Job ID = 12264915 SRX = SRX3088366 Genome = dm3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 11556 spots for SRR5928044/SRR5928044.sra Written 11556 spots for SRR5928044/SRR5928044.sra fastq に変換しました。 bowtie でマッピング中... Your job 12265035 ("srTdm6") has been submitted Time loading reference: 00:00:00 Time loading forward index: 00:00:00 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:00:00 11556 reads; of these: 11556 (100.00%) were unpaired; of these: 4849 (41.96%) aligned 0 times 5217 (45.15%) aligned exactly 1 time 1490 (12.89%) aligned >1 times 58.04% overall alignment rate Time searching: 00:00:00 Overall time: 00:00:00 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 15 sequences. [bam_rmdupse_core] 1678 / 6707 = 0.2502 in library ' ' BAM に変換しました。 Bed ファイルを作成中... WARNING: Skipping mount /opt/pkg/singularity/3.7.1/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 03 Apr 2021 05:57:59: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 03 Apr 2021 05:57:59: #1 read tag files... INFO @ Sat, 03 Apr 2021 05:57:59: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 05:57:59: #1 tag size is determined as 74 bps INFO @ Sat, 03 Apr 2021 05:57:59: #1 tag size = 74 INFO @ Sat, 03 Apr 2021 05:57:59: #1 total tags in treatment: 5029 INFO @ Sat, 03 Apr 2021 05:57:59: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 05:57:59: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 03 Apr 2021 05:57:59: #1 tags after filtering in treatment: 5028 INFO @ Sat, 03 Apr 2021 05:57:59: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 03 Apr 2021 05:57:59: #1 finished! INFO @ Sat, 03 Apr 2021 05:57:59: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 05:57:59: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 05:57:59: #2 number of paired peaks: 156 WARNING @ Sat, 03 Apr 2021 05:57:59: Fewer paired peaks (156) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 156 pairs to build model! INFO @ Sat, 03 Apr 2021 05:57:59: start model_add_line... INFO @ Sat, 03 Apr 2021 05:57:59: start X-correlation... INFO @ Sat, 03 Apr 2021 05:57:59: end of X-cor INFO @ Sat, 03 Apr 2021 05:57:59: #2 finished! INFO @ Sat, 03 Apr 2021 05:57:59: #2 predicted fragment length is 176 bps INFO @ Sat, 03 Apr 2021 05:57:59: #2 alternative fragment length(s) may be 8,58,81,122,145,176,190,217,249,283,301,352,412,507,542 bps INFO @ Sat, 03 Apr 2021 05:57:59: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.05_model.r INFO @ Sat, 03 Apr 2021 05:57:59: #3 Call peaks... INFO @ Sat, 03 Apr 2021 05:57:59: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 05:57:59: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 05:57:59: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.05_peaks.xls INFO @ Sat, 03 Apr 2021 05:57:59: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.05_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 05:57:59: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.05_summits.bed INFO @ Sat, 03 Apr 2021 05:57:59: Done! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling WARNING: Skipping mount /opt/pkg/singularity/3.7.1/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 03 Apr 2021 05:58:29: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 03 Apr 2021 05:58:29: #1 read tag files... INFO @ Sat, 03 Apr 2021 05:58:29: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 05:58:29: #1 tag size is determined as 74 bps INFO @ Sat, 03 Apr 2021 05:58:29: #1 tag size = 74 INFO @ Sat, 03 Apr 2021 05:58:29: #1 total tags in treatment: 5029 INFO @ Sat, 03 Apr 2021 05:58:29: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 05:58:29: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 03 Apr 2021 05:58:29: #1 tags after filtering in treatment: 5028 INFO @ Sat, 03 Apr 2021 05:58:29: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 03 Apr 2021 05:58:29: #1 finished! INFO @ Sat, 03 Apr 2021 05:58:29: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 05:58:29: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 05:58:29: #2 number of paired peaks: 156 WARNING @ Sat, 03 Apr 2021 05:58:29: Fewer paired peaks (156) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 156 pairs to build model! INFO @ Sat, 03 Apr 2021 05:58:29: start model_add_line... INFO @ Sat, 03 Apr 2021 05:58:29: start X-correlation... INFO @ Sat, 03 Apr 2021 05:58:29: end of X-cor INFO @ Sat, 03 Apr 2021 05:58:29: #2 finished! INFO @ Sat, 03 Apr 2021 05:58:29: #2 predicted fragment length is 176 bps INFO @ Sat, 03 Apr 2021 05:58:29: #2 alternative fragment length(s) may be 8,58,81,122,145,176,190,217,249,283,301,352,412,507,542 bps INFO @ Sat, 03 Apr 2021 05:58:29: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.10_model.r INFO @ Sat, 03 Apr 2021 05:58:29: #3 Call peaks... INFO @ Sat, 03 Apr 2021 05:58:29: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 05:58:29: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 05:58:29: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.10_peaks.xls INFO @ Sat, 03 Apr 2021 05:58:29: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.10_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 05:58:29: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.10_summits.bed INFO @ Sat, 03 Apr 2021 05:58:29: Done! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.7.1/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 INFO @ Sat, 03 Apr 2021 05:58:59: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 03 Apr 2021 05:58:59: #1 read tag files... INFO @ Sat, 03 Apr 2021 05:58:59: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 05:58:59: #1 tag size is determined as 74 bps INFO @ Sat, 03 Apr 2021 05:58:59: #1 tag size = 74 INFO @ Sat, 03 Apr 2021 05:58:59: #1 total tags in treatment: 5029 INFO @ Sat, 03 Apr 2021 05:58:59: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 05:58:59: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 03 Apr 2021 05:58:59: #1 tags after filtering in treatment: 5028 INFO @ Sat, 03 Apr 2021 05:58:59: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 03 Apr 2021 05:58:59: #1 finished! INFO @ Sat, 03 Apr 2021 05:58:59: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 05:58:59: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 05:58:59: #2 number of paired peaks: 156 WARNING @ Sat, 03 Apr 2021 05:58:59: Fewer paired peaks (156) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 156 pairs to build model! INFO @ Sat, 03 Apr 2021 05:58:59: start model_add_line... INFO @ Sat, 03 Apr 2021 05:58:59: start X-correlation... INFO @ Sat, 03 Apr 2021 05:58:59: end of X-cor INFO @ Sat, 03 Apr 2021 05:58:59: #2 finished! INFO @ Sat, 03 Apr 2021 05:58:59: #2 predicted fragment length is 176 bps INFO @ Sat, 03 Apr 2021 05:58:59: #2 alternative fragment length(s) may be 8,58,81,122,145,176,190,217,249,283,301,352,412,507,542 bps INFO @ Sat, 03 Apr 2021 05:58:59: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.20_model.r INFO @ Sat, 03 Apr 2021 05:58:59: #3 Call peaks... INFO @ Sat, 03 Apr 2021 05:58:59: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 05:58:59: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 05:58:59: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.20_peaks.xls INFO @ Sat, 03 Apr 2021 05:58:59: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.20_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 05:58:59: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX3088366/SRX3088366.20_summits.bed INFO @ Sat, 03 Apr 2021 05:58:59: Done! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling