Job ID = 14521887 SRX = ERX4439571 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 3774219 spots for ERR4501500/ERR4501500.sra Written 3774219 spots for ERR4501500/ERR4501500.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: 00:02:53 3774219 reads; of these: 3774219 (100.00%) were paired; of these: 1197134 (31.72%) aligned concordantly 0 times 2131961 (56.49%) aligned concordantly exactly 1 time 445124 (11.79%) aligned concordantly >1 times ---- 1197134 pairs aligned concordantly 0 times; of these: 555588 (46.41%) aligned discordantly 1 time ---- 641546 pairs aligned 0 times concordantly or discordantly; of these: 1283092 mates make up the pairs; of these: 960974 (74.90%) aligned 0 times 74756 (5.83%) aligned exactly 1 time 247362 (19.28%) aligned >1 times 87.27% overall alignment rate Time searching: 00:02:53 Overall time: 00:02:53 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] 57340 / 3094361 = 0.0185 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 21:54:58: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.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 21:54:58: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:54:58: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:55:07: 1000000 INFO @ Sat, 15 Jan 2022 21:55:16: 2000000 INFO @ Sat, 15 Jan 2022 21:55:24: 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 21:55:28: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.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 21:55:28: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:55:28: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:55:34: 4000000 INFO @ Sat, 15 Jan 2022 21:55:37: 1000000 INFO @ Sat, 15 Jan 2022 21:55:44: 5000000 INFO @ Sat, 15 Jan 2022 21:55:47: 2000000 INFO @ Sat, 15 Jan 2022 21:55:54: 6000000 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 21:55:57: 3000000 INFO @ Sat, 15 Jan 2022 21:55:58: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.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 21:55:58: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:55:58: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:55:58: #1 tag size is determined as 100 bps INFO @ Sat, 15 Jan 2022 21:55:58: #1 tag size = 100 INFO @ Sat, 15 Jan 2022 21:55:58: #1 total tags in treatment: 2529181 INFO @ Sat, 15 Jan 2022 21:55:58: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:55:58: #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 21:55:58: #1 tags after filtering in treatment: 2172089 INFO @ Sat, 15 Jan 2022 21:55:58: #1 Redundant rate of treatment: 0.14 INFO @ Sat, 15 Jan 2022 21:55:58: #1 finished! INFO @ Sat, 15 Jan 2022 21:55:58: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:55:58: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:55:59: #2 number of paired peaks: 39 WARNING @ Sat, 15 Jan 2022 21:55:59: Too few paired peaks (39) 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 21:55:59: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.05_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/ERX4439571/ERX4439571.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 21:56:06: 4000000 INFO @ Sat, 15 Jan 2022 21:56:07: 1000000 INFO @ Sat, 15 Jan 2022 21:56:16: 2000000 INFO @ Sat, 15 Jan 2022 21:56:16: 5000000 INFO @ Sat, 15 Jan 2022 21:56:25: 3000000 INFO @ Sat, 15 Jan 2022 21:56:26: 6000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 21:56:30: #1 tag size is determined as 100 bps INFO @ Sat, 15 Jan 2022 21:56:30: #1 tag size = 100 INFO @ Sat, 15 Jan 2022 21:56:30: #1 total tags in treatment: 2529181 INFO @ Sat, 15 Jan 2022 21:56:30: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:56:30: #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 21:56:30: #1 tags after filtering in treatment: 2172089 INFO @ Sat, 15 Jan 2022 21:56:30: #1 Redundant rate of treatment: 0.14 INFO @ Sat, 15 Jan 2022 21:56:30: #1 finished! INFO @ Sat, 15 Jan 2022 21:56:30: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:56:30: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:56:30: #2 number of paired peaks: 39 WARNING @ Sat, 15 Jan 2022 21:56:30: Too few paired peaks (39) 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 21:56:30: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.10_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/ERX4439571/ERX4439571.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 21:56:33: 4000000 BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 21:56:41: 5000000 INFO @ Sat, 15 Jan 2022 21:56:48: 6000000 INFO @ Sat, 15 Jan 2022 21:56:51: #1 tag size is determined as 100 bps INFO @ Sat, 15 Jan 2022 21:56:51: #1 tag size = 100 INFO @ Sat, 15 Jan 2022 21:56:51: #1 total tags in treatment: 2529181 INFO @ Sat, 15 Jan 2022 21:56:51: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:56:51: #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 21:56:51: #1 tags after filtering in treatment: 2172089 INFO @ Sat, 15 Jan 2022 21:56:51: #1 Redundant rate of treatment: 0.14 INFO @ Sat, 15 Jan 2022 21:56:51: #1 finished! INFO @ Sat, 15 Jan 2022 21:56:51: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:56:51: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:56:52: #2 number of paired peaks: 39 WARNING @ Sat, 15 Jan 2022 21:56:52: Too few paired peaks (39) 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 21:56:52: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.20_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/ERX4439571/ERX4439571.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439571/ERX4439571.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling