Job ID = 14521834 SRX = SRX9399087 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 4034276 spots for SRR12935368/SRR12935368.sra Written 4034276 spots for SRR12935368/SRR12935368.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: 00:02:08 4034276 reads; of these: 4034276 (100.00%) were paired; of these: 577428 (14.31%) aligned concordantly 0 times 3177194 (78.75%) aligned concordantly exactly 1 time 279654 (6.93%) aligned concordantly >1 times ---- 577428 pairs aligned concordantly 0 times; of these: 95583 (16.55%) aligned discordantly 1 time ---- 481845 pairs aligned 0 times concordantly or discordantly; of these: 963690 mates make up the pairs; of these: 803110 (83.34%) aligned 0 times 131687 (13.66%) aligned exactly 1 time 28893 (3.00%) aligned >1 times 90.05% overall alignment rate Time searching: 00:02:08 Overall time: 00:02:08 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] 288994 / 3498278 = 0.0826 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 21:45:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.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 21:45:04: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:45:04: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:45:12: 1000000 INFO @ Sat, 15 Jan 2022 21:45:19: 2000000 INFO @ Sat, 15 Jan 2022 21:45:25: 3000000 INFO @ Sat, 15 Jan 2022 21:45:31: 4000000 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 21:45:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.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 21:45:34: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:45:34: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:45:37: 5000000 INFO @ Sat, 15 Jan 2022 21:45:42: 1000000 INFO @ Sat, 15 Jan 2022 21:45:44: 6000000 INFO @ Sat, 15 Jan 2022 21:45:48: #1 tag size is determined as 37 bps INFO @ Sat, 15 Jan 2022 21:45:48: #1 tag size = 37 INFO @ Sat, 15 Jan 2022 21:45:48: #1 total tags in treatment: 3169276 INFO @ Sat, 15 Jan 2022 21:45:48: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:45:48: #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 21:45:48: #1 tags after filtering in treatment: 2335216 INFO @ Sat, 15 Jan 2022 21:45:48: #1 Redundant rate of treatment: 0.26 INFO @ Sat, 15 Jan 2022 21:45:48: #1 finished! INFO @ Sat, 15 Jan 2022 21:45:48: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:45:48: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:45:48: #2 number of paired peaks: 1 WARNING @ Sat, 15 Jan 2022 21:45:48: Too few paired peaks (1) 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 21:45:48: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.05_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/SRX9399087/SRX9399087.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 21:45:50: 2000000 INFO @ Sat, 15 Jan 2022 21:45:57: 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 21:46:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.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 21:46:04: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:46:04: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:46:05: 4000000 INFO @ Sat, 15 Jan 2022 21:46:11: 1000000 INFO @ Sat, 15 Jan 2022 21:46:13: 5000000 INFO @ Sat, 15 Jan 2022 21:46:17: 2000000 INFO @ Sat, 15 Jan 2022 21:46:20: 6000000 INFO @ Sat, 15 Jan 2022 21:46:22: 3000000 INFO @ Sat, 15 Jan 2022 21:46:25: #1 tag size is determined as 37 bps INFO @ Sat, 15 Jan 2022 21:46:25: #1 tag size = 37 INFO @ Sat, 15 Jan 2022 21:46:25: #1 total tags in treatment: 3169276 INFO @ Sat, 15 Jan 2022 21:46:25: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:46:25: #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 21:46:25: #1 tags after filtering in treatment: 2335216 INFO @ Sat, 15 Jan 2022 21:46:25: #1 Redundant rate of treatment: 0.26 INFO @ Sat, 15 Jan 2022 21:46:25: #1 finished! INFO @ Sat, 15 Jan 2022 21:46:25: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:46:25: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:46:25: #2 number of paired peaks: 1 WARNING @ Sat, 15 Jan 2022 21:46:25: Too few paired peaks (1) 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 21:46:25: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.10_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/SRX9399087/SRX9399087.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 21:46:28: 4000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 21:46:33: 5000000 INFO @ Sat, 15 Jan 2022 21:46:38: 6000000 INFO @ Sat, 15 Jan 2022 21:46:42: #1 tag size is determined as 37 bps INFO @ Sat, 15 Jan 2022 21:46:42: #1 tag size = 37 INFO @ Sat, 15 Jan 2022 21:46:42: #1 total tags in treatment: 3169276 INFO @ Sat, 15 Jan 2022 21:46:42: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:46:42: #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 21:46:42: #1 tags after filtering in treatment: 2335216 INFO @ Sat, 15 Jan 2022 21:46:42: #1 Redundant rate of treatment: 0.26 INFO @ Sat, 15 Jan 2022 21:46:42: #1 finished! INFO @ Sat, 15 Jan 2022 21:46:42: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:46:42: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:46:42: #2 number of paired peaks: 1 WARNING @ Sat, 15 Jan 2022 21:46:42: Too few paired peaks (1) 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 21:46:42: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.20_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/SRX9399087/SRX9399087.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9399087/SRX9399087.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BigWig に変換しました。