Job ID = 14521645 SRX = SRX9399137 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 7438703 spots for SRR12935418/SRR12935418.sra Written 7438703 spots for SRR12935418/SRR12935418.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: 00:03:06 7438703 reads; of these: 7438703 (100.00%) were paired; of these: 1389861 (18.68%) aligned concordantly 0 times 5498599 (73.92%) aligned concordantly exactly 1 time 550243 (7.40%) aligned concordantly >1 times ---- 1389861 pairs aligned concordantly 0 times; of these: 155982 (11.22%) aligned discordantly 1 time ---- 1233879 pairs aligned 0 times concordantly or discordantly; of these: 2467758 mates make up the pairs; of these: 2137553 (86.62%) aligned 0 times 259708 (10.52%) aligned exactly 1 time 70497 (2.86%) aligned >1 times 85.63% overall alignment rate Time searching: 00:03:06 Overall time: 00:03:06 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_sort_core] merging from 8 files... [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] 925138 / 6191549 = 0.1494 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 21:26:18: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.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 21:26:18: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:26:18: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:26:22: 1000000 INFO @ Sat, 15 Jan 2022 21:26:26: 2000000 INFO @ Sat, 15 Jan 2022 21:26:30: 3000000 INFO @ Sat, 15 Jan 2022 21:26:35: 4000000 INFO @ Sat, 15 Jan 2022 21:26:38: 5000000 INFO @ Sat, 15 Jan 2022 21:26:42: 6000000 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 21:26:46: 7000000 INFO @ Sat, 15 Jan 2022 21:26:48: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.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 21:26:48: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:26:48: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:26:50: 8000000 INFO @ Sat, 15 Jan 2022 21:26:52: 1000000 INFO @ Sat, 15 Jan 2022 21:26:54: 9000000 INFO @ Sat, 15 Jan 2022 21:26:56: 2000000 INFO @ Sat, 15 Jan 2022 21:26:58: 10000000 INFO @ Sat, 15 Jan 2022 21:27:00: 3000000 INFO @ Sat, 15 Jan 2022 21:27:01: #1 tag size is determined as 37 bps INFO @ Sat, 15 Jan 2022 21:27:01: #1 tag size = 37 INFO @ Sat, 15 Jan 2022 21:27:01: #1 total tags in treatment: 5136213 INFO @ Sat, 15 Jan 2022 21:27:01: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:27:01: #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 21:27:01: #1 tags after filtering in treatment: 3460099 INFO @ Sat, 15 Jan 2022 21:27:01: #1 Redundant rate of treatment: 0.33 INFO @ Sat, 15 Jan 2022 21:27:01: #1 finished! INFO @ Sat, 15 Jan 2022 21:27:01: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:27:01: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:27:02: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 21:27:02: 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 @ Sat, 15 Jan 2022 21:27:02: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.05_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/SRX9399137/SRX9399137.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 21:27:04: 4000000 INFO @ Sat, 15 Jan 2022 21:27:08: 5000000 INFO @ Sat, 15 Jan 2022 21:27:13: 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 21:27:17: 7000000 INFO @ Sat, 15 Jan 2022 21:27:18: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.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 21:27:18: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:27:18: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:27:21: 8000000 INFO @ Sat, 15 Jan 2022 21:27:22: 1000000 INFO @ Sat, 15 Jan 2022 21:27:26: 9000000 INFO @ Sat, 15 Jan 2022 21:27:26: 2000000 INFO @ Sat, 15 Jan 2022 21:27:30: 10000000 INFO @ Sat, 15 Jan 2022 21:27:31: 3000000 INFO @ Sat, 15 Jan 2022 21:27:34: #1 tag size is determined as 37 bps INFO @ Sat, 15 Jan 2022 21:27:34: #1 tag size = 37 INFO @ Sat, 15 Jan 2022 21:27:34: #1 total tags in treatment: 5136213 INFO @ Sat, 15 Jan 2022 21:27:34: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:27:34: #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 21:27:35: #1 tags after filtering in treatment: 3460099 INFO @ Sat, 15 Jan 2022 21:27:35: #1 Redundant rate of treatment: 0.33 INFO @ Sat, 15 Jan 2022 21:27:35: #1 finished! INFO @ Sat, 15 Jan 2022 21:27:35: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:27:35: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:27:35: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 21:27:35: 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 @ Sat, 15 Jan 2022 21:27:35: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.10_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/SRX9399137/SRX9399137.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 21:27:35: 4000000 INFO @ Sat, 15 Jan 2022 21:27:39: 5000000 INFO @ Sat, 15 Jan 2022 21:27:43: 6000000 INFO @ Sat, 15 Jan 2022 21:27:47: 7000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 21:27:51: 8000000 INFO @ Sat, 15 Jan 2022 21:27:55: 9000000 INFO @ Sat, 15 Jan 2022 21:27:58: 10000000 BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 21:28:02: #1 tag size is determined as 37 bps INFO @ Sat, 15 Jan 2022 21:28:02: #1 tag size = 37 INFO @ Sat, 15 Jan 2022 21:28:02: #1 total tags in treatment: 5136213 INFO @ Sat, 15 Jan 2022 21:28:02: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:28:02: #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 21:28:02: #1 tags after filtering in treatment: 3460099 INFO @ Sat, 15 Jan 2022 21:28:02: #1 Redundant rate of treatment: 0.33 INFO @ Sat, 15 Jan 2022 21:28:02: #1 finished! INFO @ Sat, 15 Jan 2022 21:28:02: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:28:02: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:28:02: #2 number of paired peaks: 0 WARNING @ Sat, 15 Jan 2022 21:28:02: 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 @ Sat, 15 Jan 2022 21:28:02: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.20_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/SRX9399137/SRX9399137.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9399137/SRX9399137.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling