Job ID = 10224026 SRX = SRX8754215 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 4204316 spots for SRR12246286/SRR12246286.sra Written 4204316 spots for SRR12246286/SRR12246286.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: 00:01:53 4204316 reads; of these: 4204316 (100.00%) were paired; of these: 220679 (5.25%) aligned concordantly 0 times 3679257 (87.51%) aligned concordantly exactly 1 time 304380 (7.24%) aligned concordantly >1 times ---- 220679 pairs aligned concordantly 0 times; of these: 123460 (55.95%) aligned discordantly 1 time ---- 97219 pairs aligned 0 times concordantly or discordantly; of these: 194438 mates make up the pairs; of these: 150294 (77.30%) aligned 0 times 21802 (11.21%) aligned exactly 1 time 22342 (11.49%) aligned >1 times 98.21% overall alignment rate Time searching: 00:01:53 Overall time: 00:01:53 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] 31605 / 4101746 = 0.0077 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 @ Fri, 16 Oct 2020 09:13:51: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.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 @ Fri, 16 Oct 2020 09:13:51: #1 read tag files... INFO @ Fri, 16 Oct 2020 09:13:51: #1 read treatment tags... INFO @ Fri, 16 Oct 2020 09:13:55: 1000000 INFO @ Fri, 16 Oct 2020 09:13:59: 2000000 INFO @ Fri, 16 Oct 2020 09:14:03: 3000000 INFO @ Fri, 16 Oct 2020 09:14:08: 4000000 INFO @ Fri, 16 Oct 2020 09:14:12: 5000000 INFO @ Fri, 16 Oct 2020 09:14:16: 6000000 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 @ Fri, 16 Oct 2020 09:14:20: 7000000 INFO @ Fri, 16 Oct 2020 09:14:21: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.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 @ Fri, 16 Oct 2020 09:14:21: #1 read tag files... INFO @ Fri, 16 Oct 2020 09:14:21: #1 read treatment tags... INFO @ Fri, 16 Oct 2020 09:14:25: 8000000 INFO @ Fri, 16 Oct 2020 09:14:26: #1 tag size is determined as 38 bps INFO @ Fri, 16 Oct 2020 09:14:26: #1 tag size = 38 INFO @ Fri, 16 Oct 2020 09:14:26: #1 total tags in treatment: 3952369 INFO @ Fri, 16 Oct 2020 09:14:26: #1 user defined the maximum tags... INFO @ Fri, 16 Oct 2020 09:14:26: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 16 Oct 2020 09:14:26: #1 tags after filtering in treatment: 3511126 INFO @ Fri, 16 Oct 2020 09:14:26: #1 Redundant rate of treatment: 0.11 INFO @ Fri, 16 Oct 2020 09:14:26: #1 finished! INFO @ Fri, 16 Oct 2020 09:14:26: #2 Build Peak Model... INFO @ Fri, 16 Oct 2020 09:14:26: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 16 Oct 2020 09:14:26: 1000000 INFO @ Fri, 16 Oct 2020 09:14:26: #2 number of paired peaks: 0 WARNING @ Fri, 16 Oct 2020 09:14:26: Too few paired peaks (0) 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 @ Fri, 16 Oct 2020 09:14:26: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.05_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/SRX8754215/SRX8754215.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 16 Oct 2020 09:14:31: 2000000 INFO @ Fri, 16 Oct 2020 09:14:37: 3000000 INFO @ Fri, 16 Oct 2020 09:14:42: 4000000 INFO @ Fri, 16 Oct 2020 09:14:47: 5000000 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 @ Fri, 16 Oct 2020 09:14:51: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.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 @ Fri, 16 Oct 2020 09:14:51: #1 read tag files... INFO @ Fri, 16 Oct 2020 09:14:51: #1 read treatment tags... INFO @ Fri, 16 Oct 2020 09:14:52: 6000000 INFO @ Fri, 16 Oct 2020 09:14:56: 1000000 INFO @ Fri, 16 Oct 2020 09:14:58: 7000000 INFO @ Fri, 16 Oct 2020 09:15:01: 2000000 INFO @ Fri, 16 Oct 2020 09:15:03: 8000000 INFO @ Fri, 16 Oct 2020 09:15:04: #1 tag size is determined as 38 bps INFO @ Fri, 16 Oct 2020 09:15:04: #1 tag size = 38 INFO @ Fri, 16 Oct 2020 09:15:04: #1 total tags in treatment: 3952369 INFO @ Fri, 16 Oct 2020 09:15:04: #1 user defined the maximum tags... INFO @ Fri, 16 Oct 2020 09:15:04: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 16 Oct 2020 09:15:04: #1 tags after filtering in treatment: 3511126 INFO @ Fri, 16 Oct 2020 09:15:04: #1 Redundant rate of treatment: 0.11 INFO @ Fri, 16 Oct 2020 09:15:04: #1 finished! INFO @ Fri, 16 Oct 2020 09:15:04: #2 Build Peak Model... INFO @ Fri, 16 Oct 2020 09:15:04: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 16 Oct 2020 09:15:04: #2 number of paired peaks: 0 WARNING @ Fri, 16 Oct 2020 09:15:04: Too few paired peaks (0) 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 @ Fri, 16 Oct 2020 09:15:04: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.10_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 0 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 16 Oct 2020 09:15:05: 3000000 INFO @ Fri, 16 Oct 2020 09:15:10: 4000000 INFO @ Fri, 16 Oct 2020 09:15:15: 5000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Fri, 16 Oct 2020 09:15:19: 6000000 INFO @ Fri, 16 Oct 2020 09:15:24: 7000000 BigWig に変換しました。 INFO @ Fri, 16 Oct 2020 09:15:28: 8000000 INFO @ Fri, 16 Oct 2020 09:15:29: #1 tag size is determined as 38 bps INFO @ Fri, 16 Oct 2020 09:15:29: #1 tag size = 38 INFO @ Fri, 16 Oct 2020 09:15:29: #1 total tags in treatment: 3952369 INFO @ Fri, 16 Oct 2020 09:15:29: #1 user defined the maximum tags... INFO @ Fri, 16 Oct 2020 09:15:29: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 16 Oct 2020 09:15:29: #1 tags after filtering in treatment: 3511126 INFO @ Fri, 16 Oct 2020 09:15:29: #1 Redundant rate of treatment: 0.11 INFO @ Fri, 16 Oct 2020 09:15:29: #1 finished! INFO @ Fri, 16 Oct 2020 09:15:29: #2 Build Peak Model... INFO @ Fri, 16 Oct 2020 09:15:29: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 16 Oct 2020 09:15:29: #2 number of paired peaks: 0 WARNING @ Fri, 16 Oct 2020 09:15:29: Too few paired peaks (0) 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 @ Fri, 16 Oct 2020 09:15:29: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.20_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/SRX8754215/SRX8754215.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8754215/SRX8754215.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling