Job ID = 2640787 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 2,710,391 reads read : 2,710,391 reads written : 2,710,391 2019-08-24T10:12:04 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 ) 2019-08-24T10:12:04 fasterq-dump.2.9.6 sys: connection failed while opening file within cryptographic module - ktls_handshake failed while accessing '165.112.9.235' from '172.19.7.45' 2019-08-24T10:12:04 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 '172.19.7.45' 2019-08-24T10:12:04 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/sos/sra-pub-run-1/SRR3351618/SRR3351618.1' 2019-08-24T10:12:04 fasterq-dump.2.9.6 err: invalid accession 'SRR3351618' spots read : 2,064,988 reads read : 2,064,988 reads written : 2,064,988 rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR3351617.sra.cache’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR3351618.sra.cache’: 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: 00:00:24 4775379 reads; of these: 4775379 (100.00%) were unpaired; of these: 4756187 (99.60%) aligned 0 times 826 (0.02%) aligned exactly 1 time 18366 (0.38%) aligned >1 times 0.40% overall alignment rate Time searching: 00:00:24 Overall time: 00:00:24 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_rmdupse_core] 14080 / 19192 = 0.7336 in library ' ' BAM に変換しました。 Bed ファイルを作成中... INFO @ Sat, 24 Aug 2019 19:14:36: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.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 19:14:36: #1 read tag files... INFO @ Sat, 24 Aug 2019 19:14:36: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 19:14:36: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 19:14:36: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 19:14:36: #1 total tags in treatment: 5112 INFO @ Sat, 24 Aug 2019 19:14:36: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 19:14:36: #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 19:14:36: #1 tags after filtering in treatment: 5112 INFO @ Sat, 24 Aug 2019 19:14:36: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 19:14:36: #1 finished! INFO @ Sat, 24 Aug 2019 19:14:36: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 19:14:36: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 19:14:36: #2 number of paired peaks: 27 WARNING @ Sat, 24 Aug 2019 19:14:36: 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, 24 Aug 2019 19:14:36: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.05_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/SRX1629957/SRX1629957.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 24 Aug 2019 19:15:05: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.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 19:15:05: #1 read tag files... INFO @ Sat, 24 Aug 2019 19:15:05: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 19:15:05: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 19:15:05: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 19:15:05: #1 total tags in treatment: 5112 INFO @ Sat, 24 Aug 2019 19:15:05: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 19:15:05: #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 19:15:05: #1 tags after filtering in treatment: 5112 INFO @ Sat, 24 Aug 2019 19:15:05: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 19:15:05: #1 finished! INFO @ Sat, 24 Aug 2019 19:15:05: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 19:15:05: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 19:15:05: #2 number of paired peaks: 27 WARNING @ Sat, 24 Aug 2019 19:15:05: 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, 24 Aug 2019 19:15:05: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.10_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/SRX1629957/SRX1629957.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.10_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 19:15:35: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.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 19:15:35: #1 read tag files... INFO @ Sat, 24 Aug 2019 19:15:35: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 19:15:35: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 19:15:35: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 19:15:35: #1 total tags in treatment: 5112 INFO @ Sat, 24 Aug 2019 19:15:35: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 19:15:35: #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 19:15:35: #1 tags after filtering in treatment: 5112 INFO @ Sat, 24 Aug 2019 19:15:35: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 19:15:35: #1 finished! INFO @ Sat, 24 Aug 2019 19:15:35: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 19:15:35: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 19:15:35: #2 number of paired peaks: 27 WARNING @ Sat, 24 Aug 2019 19:15:35: 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, 24 Aug 2019 19:15:35: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.20_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/SRX1629957/SRX1629957.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1629957/SRX1629957.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling