Job ID = 14521711 SRX = ERX4439621 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 4164546 spots for ERR4501550/ERR4501550.sra Written 4164546 spots for ERR4501550/ERR4501550.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: 00:03:26 4164546 reads; of these: 4164546 (100.00%) were paired; of these: 1077244 (25.87%) aligned concordantly 0 times 2739904 (65.79%) aligned concordantly exactly 1 time 347398 (8.34%) aligned concordantly >1 times ---- 1077244 pairs aligned concordantly 0 times; of these: 444627 (41.27%) aligned discordantly 1 time ---- 632617 pairs aligned 0 times concordantly or discordantly; of these: 1265234 mates make up the pairs; of these: 1084346 (85.70%) aligned 0 times 64284 (5.08%) aligned exactly 1 time 116604 (9.22%) aligned >1 times 86.98% overall alignment rate Time searching: 00:03:26 Overall time: 00:03:26 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] 59419 / 3501051 = 0.0170 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 21:37:38: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.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 21:37:38: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:37:38: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:37:43: 1000000 INFO @ Sat, 15 Jan 2022 21:37:48: 2000000 INFO @ Sat, 15 Jan 2022 21:37:53: 3000000 INFO @ Sat, 15 Jan 2022 21:37:58: 4000000 INFO @ Sat, 15 Jan 2022 21:38:03: 5000000 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 21:38:08: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.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 21:38:08: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:38:08: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:38:09: 6000000 INFO @ Sat, 15 Jan 2022 21:38:14: 7000000 INFO @ Sat, 15 Jan 2022 21:38:14: #1 tag size is determined as 100 bps INFO @ Sat, 15 Jan 2022 21:38:14: #1 tag size = 100 INFO @ Sat, 15 Jan 2022 21:38:14: #1 total tags in treatment: 3036791 INFO @ Sat, 15 Jan 2022 21:38:14: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:38:14: #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 21:38:14: #1 tags after filtering in treatment: 2687441 INFO @ Sat, 15 Jan 2022 21:38:14: #1 Redundant rate of treatment: 0.12 INFO @ Sat, 15 Jan 2022 21:38:14: #1 finished! INFO @ Sat, 15 Jan 2022 21:38:14: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:38:14: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:38:14: 1000000 INFO @ Sat, 15 Jan 2022 21:38:15: #2 number of paired peaks: 95 WARNING @ Sat, 15 Jan 2022 21:38:15: Too few paired peaks (95) 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 21:38:15: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.05_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/ERX4439621/ERX4439621.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 21:38:20: 2000000 INFO @ Sat, 15 Jan 2022 21:38:26: 3000000 INFO @ Sat, 15 Jan 2022 21:38:32: 4000000 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 21:38:38: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.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 21:38:38: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:38:38: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:38:38: 5000000 INFO @ Sat, 15 Jan 2022 21:38:45: 1000000 INFO @ Sat, 15 Jan 2022 21:38:45: 6000000 INFO @ Sat, 15 Jan 2022 21:38:51: 7000000 INFO @ Sat, 15 Jan 2022 21:38:51: 2000000 INFO @ Sat, 15 Jan 2022 21:38:52: #1 tag size is determined as 100 bps INFO @ Sat, 15 Jan 2022 21:38:52: #1 tag size = 100 INFO @ Sat, 15 Jan 2022 21:38:52: #1 total tags in treatment: 3036791 INFO @ Sat, 15 Jan 2022 21:38:52: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:38:52: #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 21:38:52: #1 tags after filtering in treatment: 2687441 INFO @ Sat, 15 Jan 2022 21:38:52: #1 Redundant rate of treatment: 0.12 INFO @ Sat, 15 Jan 2022 21:38:52: #1 finished! INFO @ Sat, 15 Jan 2022 21:38:52: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:38:52: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:38:52: #2 number of paired peaks: 95 WARNING @ Sat, 15 Jan 2022 21:38:52: Too few paired peaks (95) 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 21:38:52: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.10_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/ERX4439621/ERX4439621.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 21:38:57: 3000000 INFO @ Sat, 15 Jan 2022 21:39:03: 4000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 21:39:10: 5000000 INFO @ Sat, 15 Jan 2022 21:39:16: 6000000 BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 21:39:22: 7000000 INFO @ Sat, 15 Jan 2022 21:39:23: #1 tag size is determined as 100 bps INFO @ Sat, 15 Jan 2022 21:39:23: #1 tag size = 100 INFO @ Sat, 15 Jan 2022 21:39:23: #1 total tags in treatment: 3036791 INFO @ Sat, 15 Jan 2022 21:39:23: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:39:23: #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 21:39:23: #1 tags after filtering in treatment: 2687441 INFO @ Sat, 15 Jan 2022 21:39:23: #1 Redundant rate of treatment: 0.12 INFO @ Sat, 15 Jan 2022 21:39:23: #1 finished! INFO @ Sat, 15 Jan 2022 21:39:23: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:39:23: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:39:23: #2 number of paired peaks: 95 WARNING @ Sat, 15 Jan 2022 21:39:23: Too few paired peaks (95) 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 21:39:23: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.20_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/ERX4439621/ERX4439621.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439621/ERX4439621.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling