Job ID = 10224037 SRX = SRX8926522 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 5988275 spots for SRR12430729/SRR12430729.sra Written 5988275 spots for SRR12430729/SRR12430729.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: 00:02:40 5988275 reads; of these: 5988275 (100.00%) were paired; of these: 1672616 (27.93%) aligned concordantly 0 times 3472949 (58.00%) aligned concordantly exactly 1 time 842710 (14.07%) aligned concordantly >1 times ---- 1672616 pairs aligned concordantly 0 times; of these: 38598 (2.31%) aligned discordantly 1 time ---- 1634018 pairs aligned 0 times concordantly or discordantly; of these: 3268036 mates make up the pairs; of these: 3196136 (97.80%) aligned 0 times 35576 (1.09%) aligned exactly 1 time 36324 (1.11%) aligned >1 times 73.31% overall alignment rate Time searching: 00:02:40 Overall time: 00:02:40 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] 623554 / 4353399 = 0.1432 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 09:15:52: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.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 09:15:52: #1 read tag files... INFO @ Fri, 16 Oct 2020 09:15:52: #1 read treatment tags... INFO @ Fri, 16 Oct 2020 09:15:58: 1000000 INFO @ Fri, 16 Oct 2020 09:16:03: 2000000 INFO @ Fri, 16 Oct 2020 09:16:09: 3000000 INFO @ Fri, 16 Oct 2020 09:16:14: 4000000 INFO @ Fri, 16 Oct 2020 09:16:20: 5000000 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 09:16:22: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.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 09:16:22: #1 read tag files... INFO @ Fri, 16 Oct 2020 09:16:22: #1 read treatment tags... INFO @ Fri, 16 Oct 2020 09:16:25: 6000000 INFO @ Fri, 16 Oct 2020 09:16:27: 1000000 INFO @ Fri, 16 Oct 2020 09:16:32: 7000000 INFO @ Fri, 16 Oct 2020 09:16:32: 2000000 INFO @ Fri, 16 Oct 2020 09:16:35: #1 tag size is determined as 51 bps INFO @ Fri, 16 Oct 2020 09:16:35: #1 tag size = 51 INFO @ Fri, 16 Oct 2020 09:16:35: #1 total tags in treatment: 3693379 INFO @ Fri, 16 Oct 2020 09:16:35: #1 user defined the maximum tags... INFO @ Fri, 16 Oct 2020 09:16:35: #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 09:16:35: #1 tags after filtering in treatment: 2858317 INFO @ Fri, 16 Oct 2020 09:16:35: #1 Redundant rate of treatment: 0.23 INFO @ Fri, 16 Oct 2020 09:16:35: #1 finished! INFO @ Fri, 16 Oct 2020 09:16:35: #2 Build Peak Model... INFO @ Fri, 16 Oct 2020 09:16:35: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 16 Oct 2020 09:16:35: #2 number of paired peaks: 63 WARNING @ Fri, 16 Oct 2020 09:16:35: Too few paired peaks (63) 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 09:16:35: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.05_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/SRX8926522/SRX8926522.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 16 Oct 2020 09:16:37: 3000000 INFO @ Fri, 16 Oct 2020 09:16:42: 4000000 INFO @ Fri, 16 Oct 2020 09:16:47: 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 09:16:52: 6000000 INFO @ Fri, 16 Oct 2020 09:16:52: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.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 09:16:52: #1 read tag files... INFO @ Fri, 16 Oct 2020 09:16:52: #1 read treatment tags... INFO @ Fri, 16 Oct 2020 09:16:57: 7000000 INFO @ Fri, 16 Oct 2020 09:16:57: 1000000 INFO @ Fri, 16 Oct 2020 09:16:59: #1 tag size is determined as 51 bps INFO @ Fri, 16 Oct 2020 09:16:59: #1 tag size = 51 INFO @ Fri, 16 Oct 2020 09:16:59: #1 total tags in treatment: 3693379 INFO @ Fri, 16 Oct 2020 09:16:59: #1 user defined the maximum tags... INFO @ Fri, 16 Oct 2020 09:16:59: #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 09:16:59: #1 tags after filtering in treatment: 2858317 INFO @ Fri, 16 Oct 2020 09:16:59: #1 Redundant rate of treatment: 0.23 INFO @ Fri, 16 Oct 2020 09:16:59: #1 finished! INFO @ Fri, 16 Oct 2020 09:16:59: #2 Build Peak Model... INFO @ Fri, 16 Oct 2020 09:16:59: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 16 Oct 2020 09:16:59: #2 number of paired peaks: 63 WARNING @ Fri, 16 Oct 2020 09:16:59: Too few paired peaks (63) 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 09:16:59: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.10_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/SRX8926522/SRX8926522.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 16 Oct 2020 09:17:02: 2000000 INFO @ Fri, 16 Oct 2020 09:17:06: 3000000 INFO @ Fri, 16 Oct 2020 09:17:11: 4000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Fri, 16 Oct 2020 09:17:15: 5000000 INFO @ Fri, 16 Oct 2020 09:17:20: 6000000 BigWig に変換しました。 INFO @ Fri, 16 Oct 2020 09:17:25: 7000000 INFO @ Fri, 16 Oct 2020 09:17:27: #1 tag size is determined as 51 bps INFO @ Fri, 16 Oct 2020 09:17:27: #1 tag size = 51 INFO @ Fri, 16 Oct 2020 09:17:27: #1 total tags in treatment: 3693379 INFO @ Fri, 16 Oct 2020 09:17:27: #1 user defined the maximum tags... INFO @ Fri, 16 Oct 2020 09:17:27: #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 09:17:28: #1 tags after filtering in treatment: 2858317 INFO @ Fri, 16 Oct 2020 09:17:28: #1 Redundant rate of treatment: 0.23 INFO @ Fri, 16 Oct 2020 09:17:28: #1 finished! INFO @ Fri, 16 Oct 2020 09:17:28: #2 Build Peak Model... INFO @ Fri, 16 Oct 2020 09:17:28: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 16 Oct 2020 09:17:28: #2 number of paired peaks: 63 WARNING @ Fri, 16 Oct 2020 09:17:28: Too few paired peaks (63) 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 09:17:28: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.20_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/SRX8926522/SRX8926522.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8926522/SRX8926522.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling