Job ID = 14522046 SRX = SRX9773813 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 1817538 spots for SRR13347754/SRR13347754.sra Written 1817538 spots for SRR13347754/SRR13347754.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: 00:00:37 1817538 reads; of these: 1817538 (100.00%) were paired; of these: 970575 (53.40%) aligned concordantly 0 times 591599 (32.55%) aligned concordantly exactly 1 time 255364 (14.05%) aligned concordantly >1 times ---- 970575 pairs aligned concordantly 0 times; of these: 3738 (0.39%) aligned discordantly 1 time ---- 966837 pairs aligned 0 times concordantly or discordantly; of these: 1933674 mates make up the pairs; of these: 1918792 (99.23%) aligned 0 times 8282 (0.43%) aligned exactly 1 time 6600 (0.34%) aligned >1 times 47.21% overall alignment rate Time searching: 00:00:37 Overall time: 00:00:37 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] 418671 / 850441 = 0.4923 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 22:04:21: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.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 22:04:21: #1 read tag files... INFO @ Sat, 15 Jan 2022 22:04:21: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 22:04:26: #1 tag size is determined as 40 bps INFO @ Sat, 15 Jan 2022 22:04:26: #1 tag size = 40 INFO @ Sat, 15 Jan 2022 22:04:26: #1 total tags in treatment: 429042 INFO @ Sat, 15 Jan 2022 22:04:26: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 22:04:26: #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 22:04:27: #1 tags after filtering in treatment: 320680 INFO @ Sat, 15 Jan 2022 22:04:27: #1 Redundant rate of treatment: 0.25 INFO @ Sat, 15 Jan 2022 22:04:27: #1 finished! INFO @ Sat, 15 Jan 2022 22:04:27: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 22:04:27: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 22:04:27: #2 number of paired peaks: 66 WARNING @ Sat, 15 Jan 2022 22:04:27: Too few paired peaks (66) 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 22:04:27: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.05_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/SRX9773813/SRX9773813.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling 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 22:04:51: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.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 22:04:51: #1 read tag files... INFO @ Sat, 15 Jan 2022 22:04:51: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 22:04:56: #1 tag size is determined as 40 bps INFO @ Sat, 15 Jan 2022 22:04:56: #1 tag size = 40 INFO @ Sat, 15 Jan 2022 22:04:56: #1 total tags in treatment: 429042 INFO @ Sat, 15 Jan 2022 22:04:56: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 22:04:56: #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 22:04:56: #1 tags after filtering in treatment: 320680 INFO @ Sat, 15 Jan 2022 22:04:56: #1 Redundant rate of treatment: 0.25 INFO @ Sat, 15 Jan 2022 22:04:56: #1 finished! INFO @ Sat, 15 Jan 2022 22:04:56: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 22:04:56: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 22:04:56: #2 number of paired peaks: 66 WARNING @ Sat, 15 Jan 2022 22:04:56: Too few paired peaks (66) 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 22:04:56: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.10_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/SRX9773813/SRX9773813.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling 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 22:05:21: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.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 22:05:21: #1 read tag files... INFO @ Sat, 15 Jan 2022 22:05:21: #1 read treatment tags... BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 22:05:26: #1 tag size is determined as 40 bps INFO @ Sat, 15 Jan 2022 22:05:26: #1 tag size = 40 INFO @ Sat, 15 Jan 2022 22:05:26: #1 total tags in treatment: 429042 INFO @ Sat, 15 Jan 2022 22:05:26: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 22:05:26: #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 22:05:26: #1 tags after filtering in treatment: 320680 INFO @ Sat, 15 Jan 2022 22:05:26: #1 Redundant rate of treatment: 0.25 INFO @ Sat, 15 Jan 2022 22:05:26: #1 finished! INFO @ Sat, 15 Jan 2022 22:05:26: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 22:05:26: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 22:05:26: #2 number of paired peaks: 66 WARNING @ Sat, 15 Jan 2022 22:05:26: Too few paired peaks (66) 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 22:05:26: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.20_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/SRX9773813/SRX9773813.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX9773813/SRX9773813.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling