Job ID = 14521718 SRX = ERX4439628 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 3350108 spots for ERR4501557/ERR4501557.sra Written 3350108 spots for ERR4501557/ERR4501557.sra 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: 00:02:42 3350108 reads; of these: 3350108 (100.00%) were paired; of these: 1001123 (29.88%) aligned concordantly 0 times 2047523 (61.12%) aligned concordantly exactly 1 time 301462 (9.00%) aligned concordantly >1 times ---- 1001123 pairs aligned concordantly 0 times; of these: 461862 (46.13%) aligned discordantly 1 time ---- 539261 pairs aligned 0 times concordantly or discordantly; of these: 1078522 mates make up the pairs; of these: 866239 (80.32%) aligned 0 times 66195 (6.14%) aligned exactly 1 time 146088 (13.55%) aligned >1 times 87.07% overall alignment rate Time searching: 00:02:42 Overall time: 00:02:42 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] 51282 / 2780521 = 0.0184 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/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 21:36:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.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, 15 Jan 2022 21:36:34: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:36:34: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:36:40: 1000000 INFO @ Sat, 15 Jan 2022 21:36:47: 2000000 INFO @ Sat, 15 Jan 2022 21:36:53: 3000000 INFO @ Sat, 15 Jan 2022 21:36:59: 4000000 WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 21:37:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.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, 15 Jan 2022 21:37:04: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:37:04: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:37:05: 5000000 INFO @ Sat, 15 Jan 2022 21:37:10: #1 tag size is determined as 100 bps INFO @ Sat, 15 Jan 2022 21:37:10: #1 tag size = 100 INFO @ Sat, 15 Jan 2022 21:37:10: #1 total tags in treatment: 2311131 INFO @ Sat, 15 Jan 2022 21:37:10: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:37:10: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 21:37:10: #1 tags after filtering in treatment: 1871664 INFO @ Sat, 15 Jan 2022 21:37:10: #1 Redundant rate of treatment: 0.19 INFO @ Sat, 15 Jan 2022 21:37:10: #1 finished! INFO @ Sat, 15 Jan 2022 21:37:10: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:37:10: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:37:10: #2 number of paired peaks: 161 WARNING @ Sat, 15 Jan 2022 21:37:10: Fewer paired peaks (161) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 161 pairs to build model! INFO @ Sat, 15 Jan 2022 21:37:10: start model_add_line... INFO @ Sat, 15 Jan 2022 21:37:10: start X-correlation... INFO @ Sat, 15 Jan 2022 21:37:10: end of X-cor INFO @ Sat, 15 Jan 2022 21:37:10: #2 finished! INFO @ Sat, 15 Jan 2022 21:37:10: #2 predicted fragment length is 173 bps INFO @ Sat, 15 Jan 2022 21:37:10: #2 alternative fragment length(s) may be 173 bps INFO @ Sat, 15 Jan 2022 21:37:10: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.05_model.r WARNING @ Sat, 15 Jan 2022 21:37:10: #2 Since the d (173) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 15 Jan 2022 21:37:10: #2 You may need to consider one of the other alternative d(s): 173 WARNING @ Sat, 15 Jan 2022 21:37:10: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 15 Jan 2022 21:37:10: #3 Call peaks... INFO @ Sat, 15 Jan 2022 21:37:10: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Jan 2022 21:37:11: 1000000 INFO @ Sat, 15 Jan 2022 21:37:15: #3 Call peaks for each chromosome... INFO @ Sat, 15 Jan 2022 21:37:17: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.05_peaks.xls INFO @ Sat, 15 Jan 2022 21:37:17: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.05_peaks.narrowPeak INFO @ Sat, 15 Jan 2022 21:37:17: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.05_summits.bed INFO @ Sat, 15 Jan 2022 21:37:17: Done! pass1 - making usageList (17 chroms): 1 millis pass2 - checking and writing primary data (1208 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 21:37:17: 2000000 INFO @ Sat, 15 Jan 2022 21:37:24: 3000000 INFO @ Sat, 15 Jan 2022 21:37:30: 4000000 BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 21:37:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.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, 15 Jan 2022 21:37:34: #1 read tag files... INFO @ Sat, 15 Jan 2022 21:37:34: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 21:37:37: 5000000 INFO @ Sat, 15 Jan 2022 21:37:42: #1 tag size is determined as 100 bps INFO @ Sat, 15 Jan 2022 21:37:42: #1 tag size = 100 INFO @ Sat, 15 Jan 2022 21:37:42: #1 total tags in treatment: 2311131 INFO @ Sat, 15 Jan 2022 21:37:42: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:37:42: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 21:37:42: #1 tags after filtering in treatment: 1871664 INFO @ Sat, 15 Jan 2022 21:37:42: #1 Redundant rate of treatment: 0.19 INFO @ Sat, 15 Jan 2022 21:37:42: #1 finished! INFO @ Sat, 15 Jan 2022 21:37:42: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:37:42: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:37:42: #2 number of paired peaks: 161 WARNING @ Sat, 15 Jan 2022 21:37:42: Fewer paired peaks (161) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 161 pairs to build model! INFO @ Sat, 15 Jan 2022 21:37:42: start model_add_line... INFO @ Sat, 15 Jan 2022 21:37:42: start X-correlation... INFO @ Sat, 15 Jan 2022 21:37:42: end of X-cor INFO @ Sat, 15 Jan 2022 21:37:42: #2 finished! INFO @ Sat, 15 Jan 2022 21:37:42: #2 predicted fragment length is 173 bps INFO @ Sat, 15 Jan 2022 21:37:42: #2 alternative fragment length(s) may be 173 bps INFO @ Sat, 15 Jan 2022 21:37:42: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.10_model.r WARNING @ Sat, 15 Jan 2022 21:37:42: #2 Since the d (173) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 15 Jan 2022 21:37:42: #2 You may need to consider one of the other alternative d(s): 173 WARNING @ Sat, 15 Jan 2022 21:37:42: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 15 Jan 2022 21:37:42: #3 Call peaks... INFO @ Sat, 15 Jan 2022 21:37:42: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Jan 2022 21:37:43: 1000000 INFO @ Sat, 15 Jan 2022 21:37:47: #3 Call peaks for each chromosome... INFO @ Sat, 15 Jan 2022 21:37:48: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.10_peaks.xls INFO @ Sat, 15 Jan 2022 21:37:48: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.10_peaks.narrowPeak INFO @ Sat, 15 Jan 2022 21:37:49: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.10_summits.bed INFO @ Sat, 15 Jan 2022 21:37:49: Done! pass1 - making usageList (17 chroms): 0 millis pass2 - checking and writing primary data (973 records, 4 fields): 4 millis CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 21:37:50: 2000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 21:37:58: 3000000 INFO @ Sat, 15 Jan 2022 21:38:05: 4000000 BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 21:38:13: 5000000 INFO @ Sat, 15 Jan 2022 21:38:19: #1 tag size is determined as 100 bps INFO @ Sat, 15 Jan 2022 21:38:19: #1 tag size = 100 INFO @ Sat, 15 Jan 2022 21:38:19: #1 total tags in treatment: 2311131 INFO @ Sat, 15 Jan 2022 21:38:19: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 21:38:19: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 21:38:19: #1 tags after filtering in treatment: 1871664 INFO @ Sat, 15 Jan 2022 21:38:19: #1 Redundant rate of treatment: 0.19 INFO @ Sat, 15 Jan 2022 21:38:19: #1 finished! INFO @ Sat, 15 Jan 2022 21:38:19: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 21:38:19: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 21:38:19: #2 number of paired peaks: 161 WARNING @ Sat, 15 Jan 2022 21:38:19: Fewer paired peaks (161) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 161 pairs to build model! INFO @ Sat, 15 Jan 2022 21:38:19: start model_add_line... INFO @ Sat, 15 Jan 2022 21:38:19: start X-correlation... INFO @ Sat, 15 Jan 2022 21:38:19: end of X-cor INFO @ Sat, 15 Jan 2022 21:38:19: #2 finished! INFO @ Sat, 15 Jan 2022 21:38:19: #2 predicted fragment length is 173 bps INFO @ Sat, 15 Jan 2022 21:38:19: #2 alternative fragment length(s) may be 173 bps INFO @ Sat, 15 Jan 2022 21:38:19: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.20_model.r WARNING @ Sat, 15 Jan 2022 21:38:19: #2 Since the d (173) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 15 Jan 2022 21:38:19: #2 You may need to consider one of the other alternative d(s): 173 WARNING @ Sat, 15 Jan 2022 21:38:19: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 15 Jan 2022 21:38:19: #3 Call peaks... INFO @ Sat, 15 Jan 2022 21:38:19: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Jan 2022 21:38:24: #3 Call peaks for each chromosome... INFO @ Sat, 15 Jan 2022 21:38:26: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.20_peaks.xls INFO @ Sat, 15 Jan 2022 21:38:26: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.20_peaks.narrowPeak INFO @ Sat, 15 Jan 2022 21:38:26: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX4439628/ERX4439628.20_summits.bed INFO @ Sat, 15 Jan 2022 21:38:26: Done! pass1 - making usageList (17 chroms): 1 millis pass2 - checking and writing primary data (731 records, 4 fields): 52 millis CompletedMACS2peakCalling