Job ID = 10223873 SRX = ERX4439619 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2020-10-15T23:32:48 prefetch.2.10.7: 1) Downloading 'ERR4501548'... 2020-10-15T23:32:48 prefetch.2.10.7: Downloading via HTTPS... 2020-10-15T23:33:32 prefetch.2.10.7: HTTPS download succeed 2020-10-15T23:33:32 prefetch.2.10.7: 'ERR4501548' is valid 2020-10-15T23:33:32 prefetch.2.10.7: 1) 'ERR4501548' was downloaded successfully 2020-10-15T23:34:00 prefetch.2.10.7: 'ERR4501548' has 5 unresolved dependencies 2020-10-15T23:34:00 prefetch.2.10.7: 2) Downloading 'ncbi-acc:NC_001136.8?vdb-ctx=refseq'... 2020-10-15T23:34:00 prefetch.2.10.7: Downloading via HTTPS... 2020-10-15T23:34:12 prefetch.2.10.7: HTTPS download succeed 2020-10-15T23:34:12 prefetch.2.10.7: 2) 'ncbi-acc:NC_001136.8?vdb-ctx=refseq' was downloaded successfully 2020-10-15T23:34:12 prefetch.2.10.7: 3) Downloading 'ncbi-acc:NC_001139.7?vdb-ctx=refseq'... 2020-10-15T23:34:12 prefetch.2.10.7: Downloading via HTTPS... 2020-10-15T23:34:24 prefetch.2.10.7: HTTPS download succeed 2020-10-15T23:34:24 prefetch.2.10.7: 3) 'ncbi-acc:NC_001139.7?vdb-ctx=refseq' was downloaded successfully 2020-10-15T23:34:24 prefetch.2.10.7: 4) Downloading 'ncbi-acc:NC_001144.4?vdb-ctx=refseq'... 2020-10-15T23:34:24 prefetch.2.10.7: Downloading via HTTPS... 2020-10-15T23:34:37 prefetch.2.10.7: HTTPS download succeed 2020-10-15T23:34:37 prefetch.2.10.7: 4) 'ncbi-acc:NC_001144.4?vdb-ctx=refseq' was downloaded successfully 2020-10-15T23:34:37 prefetch.2.10.7: 5) Downloading 'ncbi-acc:NC_001147.5?vdb-ctx=refseq'... 2020-10-15T23:34:37 prefetch.2.10.7: Downloading via HTTPS... 2020-10-15T23:34:49 prefetch.2.10.7: HTTPS download succeed 2020-10-15T23:34:49 prefetch.2.10.7: 5) 'ncbi-acc:NC_001147.5?vdb-ctx=refseq' was downloaded successfully 2020-10-15T23:34:49 prefetch.2.10.7: 6) Downloading 'ncbi-acc:NC_001224.1?vdb-ctx=refseq'... 2020-10-15T23:34:49 prefetch.2.10.7: Downloading via HTTPS... 2020-10-15T23:34:59 prefetch.2.10.7: HTTPS download succeed 2020-10-15T23:34:59 prefetch.2.10.7: 6) 'ncbi-acc:NC_001224.1?vdb-ctx=refseq' was downloaded successfully Read 3434039 spots for ERR4501548/ERR4501548.sra Written 3434039 spots for ERR4501548/ERR4501548.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: 00:02:47 3434039 reads; of these: 3434039 (100.00%) were paired; of these: 970152 (28.25%) aligned concordantly 0 times 2134094 (62.15%) aligned concordantly exactly 1 time 329793 (9.60%) aligned concordantly >1 times ---- 970152 pairs aligned concordantly 0 times; of these: 456969 (47.10%) aligned discordantly 1 time ---- 513183 pairs aligned 0 times concordantly or discordantly; of these: 1026366 mates make up the pairs; of these: 807625 (78.69%) aligned 0 times 61696 (6.01%) aligned exactly 1 time 157045 (15.30%) aligned >1 times 88.24% overall alignment rate Time searching: 00:02:47 Overall time: 00:02:47 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] 43427 / 2889020 = 0.0150 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/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Fri, 16 Oct 2020 08:41:27: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.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, 16 Oct 2020 08:41:27: #1 read tag files... INFO @ Fri, 16 Oct 2020 08:41:27: #1 read treatment tags... INFO @ Fri, 16 Oct 2020 08:41:34: 1000000 INFO @ Fri, 16 Oct 2020 08:41:41: 2000000 INFO @ Fri, 16 Oct 2020 08:41:47: 3000000 INFO @ Fri, 16 Oct 2020 08:41:54: 4000000 WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Fri, 16 Oct 2020 08:41:57: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.