Job ID = 14171267 SRX = SRX9005655 Genome = dm3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Rejected 812467 READS because READLEN < 1 Read 4516085 spots for SRR12515056/SRR12515056.sra Written 4516085 spots for SRR12515056/SRR12515056.sra fastq に変換しました。 bowtie でマッピング中... Your job 14171740 ("srTdm6") has been submitted Time loading reference: 00:00:00 Time loading forward index: 00:00:00 Time loading mirror index: 00:00:00 Error, fewer reads in file specified with -2 than in file specified with -1 terminate called after throwing an instance of 'int' (ERR): bowtie2-align died with signal 6 (ABRT) (core dumped) 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_sort_core] merging from 8 files... [bam_rmdup_core] processing reference chr2L... [bam_rmdup_core] processing reference chr2LHet... [bam_rmdup_core] processing reference chr2R... [bam_rmdup_core] 1 unmatched pairs [bam_rmdup_core] processing reference chr2RHet... [bam_rmdup_core] 2 unmatched pairs [bam_rmdup_core] processing reference chr3L... [bam_rmdup_core] processing reference chr3LHet... [bam_rmdup_core] processing reference chr3R... [bam_rmdup_core] 4 unmatched pairs [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] 14 unmatched pairs [bam_rmdup_core] processing reference chrX... [bam_rmdup_core] processing reference chrXHet... [bam_rmdup_core] processing reference chrYHet... [bam_rmdup_core] 428090 / 3346186 = 0.1279 in library ' ' awk: cmd. line:1: (FILENAME=- FNR=1) fatal: division by zero attempted 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, 11 Dec 2021 11:07:29: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.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 @ Sat, 11 Dec 2021 11:07:29: #1 read tag files... INFO @ Sat, 11 Dec 2021 11:07:29: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 11:07:37: 1000000 INFO @ Sat, 11 Dec 2021 11:07:46: 2000000 INFO @ Sat, 11 Dec 2021 11:07:54: 3000000 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, 11 Dec 2021 11:07:59: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.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 @ Sat, 11 Dec 2021 11:07:59: #1 read tag files... INFO @ Sat, 11 Dec 2021 11:07:59: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 11:08:02: 4000000 INFO @ Sat, 11 Dec 2021 11:08:08: 1000000 INFO @ Sat, 11 Dec 2021 11:08:10: 5000000 INFO @ Sat, 11 Dec 2021 11:08:17: 2000000 INFO @ Sat, 11 Dec 2021 11:08:18: 6000000 INFO @ Sat, 11 Dec 2021 11:08:23: #1 tag size is determined as 125 bps INFO @ Sat, 11 Dec 2021 11:08:23: #1 tag size = 125 INFO @ Sat, 11 Dec 2021 11:08:23: #1 total tags in treatment: 2853538 INFO @ Sat, 11 Dec 2021 11:08:23: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 11:08:23: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 11 Dec 2021 11:08:23: #1 tags after filtering in treatment: 2365687 INFO @ Sat, 11 Dec 2021 11:08:23: #1 Redundant rate of treatment: 0.17 INFO @ Sat, 11 Dec 2021 11:08:23: #1 finished! INFO @ Sat, 11 Dec 2021 11:08:23: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 11:08:23: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 11:08:24: #2 number of paired peaks: 6775 INFO @ Sat, 11 Dec 2021 11:08:24: start model_add_line... INFO @ Sat, 11 Dec 2021 11:08:24: start X-correlation... INFO @ Sat, 11 Dec 2021 11:08:24: end of X-cor INFO @ Sat, 11 Dec 2021 11:08:24: #2 finished! INFO @ Sat, 11 Dec 2021 11:08:24: #2 predicted fragment length is 222 bps INFO @ Sat, 11 Dec 2021 11:08:24: #2 alternative fragment length(s) may be 222 bps INFO @ Sat, 11 Dec 2021 11:08:24: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.05_model.r WARNING @ Sat, 11 Dec 2021 11:08:24: #2 Since the d (222) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 11:08:24: #2 You may need to consider one of the other alternative d(s): 222 WARNING @ Sat, 11 Dec 2021 11:08:24: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 11 Dec 2021 11:08:24: #3 Call peaks... INFO @ Sat, 11 Dec 2021 11:08:24: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 11:08:26: 3000000 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, 11 Dec 2021 11:08:29: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.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 @ Sat, 11 Dec 2021 11:08:29: #1 read tag files... INFO @ Sat, 11 Dec 2021 11:08:29: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 11:08:32: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 11:08:35: 4000000 INFO @ Sat, 11 Dec 2021 11:08:36: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.05_peaks.xls INFO @ Sat, 11 Dec 2021 11:08:36: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.05_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 11:08:36: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.05_summits.bed INFO @ Sat, 11 Dec 2021 11:08:36: Done! pass1 - making usageList (15 chroms): 2 millis pass2 - checking and writing primary data (7551 records, 4 fields): 11 millis CompletedMACS2peakCalling INFO @ Sat, 11 Dec 2021 11:08:39: 1000000 INFO @ Sat, 11 Dec 2021 11:08:44: 5000000 INFO @ Sat, 11 Dec 2021 11:08:48: 2000000 INFO @ Sat, 11 Dec 2021 11:08:53: 6000000 INFO @ Sat, 11 Dec 2021 11:08:57: 3000000 INFO @ Sat, 11 Dec 2021 11:08:59: #1 tag size is determined as 125 bps INFO @ Sat, 11 Dec 2021 11:08:59: #1 tag size = 125 INFO @ Sat, 11 Dec 2021 11:08:59: #1 total tags in treatment: 2853538 INFO @ Sat, 11 Dec 2021 11:08:59: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 11:08:59: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 11 Dec 2021 11:08:59: #1 tags after filtering in treatment: 2365687 INFO @ Sat, 11 Dec 2021 11:08:59: #1 Redundant rate of treatment: 0.17 INFO @ Sat, 11 Dec 2021 11:08:59: #1 finished! INFO @ Sat, 11 Dec 2021 11:08:59: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 11:08:59: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 11:08:59: #2 number of paired peaks: 6775 INFO @ Sat, 11 Dec 2021 11:08:59: start model_add_line... INFO @ Sat, 11 Dec 2021 11:08:59: start X-correlation... INFO @ Sat, 11 Dec 2021 11:08:59: end of X-cor INFO @ Sat, 11 Dec 2021 11:08:59: #2 finished! INFO @ Sat, 11 Dec 2021 11:08:59: #2 predicted fragment length is 222 bps INFO @ Sat, 11 Dec 2021 11:08:59: #2 alternative fragment length(s) may be 222 bps INFO @ Sat, 11 Dec 2021 11:08:59: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.10_model.r WARNING @ Sat, 11 Dec 2021 11:08:59: #2 Since the d (222) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 11:08:59: #2 You may need to consider one of the other alternative d(s): 222 WARNING @ Sat, 11 Dec 2021 11:08:59: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 11 Dec 2021 11:08:59: #3 Call peaks... INFO @ Sat, 11 Dec 2021 11:08:59: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 11:09:06: 4000000 INFO @ Sat, 11 Dec 2021 11:09:08: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 11:09:12: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.10_peaks.xls INFO @ Sat, 11 Dec 2021 11:09:12: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.10_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 11:09:12: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.10_summits.bed INFO @ Sat, 11 Dec 2021 11:09:12: Done! pass1 - making usageList (15 chroms): 2 millis pass2 - checking and writing primary data (5647 records, 4 fields): 10 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 11 Dec 2021 11:09:15: 5000000 INFO @ Sat, 11 Dec 2021 11:09:23: 6000000 BigWig に変換しました。 INFO @ Sat, 11 Dec 2021 11:09:28: #1 tag size is determined as 125 bps INFO @ Sat, 11 Dec 2021 11:09:28: #1 tag size = 125 INFO @ Sat, 11 Dec 2021 11:09:28: #1 total tags in treatment: 2853538 INFO @ Sat, 11 Dec 2021 11:09:28: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 11:09:28: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 11 Dec 2021 11:09:29: #1 tags after filtering in treatment: 2365687 INFO @ Sat, 11 Dec 2021 11:09:29: #1 Redundant rate of treatment: 0.17 INFO @ Sat, 11 Dec 2021 11:09:29: #1 finished! INFO @ Sat, 11 Dec 2021 11:09:29: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 11:09:29: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 11:09:29: #2 number of paired peaks: 6775 INFO @ Sat, 11 Dec 2021 11:09:29: start model_add_line... INFO @ Sat, 11 Dec 2021 11:09:29: start X-correlation... INFO @ Sat, 11 Dec 2021 11:09:29: end of X-cor INFO @ Sat, 11 Dec 2021 11:09:29: #2 finished! INFO @ Sat, 11 Dec 2021 11:09:29: #2 predicted fragment length is 222 bps INFO @ Sat, 11 Dec 2021 11:09:29: #2 alternative fragment length(s) may be 222 bps INFO @ Sat, 11 Dec 2021 11:09:29: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.20_model.r WARNING @ Sat, 11 Dec 2021 11:09:29: #2 Since the d (222) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 11:09:29: #2 You may need to consider one of the other alternative d(s): 222 WARNING @ Sat, 11 Dec 2021 11:09:29: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 11 Dec 2021 11:09:29: #3 Call peaks... INFO @ Sat, 11 Dec 2021 11:09:29: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 11:09:37: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 11:09:41: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.20_peaks.xls INFO @ Sat, 11 Dec 2021 11:09:41: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.20_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 11:09:41: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX9005655/SRX9005655.20_summits.bed INFO @ Sat, 11 Dec 2021 11:09:41: Done! pass1 - making usageList (15 chroms): 2 millis pass2 - checking and writing primary data (3795 records, 4 fields): 8 millis CompletedMACS2peakCalling