Job ID = 12531525 SRX = SRX2997378 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 5273342 spots for SRR5819453/SRR5819453.sra Written 5273342 spots for SRR5819453/SRR5819453.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: 00:04:45 5273342 reads; of these: 5273342 (100.00%) were paired; of these: 2493493 (47.28%) aligned concordantly 0 times 1651001 (31.31%) aligned concordantly exactly 1 time 1128848 (21.41%) aligned concordantly >1 times ---- 2493493 pairs aligned concordantly 0 times; of these: 353870 (14.19%) aligned discordantly 1 time ---- 2139623 pairs aligned 0 times concordantly or discordantly; of these: 4279246 mates make up the pairs; of these: 3625513 (84.72%) aligned 0 times 93686 (2.19%) aligned exactly 1 time 560047 (13.09%) aligned >1 times 65.62% overall alignment rate Time searching: 00:04:45 Overall time: 00:04:45 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] 790220 / 3099783 = 0.2549 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/3.7.1/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 17 Apr 2021 08:10:31: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.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, 17 Apr 2021 08:10:31: #1 read tag files... INFO @ Sat, 17 Apr 2021 08:10:31: #1 read treatment tags... INFO @ Sat, 17 Apr 2021 08:10:36: 1000000 INFO @ Sat, 17 Apr 2021 08:10:41: 2000000 INFO @ Sat, 17 Apr 2021 08:10:46: 3000000 INFO @ Sat, 17 Apr 2021 08:10:53: 4000000 WARNING: Skipping mount /opt/pkg/singularity/3.7.1/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 17 Apr 2021 08:10:58: 5000000 INFO @ Sat, 17 Apr 2021 08:11:00: #1 tag size is determined as 76 bps INFO @ Sat, 17 Apr 2021 08:11:00: #1 tag size = 76 INFO @ Sat, 17 Apr 2021 08:11:00: #1 total tags in treatment: 2042915 INFO @ Sat, 17 Apr 2021 08:11:00: #1 user defined the maximum tags... INFO @ Sat, 17 Apr 2021 08:11:00: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 17 Apr 2021 08:11:00: #1 tags after filtering in treatment: 1144398 INFO @ Sat, 17 Apr 2021 08:11:00: #1 Redundant rate of treatment: 0.44 INFO @ Sat, 17 Apr 2021 08:11:00: #1 finished! INFO @ Sat, 17 Apr 2021 08:11:00: #2 Build Peak Model... INFO @ Sat, 17 Apr 2021 08:11:00: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 17 Apr 2021 08:11:00: #2 number of paired peaks: 239 WARNING @ Sat, 17 Apr 2021 08:11:00: Fewer paired peaks (239) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 239 pairs to build model! INFO @ Sat, 17 Apr 2021 08:11:00: start model_add_line... INFO @ Sat, 17 Apr 2021 08:11:00: start X-correlation... INFO @ Sat, 17 Apr 2021 08:11:00: end of X-cor INFO @ Sat, 17 Apr 2021 08:11:00: #2 finished! INFO @ Sat, 17 Apr 2021 08:11:00: #2 predicted fragment length is 87 bps INFO @ Sat, 17 Apr 2021 08:11:00: #2 alternative fragment length(s) may be 87 bps INFO @ Sat, 17 Apr 2021 08:11:00: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.05_model.r WARNING @ Sat, 17 Apr 2021 08:11:00: #2 Since the d (87) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 17 Apr 2021 08:11:00: #2 You may need to consider one of the other alternative d(s): 87 WARNING @ Sat, 17 Apr 2021 08:11:00: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 17 Apr 2021 08:11:00: #3 Call peaks... INFO @ Sat, 17 Apr 2021 08:11:00: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 17 Apr 2021 08:11:01: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.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, 17 Apr 2021 08:11:01: #1 read tag files... INFO @ Sat, 17 Apr 2021 08:11:01: #1 read treatment tags... INFO @ Sat, 17 Apr 2021 08:11:03: #3 Call peaks for each chromosome... INFO @ Sat, 17 Apr 2021 08:11:04: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.05_peaks.xls INFO @ Sat, 17 Apr 2021 08:11:04: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.05_peaks.narrowPeak INFO @ Sat, 17 Apr 2021 08:11:04: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.05_summits.bed INFO @ Sat, 17 Apr 2021 08:11:04: Done! pass1 - making usageList (17 chroms): 1 millis pass2 - checking and writing primary data (1816 records, 4 fields): 4 millis CompletedMACS2peakCalling INFO @ Sat, 17 Apr 2021 08:11:06: 1000000 INFO @ Sat, 17 Apr 2021 08:11:11: 2000000 INFO @ Sat, 17 Apr 2021 08:11:16: 3000000 INFO @ Sat, 17 Apr 2021 08:11:22: 4000000 INFO @ Sat, 17 Apr 2021 08:11:27: 5000000 BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.7.1/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 17 Apr 2021 08:11:29: #1 tag size is determined as 76 bps INFO @ Sat, 17 Apr 2021 08:11:29: #1 tag size = 76 INFO @ Sat, 17 Apr 2021 08:11:29: #1 total tags in treatment: 2042915 INFO @ Sat, 17 Apr 2021 08:11:29: #1 user defined the maximum tags... INFO @ Sat, 17 Apr 2021 08:11:29: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 17 Apr 2021 08:11:29: #1 tags after filtering in treatment: 1144398 INFO @ Sat, 17 Apr 2021 08:11:29: #1 Redundant rate of treatment: 0.44 INFO @ Sat, 17 Apr 2021 08:11:29: #1 finished! INFO @ Sat, 17 Apr 2021 08:11:29: #2 Build Peak Model... INFO @ Sat, 17 Apr 2021 08:11:29: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 17 Apr 2021 08:11:29: #2 number of paired peaks: 239 WARNING @ Sat, 17 Apr 2021 08:11:29: Fewer paired peaks (239) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 239 pairs to build model! INFO @ Sat, 17 Apr 2021 08:11:29: start model_add_line... INFO @ Sat, 17 Apr 2021 08:11:29: start X-correlation... INFO @ Sat, 17 Apr 2021 08:11:29: end of X-cor INFO @ Sat, 17 Apr 2021 08:11:29: #2 finished! INFO @ Sat, 17 Apr 2021 08:11:29: #2 predicted fragment length is 87 bps INFO @ Sat, 17 Apr 2021 08:11:29: #2 alternative fragment length(s) may be 87 bps INFO @ Sat, 17 Apr 2021 08:11:29: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.10_model.r WARNING @ Sat, 17 Apr 2021 08:11:29: #2 Since the d (87) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 17 Apr 2021 08:11:29: #2 You may need to consider one of the other alternative d(s): 87 WARNING @ Sat, 17 Apr 2021 08:11:29: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 17 Apr 2021 08:11:29: #3 Call peaks... INFO @ Sat, 17 Apr 2021 08:11:29: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 17 Apr 2021 08:11:31: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.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, 17 Apr 2021 08:11:31: #1 read tag files... INFO @ Sat, 17 Apr 2021 08:11:31: #1 read treatment tags... INFO @ Sat, 17 Apr 2021 08:11:32: #3 Call peaks for each chromosome... INFO @ Sat, 17 Apr 2021 08:11:33: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.10_peaks.xls INFO @ Sat, 17 Apr 2021 08:11:33: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.10_peaks.narrowPeak INFO @ Sat, 17 Apr 2021 08:11:33: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.10_summits.bed INFO @ Sat, 17 Apr 2021 08:11:33: Done! pass1 - making usageList (17 chroms): 1 millis pass2 - checking and writing primary data (997 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Sat, 17 Apr 2021 08:11:36: 1000000 INFO @ Sat, 17 Apr 2021 08:11:41: 2000000 INFO @ Sat, 17 Apr 2021 08:11:47: 3000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 17 Apr 2021 08:11:52: 4000000 INFO @ Sat, 17 Apr 2021 08:11:57: 5000000 BigWig に変換しました。 INFO @ Sat, 17 Apr 2021 08:11:59: #1 tag size is determined as 76 bps INFO @ Sat, 17 Apr 2021 08:11:59: #1 tag size = 76 INFO @ Sat, 17 Apr 2021 08:11:59: #1 total tags in treatment: 2042915 INFO @ Sat, 17 Apr 2021 08:11:59: #1 user defined the maximum tags... INFO @ Sat, 17 Apr 2021 08:11:59: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 17 Apr 2021 08:11:59: #1 tags after filtering in treatment: 1144398 INFO @ Sat, 17 Apr 2021 08:11:59: #1 Redundant rate of treatment: 0.44 INFO @ Sat, 17 Apr 2021 08:11:59: #1 finished! INFO @ Sat, 17 Apr 2021 08:11:59: #2 Build Peak Model... INFO @ Sat, 17 Apr 2021 08:11:59: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 17 Apr 2021 08:11:59: #2 number of paired peaks: 239 WARNING @ Sat, 17 Apr 2021 08:11:59: Fewer paired peaks (239) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 239 pairs to build model! INFO @ Sat, 17 Apr 2021 08:11:59: start model_add_line... INFO @ Sat, 17 Apr 2021 08:11:59: start X-correlation... INFO @ Sat, 17 Apr 2021 08:11:59: end of X-cor INFO @ Sat, 17 Apr 2021 08:11:59: #2 finished! INFO @ Sat, 17 Apr 2021 08:11:59: #2 predicted fragment length is 87 bps INFO @ Sat, 17 Apr 2021 08:11:59: #2 alternative fragment length(s) may be 87 bps INFO @ Sat, 17 Apr 2021 08:11:59: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.20_model.r WARNING @ Sat, 17 Apr 2021 08:11:59: #2 Since the d (87) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 17 Apr 2021 08:11:59: #2 You may need to consider one of the other alternative d(s): 87 WARNING @ Sat, 17 Apr 2021 08:11:59: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 17 Apr 2021 08:11:59: #3 Call peaks... INFO @ Sat, 17 Apr 2021 08:11:59: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 17 Apr 2021 08:12:01: #3 Call peaks for each chromosome... INFO @ Sat, 17 Apr 2021 08:12:02: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.20_peaks.xls INFO @ Sat, 17 Apr 2021 08:12:02: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.20_peaks.narrowPeak INFO @ Sat, 17 Apr 2021 08:12:02: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/SRX2997378/SRX2997378.20_summits.bed INFO @ Sat, 17 Apr 2021 08:12:02: Done! pass1 - making usageList (17 chroms): 0 millis pass2 - checking and writing primary data (367 records, 4 fields): 3 millis CompletedMACS2peakCalling