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, 16 Oct 2020 08:41:57: #1 read tag files... INFO @ Fri, 16 Oct 2020 08:41:57: #1 read treatment tags... INFO @ Fri, 16 Oct 2020 08:42:01: 5000000 INFO @ Fri, 16 Oct 2020 08:42:06: 1000000 INFO @ Fri, 16 Oct 2020 08:42:08: #1 tag size is determined as 100 bps INFO @ Fri, 16 Oct 2020 08:42:08: #1 tag size = 100 INFO @ Fri, 16 Oct 2020 08:42:08: #1 total tags in treatment: 2427837 INFO @ Fri, 16 Oct 2020 08:42:08: #1 user defined the maximum tags... INFO @ Fri, 16 Oct 2020 08:42:08: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 16 Oct 2020 08:42:08: #1 tags after filtering in treatment: 2156902 INFO @ Fri, 16 Oct 2020 08:42:08: #1 Redundant rate of treatment: 0.11 INFO @ Fri, 16 Oct 2020 08:42:08: #1 finished! INFO @ Fri, 16 Oct 2020 08:42:08: #2 Build Peak Model... INFO @ Fri, 16 Oct 2020 08:42:08: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 16 Oct 2020 08:42:09: #2 number of paired peaks: 117 WARNING @ Fri, 16 Oct 2020 08:42:09: Fewer paired peaks (117) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 117 pairs to build model! INFO @ Fri, 16 Oct 2020 08:42:09: start model_add_line... INFO @ Fri, 16 Oct 2020 08:42:09: start X-correlation... INFO @ Fri, 16 Oct 2020 08:42:09: end of X-cor INFO @ Fri, 16 Oct 2020 08:42:09: #2 finished! INFO @ Fri, 16 Oct 2020 08:42:09: #2 predicted fragment length is 143 bps INFO @ Fri, 16 Oct 2020 08:42:09: #2 alternative fragment length(s) may be 0,113,130,143,179,258,504,517,537,553,570,589 bps INFO @ Fri, 16 Oct 2020 08:42:09: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.05_model.r WARNING @ Fri, 16 Oct 2020 08:42:09: #2 Since the d (143) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Fri, 16 Oct 2020 08:42:09: #2 You may need to consider one of the other alternative d(s): 0,113,130,143,179,258,504,517,537,553,570,589 WARNING @ Fri, 16 Oct 2020 08:42:09: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Fri, 16 Oct 2020 08:42:09: #3 Call peaks... INFO @ Fri, 16 Oct 2020 08:42:09: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 16 Oct 2020 08:42:13: #3 Call peaks for each chromosome... INFO @ Fri, 16 Oct 2020 08:42:14: 2000000 INFO @ Fri, 16 Oct 2020 08:42:15: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.05_peaks.xls INFO @ Fri, 16 Oct 2020 08:42:15: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.05_peaks.narrowPeak INFO @ Fri, 16 Oct 2020 08:42:15: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.05_summits.bed INFO @ Fri, 16 Oct 2020 08:42:15: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (23 records, 4 fields): 1 millis CompletedMACS2peakCalling INFO @ Fri, 16 Oct 2020 08:42:21: 3000000 BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Fri, 16 Oct 2020 08:42:27: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.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, 16 Oct 2020 08:42:27: #1 read tag files... INFO @ Fri, 16 Oct 2020 08:42:27: #1 read treatment tags... INFO @ Fri, 16 Oct 2020 08:42:29: 4000000 INFO @ Fri, 16 Oct 2020 08:42:35: 1000000 INFO @ Fri, 16 Oct 2020 08:42:38: 5000000 INFO @ Fri, 16 Oct 2020 08:42:43: 2000000 INFO @ Fri, 16 Oct 2020 08:42:46: #1 tag size is determined as 100 bps INFO @ Fri, 16 Oct 2020 08:42:46: #1 tag size = 100 INFO @ Fri, 16 Oct 2020 08:42:46: #1 total tags in treatment: 2427837 INFO @ Fri, 16 Oct 2020 08:42:46: #1 user defined the maximum tags... INFO @ Fri, 16 Oct 2020 08:42:46: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 16 Oct 2020 08:42:46: #1 tags after filtering in treatment: 2156902 INFO @ Fri, 16 Oct 2020 08:42:46: #1 Redundant rate of treatment: 0.11 INFO @ Fri, 16 Oct 2020 08:42:46: #1 finished! INFO @ Fri, 16 Oct 2020 08:42:46: #2 Build Peak Model... INFO @ Fri, 16 Oct 2020 08:42:46: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 16 Oct 2020 08:42:46: #2 number of paired peaks: 117 WARNING @ Fri, 16 Oct 2020 08:42:46: Fewer paired peaks (117) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 117 pairs to build model! INFO @ Fri, 16 Oct 2020 08:42:46: start model_add_line... INFO @ Fri, 16 Oct 2020 08:42:46: start X-correlation... INFO @ Fri, 16 Oct 2020 08:42:46: end of X-cor INFO @ Fri, 16 Oct 2020 08:42:46: #2 finished! INFO @ Fri, 16 Oct 2020 08:42:46: #2 predicted fragment length is 143 bps INFO @ Fri, 16 Oct 2020 08:42:46: #2 alternative fragment length(s) may be 0,113,130,143,179,258,504,517,537,553,570,589 bps INFO @ Fri, 16 Oct 2020 08:42:46: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.10_model.r WARNING @ Fri, 16 Oct 2020 08:42:46: #2 Since the d (143) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Fri, 16 Oct 2020 08:42:46: #2 You may need to consider one of the other alternative d(s): 0,113,130,143,179,258,504,517,537,553,570,589 WARNING @ Fri, 16 Oct 2020 08:42:46: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Fri, 16 Oct 2020 08:42:46: #3 Call peaks... INFO @ Fri, 16 Oct 2020 08:42:46: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 16 Oct 2020 08:42:50: #3 Call peaks for each chromosome... INFO @ Fri, 16 Oct 2020 08:42:51: 3000000 INFO @ Fri, 16 Oct 2020 08:42:52: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.10_peaks.xls INFO @ Fri, 16 Oct 2020 08:42:52: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.10_peaks.narrowPeak INFO @ Fri, 16 Oct 2020 08:42:52: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.10_summits.bed INFO @ Fri, 16 Oct 2020 08:42:52: Done! pass1 - making usageList (4 chroms): 0 millis pass2 - checking and writing primary data (12 records, 4 fields): 2 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... INFO @ Fri, 16 Oct 2020 08:42:58: 4000000 INFO @ Fri, 16 Oct 2020 08:43:05: 5000000 BigWig に変換しました。 INFO @ Fri, 16 Oct 2020 08:43:11: #1 tag size is determined as 100 bps INFO @ Fri, 16 Oct 2020 08:43:11: #1 tag size = 100 INFO @ Fri, 16 Oct 2020 08:43:11: #1 total tags in treatment: 2427837 INFO @ Fri, 16 Oct 2020 08:43:11: #1 user defined the maximum tags... INFO @ Fri, 16 Oct 2020 08:43:11: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 16 Oct 2020 08:43:11: #1 tags after filtering in treatment: 2156902 INFO @ Fri, 16 Oct 2020 08:43:11: #1 Redundant rate of treatment: 0.11 INFO @ Fri, 16 Oct 2020 08:43:11: #1 finished! INFO @ Fri, 16 Oct 2020 08:43:11: #2 Build Peak Model... INFO @ Fri, 16 Oct 2020 08:43:11: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 16 Oct 2020 08:43:11: #2 number of paired peaks: 117 WARNING @ Fri, 16 Oct 2020 08:43:11: Fewer paired peaks (117) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 117 pairs to build model! INFO @ Fri, 16 Oct 2020 08:43:11: start model_add_line... INFO @ Fri, 16 Oct 2020 08:43:11: start X-correlation... INFO @ Fri, 16 Oct 2020 08:43:11: end of X-cor INFO @ Fri, 16 Oct 2020 08:43:11: #2 finished! INFO @ Fri, 16 Oct 2020 08:43:11: #2 predicted fragment length is 143 bps INFO @ Fri, 16 Oct 2020 08:43:11: #2 alternative fragment length(s) may be 0,113,130,143,179,258,504,517,537,553,570,589 bps INFO @ Fri, 16 Oct 2020 08:43:11: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.20_model.r WARNING @ Fri, 16 Oct 2020 08:43:11: #2 Since the d (143) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Fri, 16 Oct 2020 08:43:11: #2 You may need to consider one of the other alternative d(s): 0,113,130,143,179,258,504,517,537,553,570,589 WARNING @ Fri, 16 Oct 2020 08:43:11: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Fri, 16 Oct 2020 08:43:11: #3 Call peaks... INFO @ Fri, 16 Oct 2020 08:43:11: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 16 Oct 2020 08:43:16: #3 Call peaks for each chromosome... INFO @ Fri, 16 Oct 2020 08:43:18: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.20_peaks.xls INFO @ Fri, 16 Oct 2020 08:43:18: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.20_peaks.narrowPeak INFO @ Fri, 16 Oct 2020 08:43:18: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX4439619/ERX4439619.20_summits.bed INFO @ Fri, 16 Oct 2020 08:43:18: Done! pass1 - making usageList (1 chroms): 0 millis pass2 - checking and writing primary data (2 records, 4 fields): 1 millis CompletedMACS2peakCalling