Job ID = 14522074 SRX = SRX9067225 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 4486823 spots for SRR12580378/SRR12580378.sra Written 4486823 spots for SRR12580378/SRR12580378.sra 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: 00:03:23 4486823 reads; of these: 4486823 (100.00%) were paired; of these: 968887 (21.59%) aligned concordantly 0 times 3011807 (67.13%) aligned concordantly exactly 1 time 506129 (11.28%) aligned concordantly >1 times ---- 968887 pairs aligned concordantly 0 times; of these: 166500 (17.18%) aligned discordantly 1 time ---- 802387 pairs aligned 0 times concordantly or discordantly; of these: 1604774 mates make up the pairs; of these: 1404418 (87.52%) aligned 0 times 128303 (8.00%) aligned exactly 1 time 72053 (4.49%) aligned >1 times 84.35% overall alignment rate Time searching: 00:03:23 Overall time: 00:03:23 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] 600372 / 3613231 = 0.1662 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/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 22:12:47: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.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 Jan 2022 22:12:47: #1 read tag files... INFO @ Sat, 15 Jan 2022 22:12:47: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 22:12:54: 1000000 INFO @ Sat, 15 Jan 2022 22:13:01: 2000000 INFO @ Sat, 15 Jan 2022 22:13:09: 3000000 WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 22:13:16: 4000000 INFO @ Sat, 15 Jan 2022 22:13:17: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.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 Jan 2022 22:13:17: #1 read tag files... INFO @ Sat, 15 Jan 2022 22:13:17: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 22:13:23: 5000000 INFO @ Sat, 15 Jan 2022 22:13:25: 1000000 INFO @ Sat, 15 Jan 2022 22:13:31: 6000000 INFO @ Sat, 15 Jan 2022 22:13:33: #1 tag size is determined as 51 bps INFO @ Sat, 15 Jan 2022 22:13:33: #1 tag size = 51 INFO @ Sat, 15 Jan 2022 22:13:33: #1 total tags in treatment: 2927086 INFO @ Sat, 15 Jan 2022 22:13:33: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 22:13:33: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 22:13:33: #1 tags after filtering in treatment: 2168511 INFO @ Sat, 15 Jan 2022 22:13:33: #1 Redundant rate of treatment: 0.26 INFO @ Sat, 15 Jan 2022 22:13:33: #1 finished! INFO @ Sat, 15 Jan 2022 22:13:33: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 22:13:33: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 22:13:33: #2 number of paired peaks: 29 WARNING @ Sat, 15 Jan 2022 22:13:33: Too few paired peaks (29) 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, 15 Jan 2022 22:13:33: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.05_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 22:13:35: 2000000 INFO @ Sat, 15 Jan 2022 22:13:42: 3000000 BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 22:13:47: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.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 Jan 2022 22:13:47: #1 read tag files... INFO @ Sat, 15 Jan 2022 22:13:47: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 22:13:50: 4000000 INFO @ Sat, 15 Jan 2022 22:13:55: 1000000 INFO @ Sat, 15 Jan 2022 22:13:59: 5000000 INFO @ Sat, 15 Jan 2022 22:14:02: 2000000 INFO @ Sat, 15 Jan 2022 22:14:06: 6000000 INFO @ Sat, 15 Jan 2022 22:14:09: #1 tag size is determined as 51 bps INFO @ Sat, 15 Jan 2022 22:14:09: #1 tag size = 51 INFO @ Sat, 15 Jan 2022 22:14:09: #1 total tags in treatment: 2927086 INFO @ Sat, 15 Jan 2022 22:14:09: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 22:14:09: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 22:14:09: #1 tags after filtering in treatment: 2168511 INFO @ Sat, 15 Jan 2022 22:14:09: #1 Redundant rate of treatment: 0.26 INFO @ Sat, 15 Jan 2022 22:14:09: #1 finished! INFO @ Sat, 15 Jan 2022 22:14:09: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 22:14:09: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 22:14:09: #2 number of paired peaks: 29 WARNING @ Sat, 15 Jan 2022 22:14:09: Too few paired peaks (29) 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, 15 Jan 2022 22:14:09: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.10_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/sacCer3/SRX9067225/SRX9067225.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 22:14:10: 3000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 22:14:17: 4000000 BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 22:14:25: 5000000 INFO @ Sat, 15 Jan 2022 22:14:33: 6000000 INFO @ Sat, 15 Jan 2022 22:14:36: #1 tag size is determined as 51 bps INFO @ Sat, 15 Jan 2022 22:14:36: #1 tag size = 51 INFO @ Sat, 15 Jan 2022 22:14:36: #1 total tags in treatment: 2927086 INFO @ Sat, 15 Jan 2022 22:14:36: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 22:14:36: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 22:14:36: #1 tags after filtering in treatment: 2168511 INFO @ Sat, 15 Jan 2022 22:14:36: #1 Redundant rate of treatment: 0.26 INFO @ Sat, 15 Jan 2022 22:14:36: #1 finished! INFO @ Sat, 15 Jan 2022 22:14:36: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 22:14:36: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 22:14:36: #2 number of paired peaks: 29 WARNING @ Sat, 15 Jan 2022 22:14:36: Too few paired peaks (29) 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, 15 Jan 2022 22:14:36: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.20_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/sacCer3/SRX9067225/SRX9067225.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067225/SRX9067225.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling