Job ID = 14521681 SRX = ERX4439611 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 3204286 spots for ERR4501540/ERR4501540.sra Written 3204286 spots for ERR4501540/ERR4501540.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: 00:03:46 3204286 reads; of these: 3204286 (100.00%) were paired; of these: 731242 (22.82%) aligned concordantly 0 times 2061749 (64.34%) aligned concordantly exactly 1 time 411295 (12.84%) aligned concordantly >1 times ---- 731242 pairs aligned concordantly 0 times; of these: 314203 (42.97%) aligned discordantly 1 time ---- 417039 pairs aligned 0 times concordantly or discordantly; of these: 834078 mates make up the pairs; of these: 662252 (79.40%) aligned 0 times 45850 (5.50%) aligned exactly 1 time 125976 (15.10%) aligned >1 times 89.67% overall alignment rate Time searching: 00:03:46 Overall time: 00:03:46 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] 62616 / 2763926 = 0.0227 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 21:32:14: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.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 21:32:14: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:32:14: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:32:21: 1000000 INFO @ Sat, 15 Jan 2022 21:32:27: 2000000 INFO @ Sat, 15 Jan 2022 21:32:33: 3000000 INFO @ Sat, 15 Jan 2022 21:32:40: 4000000 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 21:32:44: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.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 21:32:44: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:32:44: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:32:46: 5000000 INFO @ Sat, 15 Jan 2022 21:32:50: #1 tag size is determined as 100 bps INFO @ Sat, 15 Jan 2022 21:32:50: #1 tag size = 100 INFO @ Sat, 15 Jan 2022 21:32:50: #1 total tags in treatment: 2416835 INFO @ Sat, 15 Jan 2022 21:32:50: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:32:50: #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 21:32:50: #1 tags after filtering in treatment: 2014482 INFO @ Sat, 15 Jan 2022 21:32:50: #1 Redundant rate of treatment: 0.17 INFO @ Sat, 15 Jan 2022 21:32:50: #1 finished! INFO @ Sat, 15 Jan 2022 21:32:50: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:32:50: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:32:50: #2 number of paired peaks: 58 WARNING @ Sat, 15 Jan 2022 21:32:50: Too few paired peaks (58) 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 21:32:50: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.05_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/ERX4439611/ERX4439611.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 21:32:50: 1000000 INFO @ Sat, 15 Jan 2022 21:32:57: 2000000 INFO @ Sat, 15 Jan 2022 21:33:03: 3000000 INFO @ Sat, 15 Jan 2022 21:33:09: 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 21:33:14: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.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 21:33:14: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:33:14: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:33:16: 5000000 INFO @ Sat, 15 Jan 2022 21:33:20: #1 tag size is determined as 100 bps INFO @ Sat, 15 Jan 2022 21:33:20: #1 tag size = 100 INFO @ Sat, 15 Jan 2022 21:33:20: #1 total tags in treatment: 2416835 INFO @ Sat, 15 Jan 2022 21:33:20: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:33:20: #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 21:33:20: #1 tags after filtering in treatment: 2014482 INFO @ Sat, 15 Jan 2022 21:33:20: #1 Redundant rate of treatment: 0.17 INFO @ Sat, 15 Jan 2022 21:33:20: #1 finished! INFO @ Sat, 15 Jan 2022 21:33:20: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:33:20: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:33:20: #2 number of paired peaks: 58 WARNING @ Sat, 15 Jan 2022 21:33:20: Too few paired peaks (58) 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 21:33:20: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.10_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/ERX4439611/ERX4439611.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 21:33:21: 1000000 INFO @ Sat, 15 Jan 2022 21:33:27: 2000000 INFO @ Sat, 15 Jan 2022 21:33:33: 3000000 INFO @ Sat, 15 Jan 2022 21:33:39: 4000000 INFO @ Sat, 15 Jan 2022 21:33:46: 5000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 21:33:50: #1 tag size is determined as 100 bps INFO @ Sat, 15 Jan 2022 21:33:50: #1 tag size = 100 INFO @ Sat, 15 Jan 2022 21:33:50: #1 total tags in treatment: 2416835 INFO @ Sat, 15 Jan 2022 21:33:50: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:33:50: #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 21:33:50: #1 tags after filtering in treatment: 2014482 INFO @ Sat, 15 Jan 2022 21:33:50: #1 Redundant rate of treatment: 0.17 INFO @ Sat, 15 Jan 2022 21:33:50: #1 finished! INFO @ Sat, 15 Jan 2022 21:33:50: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:33:50: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:33:50: #2 number of paired peaks: 58 WARNING @ Sat, 15 Jan 2022 21:33:50: Too few paired peaks (58) 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 21:33:50: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.20_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/ERX4439611/ERX4439611.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX4439611/ERX4439611.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BigWig に変換しました。