Job ID = 5720739 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-04-15T16:05:24 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 ) 2020-04-15T16:05:24 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 ) 2020-04-15T16:05:24 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 : 5,711,649 reads read : 11,423,298 reads written : 5,711,649 reads 0-length : 5,711,649 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: 00:05:29 5711649 reads; of these: 5711649 (100.00%) were unpaired; of these: 906854 (15.88%) aligned 0 times 1303695 (22.83%) aligned exactly 1 time 3501100 (61.30%) aligned >1 times 84.12% overall alignment rate Time searching: 00:05:29 Overall time: 00:05:29 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 15 sequences. [bam_rmdupse_core] 1827950 / 4804795 = 0.3804 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 @ Thu, 16 Apr 2020 01:15:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Thu, 16 Apr 2020 01:15:04: #1 read tag files... INFO @ Thu, 16 Apr 2020 01:15:04: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 01:15:10: 1000000 INFO @ Thu, 16 Apr 2020 01:15:16: 2000000 INFO @ Thu, 16 Apr 2020 01:15:23: #1 tag size is determined as 75 bps INFO @ Thu, 16 Apr 2020 01:15:23: #1 tag size = 75 INFO @ Thu, 16 Apr 2020 01:15:23: #1 total tags in treatment: 2976845 INFO @ Thu, 16 Apr 2020 01:15:23: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 01:15:23: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 16 Apr 2020 01:15:23: #1 tags after filtering in treatment: 2976845 INFO @ Thu, 16 Apr 2020 01:15:23: #1 Redundant rate of treatment: 0.00 INFO @ Thu, 16 Apr 2020 01:15:23: #1 finished! INFO @ Thu, 16 Apr 2020 01:15:23: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 01:15:23: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 01:15:23: #2 number of paired peaks: 3811 INFO @ Thu, 16 Apr 2020 01:15:23: start model_add_line... INFO @ Thu, 16 Apr 2020 01:15:23: start X-correlation... INFO @ Thu, 16 Apr 2020 01:15:23: end of X-cor INFO @ Thu, 16 Apr 2020 01:15:23: #2 finished! INFO @ Thu, 16 Apr 2020 01:15:23: #2 predicted fragment length is 90 bps INFO @ Thu, 16 Apr 2020 01:15:23: #2 alternative fragment length(s) may be 90 bps INFO @ Thu, 16 Apr 2020 01:15:23: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.05_model.r WARNING @ Thu, 16 Apr 2020 01:15:23: #2 Since the d (90) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 16 Apr 2020 01:15:23: #2 You may need to consider one of the other alternative d(s): 90 WARNING @ Thu, 16 Apr 2020 01:15:23: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Thu, 16 Apr 2020 01:15:23: #3 Call peaks... INFO @ Thu, 16 Apr 2020 01:15:23: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 01:15:30: #3 Call peaks for each chromosome... 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 @ Thu, 16 Apr 2020 01:15:33: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.05_peaks.xls INFO @ Thu, 16 Apr 2020 01:15:33: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.05_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 01:15:33: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.05_summits.bed INFO @ Thu, 16 Apr 2020 01:15:33: Done! pass1 - making usageList (15 chroms): 1 millis pass2 - checking and writing primary data (4498 records, 4 fields): 5 millis CompletedMACS2peakCalling INFO @ Thu, 16 Apr 2020 01:15:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Thu, 16 Apr 2020 01:15:34: #1 read tag files... INFO @ Thu, 16 Apr 2020 01:15:34: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 01:15:40: 1000000 INFO @ Thu, 16 Apr 2020 01:15:46: 2000000 INFO @ Thu, 16 Apr 2020 01:15:52: #1 tag size is determined as 75 bps INFO @ Thu, 16 Apr 2020 01:15:52: #1 tag size = 75 INFO @ Thu, 16 Apr 2020 01:15:52: #1 total tags in treatment: 2976845 INFO @ Thu, 16 Apr 2020 01:15:52: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 01:15:52: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 16 Apr 2020 01:15:52: #1 tags after filtering in treatment: 2976845 INFO @ Thu, 16 Apr 2020 01:15:52: #1 Redundant rate of treatment: 0.00 INFO @ Thu, 16 Apr 2020 01:15:52: #1 finished! INFO @ Thu, 16 Apr 2020 01:15:52: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 01:15:52: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 01:15:53: #2 number of paired peaks: 3811 INFO @ Thu, 16 Apr 2020 01:15:53: start model_add_line... INFO @ Thu, 16 Apr 2020 01:15:53: start X-correlation... INFO @ Thu, 16 Apr 2020 01:15:53: end of X-cor INFO @ Thu, 16 Apr 2020 01:15:53: #2 finished! INFO @ Thu, 16 Apr 2020 01:15:53: #2 predicted fragment length is 90 bps INFO @ Thu, 16 Apr 2020 01:15:53: #2 alternative fragment length(s) may be 90 bps INFO @ Thu, 16 Apr 2020 01:15:53: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.10_model.r WARNING @ Thu, 16 Apr 2020 01:15:53: #2 Since the d (90) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 16 Apr 2020 01:15:53: #2 You may need to consider one of the other alternative d(s): 90 WARNING @ Thu, 16 Apr 2020 01:15:53: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Thu, 16 Apr 2020 01:15:53: #3 Call peaks... INFO @ Thu, 16 Apr 2020 01:15:53: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 01:15:59: #3 Call peaks for each chromosome... 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 @ Thu, 16 Apr 2020 01:16:02: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.10_peaks.xls INFO @ Thu, 16 Apr 2020 01:16:02: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.10_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 01:16:02: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.10_summits.bed INFO @ Thu, 16 Apr 2020 01:16:02: Done! pass1 - making usageList (15 chroms): 1 millis pass2 - checking and writing primary data (2708 records, 4 fields): 4 millis CompletedMACS2peakCalling INFO @ Thu, 16 Apr 2020 01:16:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Thu, 16 Apr 2020 01:16:04: #1 read tag files... INFO @ Thu, 16 Apr 2020 01:16:04: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 01:16:10: 1000000 INFO @ Thu, 16 Apr 2020 01:16:16: 2000000 INFO @ Thu, 16 Apr 2020 01:16:22: #1 tag size is determined as 75 bps INFO @ Thu, 16 Apr 2020 01:16:22: #1 tag size = 75 INFO @ Thu, 16 Apr 2020 01:16:22: #1 total tags in treatment: 2976845 INFO @ Thu, 16 Apr 2020 01:16:22: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 01:16:22: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 16 Apr 2020 01:16:22: #1 tags after filtering in treatment: 2976845 INFO @ Thu, 16 Apr 2020 01:16:22: #1 Redundant rate of treatment: 0.00 INFO @ Thu, 16 Apr 2020 01:16:22: #1 finished! INFO @ Thu, 16 Apr 2020 01:16:22: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 01:16:22: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 01:16:23: #2 number of paired peaks: 3811 INFO @ Thu, 16 Apr 2020 01:16:23: start model_add_line... INFO @ Thu, 16 Apr 2020 01:16:23: start X-correlation... INFO @ Thu, 16 Apr 2020 01:16:23: end of X-cor INFO @ Thu, 16 Apr 2020 01:16:23: #2 finished! INFO @ Thu, 16 Apr 2020 01:16:23: #2 predicted fragment length is 90 bps INFO @ Thu, 16 Apr 2020 01:16:23: #2 alternative fragment length(s) may be 90 bps INFO @ Thu, 16 Apr 2020 01:16:23: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.20_model.r WARNING @ Thu, 16 Apr 2020 01:16:23: #2 Since the d (90) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 16 Apr 2020 01:16:23: #2 You may need to consider one of the other alternative d(s): 90 WARNING @ Thu, 16 Apr 2020 01:16:23: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Thu, 16 Apr 2020 01:16:23: #3 Call peaks... INFO @ Thu, 16 Apr 2020 01:16:23: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 01:16:29: #3 Call peaks for each chromosome... INFO @ Thu, 16 Apr 2020 01:16:32: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.20_peaks.xls INFO @ Thu, 16 Apr 2020 01:16:32: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.20_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 01:16:32: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX5226978/SRX5226978.20_summits.bed INFO @ Thu, 16 Apr 2020 01:16:32: Done! pass1 - making usageList (14 chroms): 0 millis pass2 - checking and writing primary data (1438 records, 4 fields): 3 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。