20 # format = BAM # ChIP-seq file = ['ERX1236172.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 08:57:15: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:57:15: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:57:15: # Command line: callpeak -t ERX1236172.bam -f BAM -g 12100000 -n ERX1236172.05 -q 1e-05 # ARGUMENTS LIST: # name = ERX1236172.05 # format = BAM # ChIP-seq file = ['ERX1236172.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 08:57:15: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:57:15: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:57:15: # Command line: callpeak -t ERX1236172.bam -f BAM -g 12100000 -n ERX1236172.10 -q 1e-10 # ARGUMENTS LIST: # name = ERX1236172.10 # format = BAM # ChIP-seq file = ['ERX1236172.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 08:57:15: #1 read tag files... INFO @ Fri, 15 Feb 2019 08:57:15: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 08:57:21: 1000000 INFO @ Fri, 15 Feb 2019 08:57:21: 1000000 INFO @ Fri, 15 Feb 2019 08:57:21: 1000000 INFO @ Fri, 15 Feb 2019 08:57:27: 2000000 INFO @ Fri, 15 Feb 2019 08:57:27: 2000000 INFO @ Fri, 15 Feb 2019 08:57:27: 2000000 INFO @ Fri, 15 Feb 2019 08:57:32: 3000000 INFO @ Fri, 15 Feb 2019 08:57:32: 3000000 INFO @ Fri, 15 Feb 2019 08:57:34: 3000000 INFO @ Fri, 15 Feb 2019 08:57:38: 4000000 INFO @ Fri, 15 Feb 2019 08:57:38: 4000000 INFO @ Fri, 15 Feb 2019 08:57:40: 4000000 INFO @ Fri, 15 Feb 2019 08:57:44: 5000000 INFO @ Fri, 15 Feb 2019 08:57:44: 5000000 INFO @ Fri, 15 Feb 2019 08:57:46: 5000000 INFO @ Fri, 15 Feb 2019 08:57:49: 6000000 INFO @ Fri, 15 Feb 2019 08:57:50: 6000000 INFO @ Fri, 15 Feb 2019 08:57:51: 6000000 INFO @ Fri, 15 Feb 2019 08:57:53: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:57:53: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:57:53: #1 total tags in treatment: 3313201 INFO @ Fri, 15 Feb 2019 08:57:53: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:57:53: #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 08:57:53: #1 tags after filtering in treatment: 2456025 INFO @ Fri, 15 Feb 2019 08:57:53: #1 Redundant rate of treatment: 0.26 INFO @ Fri, 15 Feb 2019 08:57:53: #1 finished! INFO @ Fri, 15 Feb 2019 08:57:53: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:57:53: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:57:53: #2 number of paired peaks: 209 WARNING @ Fri, 15 Feb 2019 08:57:53: Fewer paired peaks (209) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 209 pairs to build model! INFO @ Fri, 15 Feb 2019 08:57:53: start model_add_line... INFO @ Fri, 15 Feb 2019 08:57:53: start X-correlation... INFO @ Fri, 15 Feb 2019 08:57:53: end of X-cor INFO @ Fri, 15 Feb 2019 08:57:53: #2 finished! INFO @ Fri, 15 Feb 2019 08:57:53: #2 predicted fragment length is 220 bps INFO @ Fri, 15 Feb 2019 08:57:53: #2 alternative fragment length(s) may be 3,220,235 bps INFO @ Fri, 15 Feb 2019 08:57:53: #2.2 Generate R script for model : ERX1236172.05_model.r INFO @ Fri, 15 Feb 2019 08:57:53: #3 Call peaks... INFO @ Fri, 15 Feb 2019 08:57:53: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 08:57:53: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:57:53: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:57:53: #1 total tags in treatment: 3313201 INFO @ Fri, 15 Feb 2019 08:57:53: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:57:53: #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 08:57:54: #1 tags after filtering in treatment: 2456025 INFO @ Fri, 15 Feb 2019 08:57:54: #1 Redundant rate of treatment: 0.26 INFO @ Fri, 15 Feb 2019 08:57:54: #1 finished! INFO @ Fri, 15 Feb 2019 08:57:54: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:57:54: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:57:54: #2 number of paired peaks: 209 WARNING @ Fri, 15 Feb 2019 08:57:54: Fewer paired peaks (209) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 209 pairs to build model! INFO @ Fri, 15 Feb 2019 08:57:54: start model_add_line... INFO @ Fri, 15 Feb 2019 08:57:54: start X-correlation... INFO @ Fri, 15 Feb 2019 08:57:54: end of X-cor INFO @ Fri, 15 Feb 2019 08:57:54: #2 finished! INFO @ Fri, 15 Feb 2019 08:57:54: #2 predicted fragment length is 220 bps INFO @ Fri, 15 Feb 2019 08:57:54: #2 alternative fragment length(s) may be 3,220,235 bps INFO @ Fri, 15 Feb 2019 08:57:54: #2.2 Generate R script for model : ERX1236172.10_model.r INFO @ Fri, 15 Feb 2019 08:57:54: #3 Call peaks... INFO @ Fri, 15 Feb 2019 08:57:54: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 08:57:54: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 08:57:54: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 08:57:54: #1 total tags in treatment: 3313201 INFO @ Fri, 15 Feb 2019 08:57:54: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 08:57:54: #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 08:57:54: #1 tags after filtering in treatment: 2456025 INFO @ Fri, 15 Feb 2019 08:57:54: #1 Redundant rate of treatment: 0.26 INFO @ Fri, 15 Feb 2019 08:57:54: #1 finished! INFO @ Fri, 15 Feb 2019 08:57:54: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 08:57:54: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 08:57:55: #2 number of paired peaks: 209 WARNING @ Fri, 15 Feb 2019 08:57:55: Fewer paired peaks (209) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 209 pairs to build model! INFO @ Fri, 15 Feb 2019 08:57:55: start model_add_line... INFO @ Fri, 15 Feb 2019 08:57:55: start X-correlation... INFO @ Fri, 15 Feb 2019 08:57:55: end of X-cor INFO @ Fri, 15 Feb 2019 08:57:55: #2 finished! INFO @ Fri, 15 Feb 2019 08:57:55: #2 predicted fragment length is 220 bps INFO @ Fri, 15 Feb 2019 08:57:55: #2 alternative fragment length(s) may be 3,220,235 bps INFO @ Fri, 15 Feb 2019 08:57:55: #2.2 Generate R script for model : ERX1236172.20_model.r INFO @ Fri, 15 Feb 2019 08:57:55: #3 Call peaks... INFO @ Fri, 15 Feb 2019 08:57:55: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 08:58:02: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 08:58:03: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 08:58:03: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 08:58:04: #4 Write output xls file... ERX1236172.05_peaks.xls INFO @ Fri, 15 Feb 2019 08:58:04: #4 Write peak in narrowPeak format file... ERX1236172.05_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 08:58:04: #4 Write summits bed file... ERX1236172.05_summits.bed INFO @ Fri, 15 Feb 2019 08:58:04: Done! pass1 - making usageList (17 chroms): 3 millis pass2 - checking and writing primary data (553 records, 4 fields): 5 millis CompletedMACS2peakCalling INFO @ Fri, 15 Feb 2019 08:58:05: #4 Write output xls file... ERX1236172.10_peaks.xls INFO @ Fri, 15 Feb 2019 08:58:05: #4 Write peak in narrowPeak format file... ERX1236172.10_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 08:58:05: #4 Write summits bed file... ERX1236172.10_summits.bed INFO @ Fri, 15 Feb 2019 08:58:05: Done! pass1 - making usageList (17 chroms): 3 millis pass2 - checking and writing primary data (398 records, 4 fields): 4 millis CompletedMACS2peakCalling INFO @ Fri, 15 Feb 2019 08:58:06: #4 Write output xls file... ERX1236172.20_peaks.xls INFO @ Fri, 15 Feb 2019 08:58:06: #4 Write peak in narrowPeak format file... ERX1236172.20_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 08:58:06: #4 Write summits bed file... ERX1236172.20_summits.bed INFO @ Fri, 15 Feb 2019 08:58:06: Done! pass1 - making usageList (17 chroms): 3 millis pass2 - checking and writing primary data (264 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。