Job ID = 14520196 SRX = SRX7496395 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 1936267 spots for SRR10823006/SRR10823006.sra Written 1936267 spots for SRR10823006/SRR10823006.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: 00:00:55 1936267 reads; of these: 1936267 (100.00%) were paired; of these: 902238 (46.60%) aligned concordantly 0 times 892501 (46.09%) aligned concordantly exactly 1 time 141528 (7.31%) aligned concordantly >1 times ---- 902238 pairs aligned concordantly 0 times; of these: 15100 (1.67%) aligned discordantly 1 time ---- 887138 pairs aligned 0 times concordantly or discordantly; of these: 1774276 mates make up the pairs; of these: 1004171 (56.60%) aligned 0 times 658736 (37.13%) aligned exactly 1 time 111369 (6.28%) aligned >1 times 74.07% overall alignment rate Time searching: 00:00:55 Overall time: 00:00:55 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] 29387 / 1048976 = 0.0280 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 18:36:15: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.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 18:36:15: #1 read tag files... INFO @ Sat, 15 Jan 2022 18:36:15: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 18:36:20: 1000000 INFO @ Sat, 15 Jan 2022 18:36:25: 2000000 INFO @ Sat, 15 Jan 2022 18:36:29: #1 tag size is determined as 37 bps INFO @ Sat, 15 Jan 2022 18:36:29: #1 tag size = 37 INFO @ Sat, 15 Jan 2022 18:36:29: #1 total tags in treatment: 1004821 INFO @ Sat, 15 Jan 2022 18:36:29: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 18:36:29: #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 18:36:29: #1 tags after filtering in treatment: 856633 INFO @ Sat, 15 Jan 2022 18:36:29: #1 Redundant rate of treatment: 0.15 INFO @ Sat, 15 Jan 2022 18:36:29: #1 finished! INFO @ Sat, 15 Jan 2022 18:36:29: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 18:36:29: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 18:36:29: #2 number of paired peaks: 27 WARNING @ Sat, 15 Jan 2022 18:36:29: Too few paired peaks (27) 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 18:36:29: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.05_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/SRX7496395/SRX7496395.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.05_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 18:36:45: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.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 18:36:45: #1 read tag files... INFO @ Sat, 15 Jan 2022 18:36:45: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 18:36:51: 1000000 INFO @ Sat, 15 Jan 2022 18:36:57: 2000000 INFO @ Sat, 15 Jan 2022 18:37:02: #1 tag size is determined as 37 bps INFO @ Sat, 15 Jan 2022 18:37:02: #1 tag size = 37 INFO @ Sat, 15 Jan 2022 18:37:02: #1 total tags in treatment: 1004821 INFO @ Sat, 15 Jan 2022 18:37:02: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 18:37:02: #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 18:37:02: #1 tags after filtering in treatment: 856633 INFO @ Sat, 15 Jan 2022 18:37:02: #1 Redundant rate of treatment: 0.15 INFO @ Sat, 15 Jan 2022 18:37:02: #1 finished! INFO @ Sat, 15 Jan 2022 18:37:02: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 18:37:02: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 18:37:02: #2 number of paired peaks: 27 WARNING @ Sat, 15 Jan 2022 18:37:02: Too few paired peaks (27) 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 18:37:02: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.10_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/SRX7496395/SRX7496395.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.10_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 18:37:15: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.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 18:37:15: #1 read tag files... INFO @ Sat, 15 Jan 2022 18:37:15: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 18:37:21: 1000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 18:37:27: 2000000 BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 18:37:32: #1 tag size is determined as 37 bps INFO @ Sat, 15 Jan 2022 18:37:32: #1 tag size = 37 INFO @ Sat, 15 Jan 2022 18:37:32: #1 total tags in treatment: 1004821 INFO @ Sat, 15 Jan 2022 18:37:32: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 18:37:32: #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 18:37:32: #1 tags after filtering in treatment: 856633 INFO @ Sat, 15 Jan 2022 18:37:32: #1 Redundant rate of treatment: 0.15 INFO @ Sat, 15 Jan 2022 18:37:32: #1 finished! INFO @ Sat, 15 Jan 2022 18:37:32: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 18:37:32: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 18:37:32: #2 number of paired peaks: 27 WARNING @ Sat, 15 Jan 2022 18:37:32: Too few paired peaks (27) 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 18:37:32: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.20_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/SRX7496395/SRX7496395.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX7496395/SRX7496395.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling