Job ID = 1298281 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2019-06-03T08:14:14 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 ) 2019-06-03T08:14:14 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 : 18,038,631 reads read : 36,077,262 reads written : 36,077,262 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘fastqDump_tmp*’: 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: 00:06:27 18038631 reads; of these: 18038631 (100.00%) were paired; of these: 17656826 (97.88%) aligned concordantly 0 times 279801 (1.55%) aligned concordantly exactly 1 time 102004 (0.57%) aligned concordantly >1 times ---- 17656826 pairs aligned concordantly 0 times; of these: 901 (0.01%) aligned discordantly 1 time ---- 17655925 pairs aligned 0 times concordantly or discordantly; of these: 35311850 mates make up the pairs; of these: 35089068 (99.37%) aligned 0 times 84626 (0.24%) aligned exactly 1 time 138156 (0.39%) aligned >1 times 2.74% overall alignment rate Time searching: 00:06:28 Overall time: 00:06:28 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_rmdup_core] processing reference chr2L... [bam_rmdup_core] processing reference chr2LHet... [bam_rmdup_core] processing reference chr2R... [bam_rmdup_core] processing reference chr2RHet... [bam_rmdup_core] processing reference chr3L... [bam_rmdup_core] processing reference chr3LHet... [bam_rmdup_core] processing reference chr3R... [bam_rmdup_core] processing reference chr3RHet... [bam_rmdup_core] processing reference chr4... [bam_rmdup_core] processing reference chrM... [bam_rmdup_core] processing reference chrU... [bam_rmdup_core] processing reference chrUextra... [bam_rmdup_core] processing reference chrX... [bam_rmdup_core] processing reference chrXHet... [bam_rmdup_core] processing reference chrYHet... [bam_rmdup_core] 10046 / 373561 = 0.0269 in library ' ' BAM に変換しました。 Bed ファイルを作成中... BedGraph に変換中... INFO @ Mon, 03 Jun 2019 17:35:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.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 @ Mon, 03 Jun 2019 17:35:34: #1 read tag files... INFO @ Mon, 03 Jun 2019 17:35:34: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 17:35:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.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 @ Mon, 03 Jun 2019 17:35:34: #1 read tag files... INFO @ Mon, 03 Jun 2019 17:35:34: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 17:35:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.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 @ Mon, 03 Jun 2019 17:35:34: #1 read tag files... INFO @ Mon, 03 Jun 2019 17:35:34: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 17:35:46: #1 tag size is determined as 71 bps INFO @ Mon, 03 Jun 2019 17:35:46: #1 tag size = 71 INFO @ Mon, 03 Jun 2019 17:35:46: #1 total tags in treatment: 371760 INFO @ Mon, 03 Jun 2019 17:35:46: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 17:35:46: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 17:35:46: #1 tags after filtering in treatment: 366796 INFO @ Mon, 03 Jun 2019 17:35:46: #1 Redundant rate of treatment: 0.01 INFO @ Mon, 03 Jun 2019 17:35:46: #1 finished! INFO @ Mon, 03 Jun 2019 17:35:46: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 17:35:46: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 17:35:47: #2 number of paired peaks: 695 WARNING @ Mon, 03 Jun 2019 17:35:47: Fewer paired peaks (695) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 695 pairs to build model! INFO @ Mon, 03 Jun 2019 17:35:47: start model_add_line... INFO @ Mon, 03 Jun 2019 17:35:47: start X-correlation... INFO @ Mon, 03 Jun 2019 17:35:47: end of X-cor INFO @ Mon, 03 Jun 2019 17:35:47: #2 finished! INFO @ Mon, 03 Jun 2019 17:35:47: #2 predicted fragment length is 108 bps INFO @ Mon, 03 Jun 2019 17:35:47: #2 alternative fragment length(s) may be 108,558 bps INFO @ Mon, 03 Jun 2019 17:35:47: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.05_model.r WARNING @ Mon, 03 Jun 2019 17:35:47: #2 Since the d (108) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 17:35:47: #2 You may need to consider one of the other alternative d(s): 108,558 WARNING @ Mon, 03 Jun 2019 17:35:47: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 03 Jun 2019 17:35:47: #3 Call peaks... INFO @ Mon, 03 Jun 2019 17:35:47: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 17:35:47: #1 tag size is determined as 71 bps INFO @ Mon, 03 Jun 2019 17:35:47: #1 tag size = 71 INFO @ Mon, 03 Jun 2019 17:35:47: #1 total tags in treatment: 371760 INFO @ Mon, 03 Jun 2019 17:35:47: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 17:35:47: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 17:35:47: #1 tags after filtering in treatment: 366796 INFO @ Mon, 03 Jun 2019 17:35:47: #1 Redundant rate of treatment: 0.01 INFO @ Mon, 03 Jun 2019 17:35:47: #1 finished! INFO @ Mon, 03 Jun 2019 17:35:47: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 17:35:47: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 17:35:47: #1 tag size is determined as 71 bps INFO @ Mon, 03 Jun 2019 17:35:47: #1 tag size = 71 INFO @ Mon, 03 Jun 2019 17:35:47: #1 total tags in treatment: 371760 INFO @ Mon, 03 Jun 2019 17:35:47: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 17:35:47: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 17:35:47: #1 tags after filtering in treatment: 366796 INFO @ Mon, 03 Jun 2019 17:35:47: #1 Redundant rate of treatment: 0.01 INFO @ Mon, 03 Jun 2019 17:35:47: #1 finished! INFO @ Mon, 03 Jun 2019 17:35:47: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 17:35:47: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 17:35:47: #2 number of paired peaks: 695 WARNING @ Mon, 03 Jun 2019 17:35:47: Fewer paired peaks (695) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 695 pairs to build model! INFO @ Mon, 03 Jun 2019 17:35:47: start model_add_line... INFO @ Mon, 03 Jun 2019 17:35:47: start X-correlation... INFO @ Mon, 03 Jun 2019 17:35:47: end of X-cor INFO @ Mon, 03 Jun 2019 17:35:47: #2 finished! INFO @ Mon, 03 Jun 2019 17:35:47: #2 predicted fragment length is 108 bps INFO @ Mon, 03 Jun 2019 17:35:47: #2 alternative fragment length(s) may be 108,558 bps INFO @ Mon, 03 Jun 2019 17:35:47: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.20_model.r WARNING @ Mon, 03 Jun 2019 17:35:47: #2 Since the d (108) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 17:35:47: #2 You may need to consider one of the other alternative d(s): 108,558 WARNING @ Mon, 03 Jun 2019 17:35:47: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 03 Jun 2019 17:35:47: #3 Call peaks... INFO @ Mon, 03 Jun 2019 17:35:47: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 17:35:47: #2 number of paired peaks: 695 WARNING @ Mon, 03 Jun 2019 17:35:47: Fewer paired peaks (695) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 695 pairs to build model! INFO @ Mon, 03 Jun 2019 17:35:47: start model_add_line... INFO @ Mon, 03 Jun 2019 17:35:47: start X-correlation... INFO @ Mon, 03 Jun 2019 17:35:47: end of X-cor INFO @ Mon, 03 Jun 2019 17:35:47: #2 finished! INFO @ Mon, 03 Jun 2019 17:35:47: #2 predicted fragment length is 108 bps INFO @ Mon, 03 Jun 2019 17:35:47: #2 alternative fragment length(s) may be 108,558 bps INFO @ Mon, 03 Jun 2019 17:35:47: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.10_model.r WARNING @ Mon, 03 Jun 2019 17:35:47: #2 Since the d (108) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 17:35:47: #2 You may need to consider one of the other alternative d(s): 108,558 WARNING @ Mon, 03 Jun 2019 17:35:47: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 03 Jun 2019 17:35:47: #3 Call peaks... INFO @ Mon, 03 Jun 2019 17:35:47: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 17:35:48: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 17:35:48: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 17:35:48: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.05_peaks.xls INFO @ Mon, 03 Jun 2019 17:35:48: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.05_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 17:35:48: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.05_summits.bed INFO @ Mon, 03 Jun 2019 17:35:48: Done! INFO @ Mon, 03 Jun 2019 17:35:48: #3 Call peaks for each chromosome... pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (91 records, 4 fields): 3 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... INFO @ Mon, 03 Jun 2019 17:35:49: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.20_peaks.xls INFO @ Mon, 03 Jun 2019 17:35:49: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.20_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 17:35:49: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.20_summits.bed INFO @ Mon, 03 Jun 2019 17:35:49: Done! INFO @ Mon, 03 Jun 2019 17:35:49: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.10_peaks.xls INFO @ Mon, 03 Jun 2019 17:35:49: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.10_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 17:35:49: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650899/SRX4650899.10_summits.bed INFO @ Mon, 03 Jun 2019 17:35:49: Done! pass1 - making usageList (2 chroms): 1 millis pass2 - checking and writing primary data (26 records, 4 fields): 1 millis CompletedMACS2peakCalling pass1 - making usageList (5 chroms): 1 millis pass2 - checking and writing primary data (48 records, 4 fields): 2 millis CompletedMACS2peakCalling BigWig に変換しました。