Job ID = 2640791 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2019-08-24T10:12:07 fasterq-dump.2.9.6 sys: connection failed while opening file within cryptographic module - mbedtls_ssl_handshake returned -76 ( NET - Reading information from the socket failed ) 2019-08-24T10:12:07 fasterq-dump.2.9.6 sys: connection failed while opening file within cryptographic module - ktls_handshake failed while accessing '165.112.9.235' from '172.19.7.50' 2019-08-24T10:12:07 fasterq-dump.2.9.6 sys: connection failed while opening file within cryptographic module - Failed to create TLS stream for 'sra-download.ncbi.nlm.nih.gov' (165.112.9.235) from '172.19.7.50' 2019-08-24T10:12:07 fasterq-dump.2.9.6 err: connection failed while opening file within cryptographic module - error with https open 'https://sra-download.ncbi.nlm.nih.gov/traces/sra40/SRR/003273/SRR3351887' 2019-08-24T10:12:20 fasterq-dump.2.9.6 err: cmn_iter.c cmn_iter_open_tbl().VDBManagerOpenTableRead( 'SRR3351887' ) -> RC(rcDB,rcMgr,rcOpening,rcTable,rcIncorrect) spots read : 1,176,894 reads read : 1,176,894 reads written : 1,176,894 spots read : 1,403,771 reads read : 1,403,771 reads written : 1,403,771 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: 00:00:14 2580665 reads; of these: 2580665 (100.00%) were unpaired; of these: 2567381 (99.49%) aligned 0 times 354 (0.01%) aligned exactly 1 time 12930 (0.50%) aligned >1 times 0.51% overall alignment rate Time searching: 00:00:14 Overall time: 00:00:14 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_rmdupse_core] 8223 / 13284 = 0.6190 in library ' ' BAM に変換しました。 Bed ファイルを作成中... INFO @ Sat, 24 Aug 2019 19:16:38: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.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, 24 Aug 2019 19:16:38: #1 read tag files... INFO @ Sat, 24 Aug 2019 19:16:38: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 19:16:38: #1 tag size is determined as 76 bps INFO @ Sat, 24 Aug 2019 19:16:38: #1 tag size = 76 INFO @ Sat, 24 Aug 2019 19:16:38: #1 total tags in treatment: 5061 INFO @ Sat, 24 Aug 2019 19:16:38: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 19:16:38: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 24 Aug 2019 19:16:38: #1 tags after filtering in treatment: 5059 INFO @ Sat, 24 Aug 2019 19:16:38: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 19:16:38: #1 finished! INFO @ Sat, 24 Aug 2019 19:16:38: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 19:16:38: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 19:16:38: #2 number of paired peaks: 10 WARNING @ Sat, 24 Aug 2019 19:16:38: Too few paired peaks (10) 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, 24 Aug 2019 19:16:38: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.05_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 24 Aug 2019 19:17:08: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.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, 24 Aug 2019 19:17:08: #1 read tag files... INFO @ Sat, 24 Aug 2019 19:17:08: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 19:17:08: #1 tag size is determined as 76 bps INFO @ Sat, 24 Aug 2019 19:17:08: #1 tag size = 76 INFO @ Sat, 24 Aug 2019 19:17:08: #1 total tags in treatment: 5061 INFO @ Sat, 24 Aug 2019 19:17:08: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 19:17:08: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 24 Aug 2019 19:17:08: #1 tags after filtering in treatment: 5059 INFO @ Sat, 24 Aug 2019 19:17:08: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 19:17:08: #1 finished! INFO @ Sat, 24 Aug 2019 19:17:08: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 19:17:08: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 19:17:08: #2 number of paired peaks: 10 WARNING @ Sat, 24 Aug 2019 19:17:08: Too few paired peaks (10) 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, 24 Aug 2019 19:17:08: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.10_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/SRX1630037/SRX1630037.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換中... BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 INFO @ Sat, 24 Aug 2019 19:17:38: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.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, 24 Aug 2019 19:17:38: #1 read tag files... INFO @ Sat, 24 Aug 2019 19:17:38: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 19:17:38: #1 tag size is determined as 76 bps INFO @ Sat, 24 Aug 2019 19:17:38: #1 tag size = 76 INFO @ Sat, 24 Aug 2019 19:17:38: #1 total tags in treatment: 5061 INFO @ Sat, 24 Aug 2019 19:17:38: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 19:17:38: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 24 Aug 2019 19:17:38: #1 tags after filtering in treatment: 5059 INFO @ Sat, 24 Aug 2019 19:17:38: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 19:17:38: #1 finished! INFO @ Sat, 24 Aug 2019 19:17:38: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 19:17:38: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 19:17:38: #2 number of paired peaks: 10 WARNING @ Sat, 24 Aug 2019 19:17:38: Too few paired peaks (10) 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, 24 Aug 2019 19:17:38: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.20_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1630037/SRX1630037.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling