Job ID = 8069601 SRX = SRX7917395 Genome = dm3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2020-08-08T03:39:19 prefetch.2.10.7: 1) Downloading 'SRR11312942'... 2020-08-08T03:39:19 prefetch.2.10.7: Downloading via HTTPS... 2020-08-08T03:39:55 prefetch.2.10.7: HTTPS download succeed 2020-08-08T03:39:55 prefetch.2.10.7: 'SRR11312942' is valid 2020-08-08T03:39:55 prefetch.2.10.7: 1) 'SRR11312942' was downloaded successfully Read 2753470 spots for SRR11312942/SRR11312942.sra Written 2753470 spots for SRR11312942/SRR11312942.sra fastq に変換しました。 bowtie でマッピング中... Your job 8070165 ("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: 00:05:10 2753470 reads; of these: 2753470 (100.00%) were paired; of these: 521862 (18.95%) aligned concordantly 0 times 1704778 (61.91%) aligned concordantly exactly 1 time 526830 (19.13%) aligned concordantly >1 times ---- 521862 pairs aligned concordantly 0 times; of these: 160380 (30.73%) aligned discordantly 1 time ---- 361482 pairs aligned 0 times concordantly or discordantly; of these: 722964 mates make up the pairs; of these: 478043 (66.12%) aligned 0 times 118981 (16.46%) aligned exactly 1 time 125940 (17.42%) aligned >1 times 91.32% overall alignment rate Time searching: 00:05:10 Overall time: 00:05:10 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_rmdup_core] processing reference chr2L... [bam_rmdup_core] processing reference chr2LHet... [bam_rmdup_core] processing reference chr2R... [bam_rmdup_core] processing reference chr2RHet... [bam_rmdup_core] processing reference chr3L... [bam_rmdup_core] processing reference chr3LHet... [bam_rmdup_core] processing reference chr3R... [bam_rmdup_core] processing reference chr3RHet... [bam_rmdup_core] processing reference chr4... [bam_rmdup_core] processing reference chrM... [bam_rmdup_core] processing reference chrU... [bam_rmdup_core] processing reference chrUextra... [bam_rmdup_core] processing reference chrX... [bam_rmdup_core] processing reference chrXHet... [bam_rmdup_core] processing reference chrYHet... [bam_rmdup_core] 745018 / 2381503 = 0.3128 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/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 08 Aug 2020 12:46:50: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.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, 08 Aug 2020 12:46:50: #1 read tag files... INFO @ Sat, 08 Aug 2020 12:46:50: #1 read treatment tags... INFO @ Sat, 08 Aug 2020 12:46:57: 1000000 INFO @ Sat, 08 Aug 2020 12:47:04: 2000000 INFO @ Sat, 08 Aug 2020 12:47:10: 3000000 INFO @ Sat, 08 Aug 2020 12:47:14: #1 tag size is determined as 62 bps INFO @ Sat, 08 Aug 2020 12:47:14: #1 tag size = 62 INFO @ Sat, 08 Aug 2020 12:47:14: #1 total tags in treatment: 1498167 INFO @ Sat, 08 Aug 2020 12:47:14: #1 user defined the maximum tags... INFO @ Sat, 08 Aug 2020 12:47:14: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 08 Aug 2020 12:47:14: #1 tags after filtering in treatment: 1193015 INFO @ Sat, 08 Aug 2020 12:47:14: #1 Redundant rate of treatment: 0.20 INFO @ Sat, 08 Aug 2020 12:47:14: #1 finished! INFO @ Sat, 08 Aug 2020 12:47:14: #2 Build Peak Model... INFO @ Sat, 08 Aug 2020 12:47:14: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 08 Aug 2020 12:47:14: #2 number of paired peaks: 9 WARNING @ Sat, 08 Aug 2020 12:47:14: Too few paired peaks (9) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead. WARNING @ Sat, 08 Aug 2020 12:47:14: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.05_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 08 Aug 2020 12:47:20: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.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, 08 Aug 2020 12:47:20: #1 read tag files... INFO @ Sat, 08 Aug 2020 12:47:20: #1 read treatment tags... INFO @ Sat, 08 Aug 2020 12:47:27: 1000000 INFO @ Sat, 08 Aug 2020 12:47:34: 2000000 INFO @ Sat, 08 Aug 2020 12:47:42: 3000000 INFO @ Sat, 08 Aug 2020 12:47:45: #1 tag size is determined as 62 bps INFO @ Sat, 08 Aug 2020 12:47:45: #1 tag size = 62 INFO @ Sat, 08 Aug 2020 12:47:45: #1 total tags in treatment: 1498167 INFO @ Sat, 08 Aug 2020 12:47:45: #1 user defined the maximum tags... INFO @ Sat, 08 Aug 2020 12:47:45: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 08 Aug 2020 12:47:45: #1 tags after filtering in treatment: 1193015 INFO @ Sat, 08 Aug 2020 12:47:45: #1 Redundant rate of treatment: 0.20 INFO @ Sat, 08 Aug 2020 12:47:45: #1 finished! INFO @ Sat, 08 Aug 2020 12:47:45: #2 Build Peak Model... INFO @ Sat, 08 Aug 2020 12:47:45: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 08 Aug 2020 12:47:46: #2 number of paired peaks: 9 WARNING @ Sat, 08 Aug 2020 12:47:46: Too few paired peaks (9) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead. WARNING @ Sat, 08 Aug 2020 12:47:46: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.10_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 08 Aug 2020 12:47:50: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.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, 08 Aug 2020 12:47:50: #1 read tag files... INFO @ Sat, 08 Aug 2020 12:47:50: #1 read treatment tags... INFO @ Sat, 08 Aug 2020 12:47:57: 1000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 08 Aug 2020 12:48:03: 2000000 BigWig に変換しました。 INFO @ Sat, 08 Aug 2020 12:48:09: 3000000 INFO @ Sat, 08 Aug 2020 12:48:12: #1 tag size is determined as 62 bps INFO @ Sat, 08 Aug 2020 12:48:12: #1 tag size = 62 INFO @ Sat, 08 Aug 2020 12:48:12: #1 total tags in treatment: 1498167 INFO @ Sat, 08 Aug 2020 12:48:12: #1 user defined the maximum tags... INFO @ Sat, 08 Aug 2020 12:48:12: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 08 Aug 2020 12:48:12: #1 tags after filtering in treatment: 1193015 INFO @ Sat, 08 Aug 2020 12:48:12: #1 Redundant rate of treatment: 0.20 INFO @ Sat, 08 Aug 2020 12:48:12: #1 finished! INFO @ Sat, 08 Aug 2020 12:48:12: #2 Build Peak Model... INFO @ Sat, 08 Aug 2020 12:48:12: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 08 Aug 2020 12:48:12: #2 number of paired peaks: 9 WARNING @ Sat, 08 Aug 2020 12:48:12: Too few paired peaks (9) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead. WARNING @ Sat, 08 Aug 2020 12:48:12: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.20_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX7917395/SRX7917395.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling