Job ID = 1297556 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2019-06-03T08:00:54 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 ) 2019-06-03T08:11:19 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 ) 2019-06-03T08:11:19 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 : 35,329,600 reads read : 70,659,200 reads written : 70,659,200 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: 00:05:54 35329600 reads; of these: 35329600 (100.00%) were paired; of these: 35049021 (99.21%) aligned concordantly 0 times 221099 (0.63%) aligned concordantly exactly 1 time 59480 (0.17%) aligned concordantly >1 times ---- 35049021 pairs aligned concordantly 0 times; of these: 899 (0.00%) aligned discordantly 1 time ---- 35048122 pairs aligned 0 times concordantly or discordantly; of these: 70096244 mates make up the pairs; of these: 69580420 (99.26%) aligned 0 times 125197 (0.18%) aligned exactly 1 time 390627 (0.56%) aligned >1 times 1.53% overall alignment rate Time searching: 00:05:54 Overall time: 00:05:54 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] 8836 / 280435 = 0.0315 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 17:19:47: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.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 17:19:47: #1 read tag files... INFO @ Mon, 03 Jun 2019 17:19:47: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 17:19:47: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.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 17:19:47: #1 read tag files... INFO @ Mon, 03 Jun 2019 17:19:47: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 17:19:47: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.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 17:19:47: #1 read tag files... INFO @ Mon, 03 Jun 2019 17:19:47: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 17:19:55: 1000000 INFO @ Mon, 03 Jun 2019 17:19:55: 1000000 INFO @ Mon, 03 Jun 2019 17:19:55: #1 tag size is determined as 39 bps INFO @ Mon, 03 Jun 2019 17:19:55: #1 tag size = 39 INFO @ Mon, 03 Jun 2019 17:19:55: #1 total tags in treatment: 271773 INFO @ Mon, 03 Jun 2019 17:19:55: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 17:19:55: #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 17:19:55: #1 tags after filtering in treatment: 267644 INFO @ Mon, 03 Jun 2019 17:19:55: #1 Redundant rate of treatment: 0.02 INFO @ Mon, 03 Jun 2019 17:19:55: #1 finished! INFO @ Mon, 03 Jun 2019 17:19:55: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 17:19:55: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 17:19:55: #2 number of paired peaks: 2510 INFO @ Mon, 03 Jun 2019 17:19:55: start model_add_line... INFO @ Mon, 03 Jun 2019 17:19:55: start X-correlation... INFO @ Mon, 03 Jun 2019 17:19:55: end of X-cor INFO @ Mon, 03 Jun 2019 17:19:55: #2 finished! INFO @ Mon, 03 Jun 2019 17:19:55: #2 predicted fragment length is 193 bps INFO @ Mon, 03 Jun 2019 17:19:55: #2 alternative fragment length(s) may be 50,104,144,193 bps INFO @ Mon, 03 Jun 2019 17:19:55: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.05_model.r INFO @ Mon, 03 Jun 2019 17:19:55: #3 Call peaks... INFO @ Mon, 03 Jun 2019 17:19:55: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 17:19:55: #1 tag size is determined as 39 bps INFO @ Mon, 03 Jun 2019 17:19:55: #1 tag size = 39 INFO @ Mon, 03 Jun 2019 17:19:55: #1 total tags in treatment: 271773 INFO @ Mon, 03 Jun 2019 17:19:55: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 17:19:55: #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 17:19:56: #1 tags after filtering in treatment: 267644 INFO @ Mon, 03 Jun 2019 17:19:56: #1 Redundant rate of treatment: 0.02 INFO @ Mon, 03 Jun 2019 17:19:56: #1 finished! INFO @ Mon, 03 Jun 2019 17:19:56: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 17:19:56: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 17:19:56: #2 number of paired peaks: 2510 INFO @ Mon, 03 Jun 2019 17:19:56: start model_add_line... INFO @ Mon, 03 Jun 2019 17:19:56: start X-correlation... INFO @ Mon, 03 Jun 2019 17:19:56: end of X-cor INFO @ Mon, 03 Jun 2019 17:19:56: #2 finished! INFO @ Mon, 03 Jun 2019 17:19:56: #2 predicted fragment length is 193 bps INFO @ Mon, 03 Jun 2019 17:19:56: #2 alternative fragment length(s) may be 50,104,144,193 bps INFO @ Mon, 03 Jun 2019 17:19:56: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.20_model.r INFO @ Mon, 03 Jun 2019 17:19:56: #3 Call peaks... INFO @ Mon, 03 Jun 2019 17:19:56: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 17:19:56: 1000000 INFO @ Mon, 03 Jun 2019 17:19:56: #1 tag size is determined as 39 bps INFO @ Mon, 03 Jun 2019 17:19:56: #1 tag size = 39 INFO @ Mon, 03 Jun 2019 17:19:56: #1 total tags in treatment: 271773 INFO @ Mon, 03 Jun 2019 17:19:56: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 17:19:56: #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 17:19:56: #1 tags after filtering in treatment: 267644 INFO @ Mon, 03 Jun 2019 17:19:56: #1 Redundant rate of treatment: 0.02 INFO @ Mon, 03 Jun 2019 17:19:56: #1 finished! INFO @ Mon, 03 Jun 2019 17:19:56: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 17:19:56: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 17:19:56: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 17:19:56: #2 number of paired peaks: 2510 INFO @ Mon, 03 Jun 2019 17:19:56: start model_add_line... INFO @ Mon, 03 Jun 2019 17:19:56: start X-correlation... INFO @ Mon, 03 Jun 2019 17:19:56: end of X-cor INFO @ Mon, 03 Jun 2019 17:19:56: #2 finished! INFO @ Mon, 03 Jun 2019 17:19:56: #2 predicted fragment length is 193 bps INFO @ Mon, 03 Jun 2019 17:19:56: #2 alternative fragment length(s) may be 50,104,144,193 bps INFO @ Mon, 03 Jun 2019 17:19:56: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.10_model.r INFO @ Mon, 03 Jun 2019 17:19:56: #3 Call peaks... INFO @ Mon, 03 Jun 2019 17:19:56: #3 Pre-compute pvalue-qvalue table... BedGraph に変換しました。 BigWig に変換中... INFO @ Mon, 03 Jun 2019 17:19:57: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 17:19:57: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.05_peaks.xls INFO @ Mon, 03 Jun 2019 17:19:57: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.05_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 17:19:57: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.05_summits.bed INFO @ Mon, 03 Jun 2019 17:19:57: Done! pass1 - making usageList (8 chroms): 1 millis pass2 - checking and writing primary data (124 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 17:19:57: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.20_peaks.xls INFO @ Mon, 03 Jun 2019 17:19:57: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.20_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 17:19:57: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.20_summits.bed INFO @ Mon, 03 Jun 2019 17:19:57: Done! pass1 - making usageList (2 chroms): 1 millis pass2 - checking and writing primary data (7 records, 4 fields): 1 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 17:19:57: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 17:19:58: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.10_peaks.xls INFO @ Mon, 03 Jun 2019 17:19:58: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.10_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 17:19:58: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650859/SRX4650859.10_summits.bed INFO @ Mon, 03 Jun 2019 17:19:58: Done! pass1 - making usageList (8 chroms): 1 millis pass2 - checking and writing primary data (46 records, 4 fields): 1 millis CompletedMACS2peakCalling BigWig に変換しました。