Job ID = 1298229 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2019-06-03T08:14:03 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 ) 2019-06-03T08:14:03 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 ) 2019-06-03T08:24:14 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 ) 2019-06-03T08:38:44 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 ) 2019-06-03T08:40:02 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 ) 2019-06-03T08:41:52 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 ) 2019-06-03T08:46:28 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 ) 2019-06-03T08:48:21 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 ) spots read : 42,041,544 reads read : 84,083,088 reads written : 84,083,088 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘fastqDump_tmp*’: 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: 00:11:40 42041544 reads; of these: 42041544 (100.00%) were paired; of these: 41583835 (98.91%) aligned concordantly 0 times 362795 (0.86%) aligned concordantly exactly 1 time 94914 (0.23%) aligned concordantly >1 times ---- 41583835 pairs aligned concordantly 0 times; of these: 934 (0.00%) aligned discordantly 1 time ---- 41582901 pairs aligned 0 times concordantly or discordantly; of these: 83165802 mates make up the pairs; of these: 82749910 (99.50%) aligned 0 times 110790 (0.13%) aligned exactly 1 time 305102 (0.37%) aligned >1 times 1.59% overall alignment rate Time searching: 00:11:40 Overall time: 00:11:40 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_rmdup_core] processing reference chr2L... [bam_rmdup_core] processing reference chr2LHet... [bam_rmdup_core] processing reference chr2R... [bam_rmdup_core] processing reference chr2RHet... [bam_rmdup_core] processing reference chr3L... [bam_rmdup_core] processing reference chr3LHet... [bam_rmdup_core] processing reference chr3R... [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] processing reference chrX... [bam_rmdup_core] processing reference chrXHet... [bam_rmdup_core] processing reference chrYHet... [bam_rmdup_core] 12397 / 442636 = 0.0280 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 @ Mon, 03 Jun 2019 18:08:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.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 @ Mon, 03 Jun 2019 18:08:30: #1 read tag files... INFO @ Mon, 03 Jun 2019 18:08:30: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 18:08:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.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 @ Mon, 03 Jun 2019 18:08:30: #1 read tag files... INFO @ Mon, 03 Jun 2019 18:08:30: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 18:08:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.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 @ Mon, 03 Jun 2019 18:08:30: #1 read tag files... INFO @ Mon, 03 Jun 2019 18:08:30: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 18:08:37: 1000000 INFO @ Mon, 03 Jun 2019 18:08:38: 1000000 INFO @ Mon, 03 Jun 2019 18:08:39: #1 tag size is determined as 79 bps INFO @ Mon, 03 Jun 2019 18:08:39: #1 tag size = 79 INFO @ Mon, 03 Jun 2019 18:08:39: #1 total tags in treatment: 445318 INFO @ Mon, 03 Jun 2019 18:08:39: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 18:08:39: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 18:08:39: #1 tags after filtering in treatment: 436952 INFO @ Mon, 03 Jun 2019 18:08:39: #1 Redundant rate of treatment: 0.02 INFO @ Mon, 03 Jun 2019 18:08:39: #1 finished! INFO @ Mon, 03 Jun 2019 18:08:39: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 18:08:39: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 18:08:39: #2 number of paired peaks: 2454 INFO @ Mon, 03 Jun 2019 18:08:39: start model_add_line... INFO @ Mon, 03 Jun 2019 18:08:39: start X-correlation... INFO @ Mon, 03 Jun 2019 18:08:39: end of X-cor INFO @ Mon, 03 Jun 2019 18:08:39: #2 finished! INFO @ Mon, 03 Jun 2019 18:08:39: #2 predicted fragment length is 135 bps INFO @ Mon, 03 Jun 2019 18:08:39: #2 alternative fragment length(s) may be 135,151 bps INFO @ Mon, 03 Jun 2019 18:08:39: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.20_model.r WARNING @ Mon, 03 Jun 2019 18:08:39: #2 Since the d (135) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 18:08:39: #2 You may need to consider one of the other alternative d(s): 135,151 WARNING @ Mon, 03 Jun 2019 18:08:39: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 03 Jun 2019 18:08:39: #3 Call peaks... INFO @ Mon, 03 Jun 2019 18:08:39: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 18:08:39: 1000000 INFO @ Mon, 03 Jun 2019 18:08:40: #1 tag size is determined as 79 bps INFO @ Mon, 03 Jun 2019 18:08:40: #1 tag size = 79 INFO @ Mon, 03 Jun 2019 18:08:40: #1 total tags in treatment: 445318 INFO @ Mon, 03 Jun 2019 18:08:40: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 18:08:40: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 18:08:40: #1 tags after filtering in treatment: 436952 INFO @ Mon, 03 Jun 2019 18:08:40: #1 Redundant rate of treatment: 0.02 INFO @ Mon, 03 Jun 2019 18:08:40: #1 finished! INFO @ Mon, 03 Jun 2019 18:08:40: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 18:08:40: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 18:08:40: #2 number of paired peaks: 2454 INFO @ Mon, 03 Jun 2019 18:08:40: start model_add_line... INFO @ Mon, 03 Jun 2019 18:08:40: start X-correlation... INFO @ Mon, 03 Jun 2019 18:08:40: end of X-cor INFO @ Mon, 03 Jun 2019 18:08:40: #2 finished! INFO @ Mon, 03 Jun 2019 18:08:40: #2 predicted fragment length is 135 bps INFO @ Mon, 03 Jun 2019 18:08:40: #2 alternative fragment length(s) may be 135,151 bps INFO @ Mon, 03 Jun 2019 18:08:40: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.10_model.r WARNING @ Mon, 03 Jun 2019 18:08:40: #2 Since the d (135) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 18:08:40: #2 You may need to consider one of the other alternative d(s): 135,151 WARNING @ Mon, 03 Jun 2019 18:08:40: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 03 Jun 2019 18:08:40: #3 Call peaks... INFO @ Mon, 03 Jun 2019 18:08:40: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 18:08:40: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 18:08:41: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.20_peaks.xls INFO @ Mon, 03 Jun 2019 18:08:41: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.20_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 18:08:41: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.20_summits.bed INFO @ Mon, 03 Jun 2019 18:08:41: Done! pass1 - making usageList (3 chroms): 1 millis pass2 - checking and writing primary data (32 records, 4 fields): 1 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 18:08:41: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 18:08:42: #1 tag size is determined as 79 bps INFO @ Mon, 03 Jun 2019 18:08:42: #1 tag size = 79 INFO @ Mon, 03 Jun 2019 18:08:42: #1 total tags in treatment: 445318 INFO @ Mon, 03 Jun 2019 18:08:42: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 18:08:42: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 18:08:42: #1 tags after filtering in treatment: 436952 INFO @ Mon, 03 Jun 2019 18:08:42: #1 Redundant rate of treatment: 0.02 INFO @ Mon, 03 Jun 2019 18:08:42: #1 finished! INFO @ Mon, 03 Jun 2019 18:08:42: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 18:08:42: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 18:08:42: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.10_peaks.xls INFO @ Mon, 03 Jun 2019 18:08:42: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.10_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 18:08:42: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.10_summits.bed INFO @ Mon, 03 Jun 2019 18:08:42: Done! INFO @ Mon, 03 Jun 2019 18:08:42: #2 number of paired peaks: 2454 INFO @ Mon, 03 Jun 2019 18:08:42: start model_add_line... INFO @ Mon, 03 Jun 2019 18:08:42: start X-correlation... pass1 - making usageList (7 chroms): 2 millis pass2 - checking and writing primary data (101 records, 4 fields): 1 millis INFO @ Mon, 03 Jun 2019 18:08:42: end of X-cor INFO @ Mon, 03 Jun 2019 18:08:42: #2 finished! INFO @ Mon, 03 Jun 2019 18:08:42: #2 predicted fragment length is 135 bps INFO @ Mon, 03 Jun 2019 18:08:42: #2 alternative fragment length(s) may be 135,151 bps INFO @ Mon, 03 Jun 2019 18:08:42: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.05_model.r CompletedMACS2peakCalling WARNING @ Mon, 03 Jun 2019 18:08:42: #2 Since the d (135) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 18:08:42: #2 You may need to consider one of the other alternative d(s): 135,151 WARNING @ Mon, 03 Jun 2019 18:08:42: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 03 Jun 2019 18:08:42: #3 Call peaks... INFO @ Mon, 03 Jun 2019 18:08:42: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 18:08:44: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 18:08:44: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.05_peaks.xls INFO @ Mon, 03 Jun 2019 18:08:44: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.05_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 18:08:44: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650895/SRX4650895.05_summits.bed INFO @ Mon, 03 Jun 2019 18:08:44: Done! pass1 - making usageList (10 chroms): 1 millis pass2 - checking and writing primary data (235 records, 4 fields): 2 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。