Job ID = 7113694 SRX = SRX8462181 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2020-07-22T05:45:37 prefetch.2.10.7: 1) Downloading 'SRR11915640'... 2020-07-22T05:45:37 prefetch.2.10.7: Downloading via HTTPS... 2020-07-22T05:46:43 prefetch.2.10.7: HTTPS download succeed 2020-07-22T05:46:44 prefetch.2.10.7: 'SRR11915640' is valid 2020-07-22T05:46:44 prefetch.2.10.7: 1) 'SRR11915640' was downloaded successfully 2020-07-22T05:46:44 prefetch.2.10.7: 'SRR11915640' has 0 unresolved dependencies Read 5782949 spots for SRR11915640/SRR11915640.sra Written 5782949 spots for SRR11915640/SRR11915640.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: 00:05:24 5782949 reads; of these: 5782949 (100.00%) were paired; of these: 818873 (14.16%) aligned concordantly 0 times 4149105 (71.75%) aligned concordantly exactly 1 time 814971 (14.09%) aligned concordantly >1 times ---- 818873 pairs aligned concordantly 0 times; of these: 58243 (7.11%) aligned discordantly 1 time ---- 760630 pairs aligned 0 times concordantly or discordantly; of these: 1521260 mates make up the pairs; of these: 1388941 (91.30%) aligned 0 times 90261 (5.93%) aligned exactly 1 time 42058 (2.76%) aligned >1 times 87.99% overall alignment rate Time searching: 00:05:24 Overall time: 00:05:24 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] 1558035 / 5017993 = 0.3105 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 @ Wed, 22 Jul 2020 14:56:26: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.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 @ Wed, 22 Jul 2020 14:56:26: #1 read tag files... INFO @ Wed, 22 Jul 2020 14:56:26: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 14:56:33: 1000000 INFO @ Wed, 22 Jul 2020 14:56:39: 2000000 INFO @ Wed, 22 Jul 2020 14:56:45: 3000000 INFO @ Wed, 22 Jul 2020 14:56:51: 4000000 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 @ Wed, 22 Jul 2020 14:56:56: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.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 @ Wed, 22 Jul 2020 14:56:56: #1 read tag files... INFO @ Wed, 22 Jul 2020 14:56:56: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 14:56:58: 5000000 INFO @ Wed, 22 Jul 2020 14:57:04: 1000000 INFO @ Wed, 22 Jul 2020 14:57:05: 6000000 INFO @ Wed, 22 Jul 2020 14:57:12: 2000000 INFO @ Wed, 22 Jul 2020 14:57:13: 7000000 INFO @ Wed, 22 Jul 2020 14:57:13: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 14:57:13: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 14:57:13: #1 total tags in treatment: 3411395 INFO @ Wed, 22 Jul 2020 14:57:13: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 14:57:13: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Jul 2020 14:57:13: #1 tags after filtering in treatment: 2621943 INFO @ Wed, 22 Jul 2020 14:57:13: #1 Redundant rate of treatment: 0.23 INFO @ Wed, 22 Jul 2020 14:57:13: #1 finished! INFO @ Wed, 22 Jul 2020 14:57:13: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 14:57:13: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 14:57:14: #2 number of paired peaks: 49 WARNING @ Wed, 22 Jul 2020 14:57:14: Too few paired peaks (49) 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 @ Wed, 22 Jul 2020 14:57:14: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.05_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/SRX8462181/SRX8462181.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Wed, 22 Jul 2020 14:57:20: 3000000 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 @ Wed, 22 Jul 2020 14:57:26: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.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 @ Wed, 22 Jul 2020 14:57:26: #1 read tag files... INFO @ Wed, 22 Jul 2020 14:57:26: #1 read treatment tags... INFO @ Wed, 22 Jul 2020 14:57:27: 4000000 INFO @ Wed, 22 Jul 2020 14:57:33: 1000000 INFO @ Wed, 22 Jul 2020 14:57:34: 5000000 INFO @ Wed, 22 Jul 2020 14:57:41: 2000000 INFO @ Wed, 22 Jul 2020 14:57:43: 6000000 INFO @ Wed, 22 Jul 2020 14:57:48: 3000000 INFO @ Wed, 22 Jul 2020 14:57:51: 7000000 INFO @ Wed, 22 Jul 2020 14:57:51: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 14:57:51: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 14:57:51: #1 total tags in treatment: 3411395 INFO @ Wed, 22 Jul 2020 14:57:51: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 14:57:51: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Jul 2020 14:57:52: #1 tags after filtering in treatment: 2621943 INFO @ Wed, 22 Jul 2020 14:57:52: #1 Redundant rate of treatment: 0.23 INFO @ Wed, 22 Jul 2020 14:57:52: #1 finished! INFO @ Wed, 22 Jul 2020 14:57:52: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 14:57:52: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 14:57:52: #2 number of paired peaks: 49 WARNING @ Wed, 22 Jul 2020 14:57:52: Too few paired peaks (49) 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 @ Wed, 22 Jul 2020 14:57:52: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.10_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/SRX8462181/SRX8462181.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Wed, 22 Jul 2020 14:57:55: 4000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Wed, 22 Jul 2020 14:58:02: 5000000 BigWig に変換しました。 INFO @ Wed, 22 Jul 2020 14:58:08: 6000000 INFO @ Wed, 22 Jul 2020 14:58:14: 7000000 INFO @ Wed, 22 Jul 2020 14:58:15: #1 tag size is determined as 75 bps INFO @ Wed, 22 Jul 2020 14:58:15: #1 tag size = 75 INFO @ Wed, 22 Jul 2020 14:58:15: #1 total tags in treatment: 3411395 INFO @ Wed, 22 Jul 2020 14:58:15: #1 user defined the maximum tags... INFO @ Wed, 22 Jul 2020 14:58:15: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Jul 2020 14:58:15: #1 tags after filtering in treatment: 2621943 INFO @ Wed, 22 Jul 2020 14:58:15: #1 Redundant rate of treatment: 0.23 INFO @ Wed, 22 Jul 2020 14:58:15: #1 finished! INFO @ Wed, 22 Jul 2020 14:58:15: #2 Build Peak Model... INFO @ Wed, 22 Jul 2020 14:58:15: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Jul 2020 14:58:15: #2 number of paired peaks: 49 WARNING @ Wed, 22 Jul 2020 14:58:15: Too few paired peaks (49) 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 @ Wed, 22 Jul 2020 14:58:15: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.20_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/SRX8462181/SRX8462181.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX8462181/SRX8462181.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling