Job ID = 14519681 SRX = SRX9067171 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 5605059 spots for SRR12580324/SRR12580324.sra Written 5605059 spots for SRR12580324/SRR12580324.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: 00:03:53 5605059 reads; of these: 5605059 (100.00%) were paired; of these: 1448508 (25.84%) aligned concordantly 0 times 3671356 (65.50%) aligned concordantly exactly 1 time 485195 (8.66%) aligned concordantly >1 times ---- 1448508 pairs aligned concordantly 0 times; of these: 168307 (11.62%) aligned discordantly 1 time ---- 1280201 pairs aligned 0 times concordantly or discordantly; of these: 2560402 mates make up the pairs; of these: 2356949 (92.05%) aligned 0 times 142970 (5.58%) aligned exactly 1 time 60483 (2.36%) aligned >1 times 78.97% overall alignment rate Time searching: 00:03:53 Overall time: 00:03:53 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] 504663 / 4250767 = 0.1187 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 17:28:48: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.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 17:28:48: #1 read tag files... INFO @ Sat, 15 Jan 2022 17:28:48: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 17:28:55: 1000000 INFO @ Sat, 15 Jan 2022 17:29:03: 2000000 INFO @ Sat, 15 Jan 2022 17:29:10: 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 17:29:17: 4000000 INFO @ Sat, 15 Jan 2022 17:29:18: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.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 17:29:18: #1 read tag files... INFO @ Sat, 15 Jan 2022 17:29:18: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 17:29:25: 5000000 INFO @ Sat, 15 Jan 2022 17:29:26: 1000000 INFO @ Sat, 15 Jan 2022 17:29:32: 6000000 INFO @ Sat, 15 Jan 2022 17:29:33: 2000000 INFO @ Sat, 15 Jan 2022 17:29:40: 7000000 INFO @ Sat, 15 Jan 2022 17:29:41: 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 17:29:46: #1 tag size is determined as 50 bps INFO @ Sat, 15 Jan 2022 17:29:46: #1 tag size = 50 INFO @ Sat, 15 Jan 2022 17:29:46: #1 total tags in treatment: 3659843 INFO @ Sat, 15 Jan 2022 17:29:46: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 17:29:46: #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 17:29:46: #1 tags after filtering in treatment: 2615406 INFO @ Sat, 15 Jan 2022 17:29:46: #1 Redundant rate of treatment: 0.29 INFO @ Sat, 15 Jan 2022 17:29:46: #1 finished! INFO @ Sat, 15 Jan 2022 17:29:46: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 17:29:46: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 17:29:46: #2 number of paired peaks: 10 WARNING @ Sat, 15 Jan 2022 17:29:46: Too few paired peaks (10) 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 17:29:46: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.05_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/sacCer3/SRX9067171/SRX9067171.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 17:29:48: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.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 17:29:48: #1 read tag files... INFO @ Sat, 15 Jan 2022 17:29:48: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 17:29:48: 4000000 INFO @ Sat, 15 Jan 2022 17:29:54: 1000000 INFO @ Sat, 15 Jan 2022 17:29:56: 5000000 INFO @ Sat, 15 Jan 2022 17:29:59: 2000000 INFO @ Sat, 15 Jan 2022 17:30:03: 6000000 INFO @ Sat, 15 Jan 2022 17:30:05: 3000000 INFO @ Sat, 15 Jan 2022 17:30:10: 7000000 INFO @ Sat, 15 Jan 2022 17:30:11: 4000000 INFO @ Sat, 15 Jan 2022 17:30:16: #1 tag size is determined as 50 bps INFO @ Sat, 15 Jan 2022 17:30:16: #1 tag size = 50 INFO @ Sat, 15 Jan 2022 17:30:16: #1 total tags in treatment: 3659843 INFO @ Sat, 15 Jan 2022 17:30:16: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 17:30:16: #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 17:30:16: #1 tags after filtering in treatment: 2615406 INFO @ Sat, 15 Jan 2022 17:30:16: #1 Redundant rate of treatment: 0.29 INFO @ Sat, 15 Jan 2022 17:30:16: #1 finished! INFO @ Sat, 15 Jan 2022 17:30:16: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 17:30:16: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 17:30:16: #2 number of paired peaks: 10 WARNING @ Sat, 15 Jan 2022 17:30:16: Too few paired peaks (10) 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 17:30:16: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.10_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/SRX9067171/SRX9067171.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 17:30:17: 5000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 17:30:22: 6000000 INFO @ Sat, 15 Jan 2022 17:30:28: 7000000 BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 17:30:32: #1 tag size is determined as 50 bps INFO @ Sat, 15 Jan 2022 17:30:32: #1 tag size = 50 INFO @ Sat, 15 Jan 2022 17:30:32: #1 total tags in treatment: 3659843 INFO @ Sat, 15 Jan 2022 17:30:32: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 17:30:32: #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 17:30:32: #1 tags after filtering in treatment: 2615406 INFO @ Sat, 15 Jan 2022 17:30:32: #1 Redundant rate of treatment: 0.29 INFO @ Sat, 15 Jan 2022 17:30:32: #1 finished! INFO @ Sat, 15 Jan 2022 17:30:32: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 17:30:32: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 17:30:33: #2 number of paired peaks: 10 WARNING @ Sat, 15 Jan 2022 17:30:33: Too few paired peaks (10) 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 17:30:33: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.20_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/SRX9067171/SRX9067171.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9067171/SRX9067171.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling