Job ID = 5791037 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2020-04-21T23:19:17 fasterq-dump.2.9.6 sys: timeout exhausted while reading file within network system module - mbedtls_ssl_read returned -76 ( NET - Reading information from the socket failed ) 2020-04-21T23:19:17 fasterq-dump.2.9.6 sys: timeout exhausted while reading file within network system module - mbedtls_ssl_read returned -76 ( NET - Reading information from the socket failed ) 2020-04-21T23:19:17 fasterq-dump.2.9.6 sys: timeout exhausted while reading file within network system module - mbedtls_ssl_read returned -76 ( NET - Reading information from the socket failed ) spots read : 3,604,310 reads read : 7,208,620 reads written : 7,208,620 rm: cannot remove ‘[DSE]RR*’: No such file or directory 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: 00:01:24 3604310 reads; of these: 3604310 (100.00%) were paired; of these: 787289 (21.84%) aligned concordantly 0 times 2425423 (67.29%) aligned concordantly exactly 1 time 391598 (10.86%) aligned concordantly >1 times ---- 787289 pairs aligned concordantly 0 times; of these: 138962 (17.65%) aligned discordantly 1 time ---- 648327 pairs aligned 0 times concordantly or discordantly; of these: 1296654 mates make up the pairs; of these: 973071 (75.04%) aligned 0 times 246336 (19.00%) aligned exactly 1 time 77247 (5.96%) aligned >1 times 86.50% overall alignment rate Time searching: 00:01:24 Overall time: 00:01:24 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_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] 77807 / 2931722 = 0.0265 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 Apr 2020 08:23:43: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.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 Apr 2020 08:23:43: #1 read tag files... INFO @ Wed, 22 Apr 2020 08:23:43: #1 read treatment tags... INFO @ Wed, 22 Apr 2020 08:23:49: 1000000 INFO @ Wed, 22 Apr 2020 08:23:54: 2000000 INFO @ Wed, 22 Apr 2020 08:24:00: 3000000 INFO @ Wed, 22 Apr 2020 08:24:05: 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 Apr 2020 08:24:11: 5000000 INFO @ Wed, 22 Apr 2020 08:24:14: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.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 Apr 2020 08:24:14: #1 read tag files... INFO @ Wed, 22 Apr 2020 08:24:14: #1 read treatment tags... INFO @ Wed, 22 Apr 2020 08:24:17: 6000000 INFO @ Wed, 22 Apr 2020 08:24:17: #1 tag size is determined as 37 bps INFO @ Wed, 22 Apr 2020 08:24:17: #1 tag size = 37 INFO @ Wed, 22 Apr 2020 08:24:17: #1 total tags in treatment: 2743117 INFO @ Wed, 22 Apr 2020 08:24:17: #1 user defined the maximum tags... INFO @ Wed, 22 Apr 2020 08:24:17: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Apr 2020 08:24:17: #1 tags after filtering in treatment: 2234760 INFO @ Wed, 22 Apr 2020 08:24:17: #1 Redundant rate of treatment: 0.19 INFO @ Wed, 22 Apr 2020 08:24:17: #1 finished! INFO @ Wed, 22 Apr 2020 08:24:17: #2 Build Peak Model... INFO @ Wed, 22 Apr 2020 08:24:17: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Apr 2020 08:24:18: #2 number of paired peaks: 34 WARNING @ Wed, 22 Apr 2020 08:24:18: Too few paired peaks (34) 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 Apr 2020 08:24:18: Process for pairing-model is terminated! INFO @ Wed, 22 Apr 2020 08:24:19: 1000000 cut: /home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.05_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/SRX5883261/SRX5883261.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Wed, 22 Apr 2020 08:24:24: 2000000 INFO @ Wed, 22 Apr 2020 08:24:29: 3000000 INFO @ Wed, 22 Apr 2020 08:24:34: 4000000 INFO @ Wed, 22 Apr 2020 08:24:39: 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 @ Wed, 22 Apr 2020 08:24:43: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.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 Apr 2020 08:24:43: #1 read tag files... INFO @ Wed, 22 Apr 2020 08:24:43: #1 read treatment tags... INFO @ Wed, 22 Apr 2020 08:24:44: 6000000 INFO @ Wed, 22 Apr 2020 08:24:44: #1 tag size is determined as 37 bps INFO @ Wed, 22 Apr 2020 08:24:44: #1 tag size = 37 INFO @ Wed, 22 Apr 2020 08:24:44: #1 total tags in treatment: 2743117 INFO @ Wed, 22 Apr 2020 08:24:44: #1 user defined the maximum tags... INFO @ Wed, 22 Apr 2020 08:24:44: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Apr 2020 08:24:44: #1 tags after filtering in treatment: 2234760 INFO @ Wed, 22 Apr 2020 08:24:44: #1 Redundant rate of treatment: 0.19 INFO @ Wed, 22 Apr 2020 08:24:44: #1 finished! INFO @ Wed, 22 Apr 2020 08:24:44: #2 Build Peak Model... INFO @ Wed, 22 Apr 2020 08:24:44: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Apr 2020 08:24:44: #2 number of paired peaks: 34 WARNING @ Wed, 22 Apr 2020 08:24:44: Too few paired peaks (34) 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 Apr 2020 08:24:44: Process for pairing-model is terminated! INFO @ Wed, 22 Apr 2020 08:24:48: 1000000 cut: /home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.10_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/SRX5883261/SRX5883261.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Wed, 22 Apr 2020 08:24:54: 2000000 INFO @ Wed, 22 Apr 2020 08:24:59: 3000000 INFO @ Wed, 22 Apr 2020 08:25:04: 4000000 INFO @ Wed, 22 Apr 2020 08:25:09: 5000000 INFO @ Wed, 22 Apr 2020 08:25:14: 6000000 INFO @ Wed, 22 Apr 2020 08:25:14: #1 tag size is determined as 37 bps INFO @ Wed, 22 Apr 2020 08:25:14: #1 tag size = 37 INFO @ Wed, 22 Apr 2020 08:25:14: #1 total tags in treatment: 2743117 INFO @ Wed, 22 Apr 2020 08:25:14: #1 user defined the maximum tags... INFO @ Wed, 22 Apr 2020 08:25:14: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 22 Apr 2020 08:25:14: #1 tags after filtering in treatment: 2234760 INFO @ Wed, 22 Apr 2020 08:25:14: #1 Redundant rate of treatment: 0.19 INFO @ Wed, 22 Apr 2020 08:25:14: #1 finished! INFO @ Wed, 22 Apr 2020 08:25:14: #2 Build Peak Model... INFO @ Wed, 22 Apr 2020 08:25:14: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 22 Apr 2020 08:25:14: #2 number of paired peaks: 34 WARNING @ Wed, 22 Apr 2020 08:25:14: Too few paired peaks (34) 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 Apr 2020 08:25:14: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.20_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/SRX5883261/SRX5883261.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5883261/SRX5883261.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。