Job ID = 2007733 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2019-07-05T07:24:41 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 ) 2019-07-05T07:25:27 fasterq-dump.2.9.6 err: index.c get_nearest_offset() -> too many rounds pos = 24 of 40 2019-07-05T07:25:28 fasterq-dump.2.9.6 err: index.c get_nearest_offset() -> too many rounds pos = 24 of 40 spots read : 16,929 reads read : 33,858 reads written : 33,858 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: 00:00:00 16929 reads; of these: 16929 (100.00%) were paired; of these: 2400 (14.18%) aligned concordantly 0 times 13548 (80.03%) aligned concordantly exactly 1 time 981 (5.79%) aligned concordantly >1 times ---- 2400 pairs aligned concordantly 0 times; of these: 1115 (46.46%) aligned discordantly 1 time ---- 1285 pairs aligned 0 times concordantly or discordantly; of these: 2570 mates make up the pairs; of these: 2030 (78.99%) aligned 0 times 329 (12.80%) aligned exactly 1 time 211 (8.21%) aligned >1 times 94.00% overall alignment rate Time searching: 00:00:00 Overall time: 00:00:00 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_rmdup_core] processing reference chrI... [bam_rmdup_core] processing reference chrII... [bam_rmdup_core] processing reference chrIII... [bam_rmdup_core] processing reference chrIV... [bam_rmdup_core] processing reference chrIX... [bam_rmdup_core] processing reference chrM... [bam_rmdup_core] processing reference chrV... [bam_rmdup_core] processing reference chrVI... [bam_rmdup_core] processing reference chrVII... [bam_rmdup_core] processing reference chrVIII... [bam_rmdup_core] processing reference chrX... [bam_rmdup_core] processing reference chrXI... [bam_rmdup_core] processing reference chrXII... [bam_rmdup_core] processing reference chrXIII... [bam_rmdup_core] processing reference chrXIV... [bam_rmdup_core] processing reference chrXV... [bam_rmdup_core] processing reference chrXVI... [bam_rmdup_core] 15 / 15528 = 0.0010 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 @ Fri, 05 Jul 2019 16:25:41: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.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 @ Fri, 05 Jul 2019 16:25:41: #1 read tag files... INFO @ Fri, 05 Jul 2019 16:25:41: #1 read treatment tags... BedGraph に変換しました。 BigWig に変換中... INFO @ Fri, 05 Jul 2019 16:25:42: #1 tag size is determined as 25 bps INFO @ Fri, 05 Jul 2019 16:25:42: #1 tag size = 25 INFO @ Fri, 05 Jul 2019 16:25:42: #1 total tags in treatment: 14514 INFO @ Fri, 05 Jul 2019 16:25:42: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 16:25:42: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 16:25:42: #1 tags after filtering in treatment: 14498 INFO @ Fri, 05 Jul 2019 16:25:42: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 16:25:42: #1 finished! INFO @ Fri, 05 Jul 2019 16:25:42: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 16:25:42: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 16:25:42: #2 number of paired peaks: 349 WARNING @ Fri, 05 Jul 2019 16:25:42: Fewer paired peaks (349) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 349 pairs to build model! INFO @ Fri, 05 Jul 2019 16:25:42: start model_add_line... INFO @ Fri, 05 Jul 2019 16:25:42: start X-correlation... INFO @ Fri, 05 Jul 2019 16:25:42: end of X-cor INFO @ Fri, 05 Jul 2019 16:25:42: #2 finished! INFO @ Fri, 05 Jul 2019 16:25:42: #2 predicted fragment length is 271 bps INFO @ Fri, 05 Jul 2019 16:25:42: #2 alternative fragment length(s) may be 228,247,271 bps INFO @ Fri, 05 Jul 2019 16:25:42: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.05_model.r INFO @ Fri, 05 Jul 2019 16:25:42: #3 Call peaks... INFO @ Fri, 05 Jul 2019 16:25:42: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 16:25:42: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 16:25:42: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.05_peaks.xls INFO @ Fri, 05 Jul 2019 16:25:42: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.05_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 16:25:42: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.05_summits.bed INFO @ Fri, 05 Jul 2019 16:25:42: Done! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 16:25:42: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.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 @ Fri, 05 Jul 2019 16:25:42: #1 read tag files... INFO @ Fri, 05 Jul 2019 16:25:42: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 16:25:43: #1 tag size is determined as 25 bps INFO @ Fri, 05 Jul 2019 16:25:43: #1 tag size = 25 INFO @ Fri, 05 Jul 2019 16:25:43: #1 total tags in treatment: 14514 INFO @ Fri, 05 Jul 2019 16:25:43: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 16:25:43: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 16:25:43: #1 tags after filtering in treatment: 14498 INFO @ Fri, 05 Jul 2019 16:25:43: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 16:25:43: #1 finished! INFO @ Fri, 05 Jul 2019 16:25:43: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 16:25:43: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 16:25:43: #2 number of paired peaks: 349 WARNING @ Fri, 05 Jul 2019 16:25:43: Fewer paired peaks (349) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 349 pairs to build model! INFO @ Fri, 05 Jul 2019 16:25:43: start model_add_line... INFO @ Fri, 05 Jul 2019 16:25:43: start X-correlation... INFO @ Fri, 05 Jul 2019 16:25:43: end of X-cor INFO @ Fri, 05 Jul 2019 16:25:43: #2 finished! INFO @ Fri, 05 Jul 2019 16:25:43: #2 predicted fragment length is 271 bps INFO @ Fri, 05 Jul 2019 16:25:43: #2 alternative fragment length(s) may be 228,247,271 bps INFO @ Fri, 05 Jul 2019 16:25:43: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.10_model.r INFO @ Fri, 05 Jul 2019 16:25:43: #3 Call peaks... INFO @ Fri, 05 Jul 2019 16:25:43: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 16:25:43: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 16:25:43: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.10_peaks.xls INFO @ Fri, 05 Jul 2019 16:25:43: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.10_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 16:25:43: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.10_summits.bed INFO @ Fri, 05 Jul 2019 16:25:43: Done! pass1 - making usageList (0 chroms): 69 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) BigWig に変換しました。 INFO @ Fri, 05 Jul 2019 16:25:43: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.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 @ Fri, 05 Jul 2019 16:25:43: #1 read tag files... INFO @ Fri, 05 Jul 2019 16:25:43: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 16:25:44: #1 tag size is determined as 25 bps INFO @ Fri, 05 Jul 2019 16:25:44: #1 tag size = 25 INFO @ Fri, 05 Jul 2019 16:25:44: #1 total tags in treatment: 14514 INFO @ Fri, 05 Jul 2019 16:25:44: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 16:25:44: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 16:25:44: #1 tags after filtering in treatment: 14498 INFO @ Fri, 05 Jul 2019 16:25:44: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 16:25:44: #1 finished! INFO @ Fri, 05 Jul 2019 16:25:44: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 16:25:44: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 16:25:44: #2 number of paired peaks: 349 WARNING @ Fri, 05 Jul 2019 16:25:44: Fewer paired peaks (349) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 349 pairs to build model! INFO @ Fri, 05 Jul 2019 16:25:44: start model_add_line... INFO @ Fri, 05 Jul 2019 16:25:44: start X-correlation... INFO @ Fri, 05 Jul 2019 16:25:44: end of X-cor INFO @ Fri, 05 Jul 2019 16:25:44: #2 finished! INFO @ Fri, 05 Jul 2019 16:25:44: #2 predicted fragment length is 271 bps INFO @ Fri, 05 Jul 2019 16:25:44: #2 alternative fragment length(s) may be 228,247,271 bps INFO @ Fri, 05 Jul 2019 16:25:44: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.20_model.r INFO @ Fri, 05 Jul 2019 16:25:44: #3 Call peaks... INFO @ Fri, 05 Jul 2019 16:25:44: #3 Pre-compute pvalue-qvalue table... CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 16:25:44: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 16:25:44: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.20_peaks.xls INFO @ Fri, 05 Jul 2019 16:25:44: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.20_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 16:25:44: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX433681/ERX433681.20_summits.bed INFO @ Fri, 05 Jul 2019 16:25:44: Done! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling