Open Gemma-Zhang-326 opened 3 years ago
And if I set the peaks mode - COMBINED,SELF The results seems too strange
Mon Aug 09 09:24:55 CST 2021: Starting hichipper pipeline v0.7.7
Mon Aug 09 09:24:55 CST 2021: Executed from: /gpfs/home/zhangyue/V1_hic
Mon Aug 09 09:24:55 CST 2021: Output folder: /gpfs/home/zhangyue/V1_hic/V1_loop
Mon Aug 09 09:24:55 CST 2021: Parsed manifest as follows:
{'peaks': ['COMBINED,SELF'], 'hicpro_output': ['hicpro'], 'resfrags': ['/gpfs/home/zhangyue/biosoft/HiCPro/HiC-Pro_3.0.0/annotation/AluI_Mmul_10.bed']}
Mon Aug 09 09:24:55 CST 2021: Determined that the following samples are good to go:
['RM01-V1-2', 'RM01-V1-1']
Mon Aug 09 09:24:55 CST 2021: User defined peaks specification: COMBINED,SELF
Mon Aug 09 09:24:55 CST 2021: Calling one set of peaks from HiChIP self-ligation reads across all samples.
Mon Aug 09 09:24:55 CST 2021: macs2 command: macs2 callpeak -t V1_loop/allDEandSCpairs.bed.tmp --keep-dup all -q 0.01 --extsize 147 --nomodel -g hs -B -f BED --verbose 0 -n V1_loop/allSamples_temporary
Mon Aug 09 09:26:16 CST 2021: Performing restriction fragment-aware padding
Mon Aug 9 09:26:43 CST 2021: Processing RM01-V1-2
Mon Aug 9 09:26:43 CST 2021: Total_PETs=112147382
Mon Aug 9 09:26:49 CST 2021: Mapped_unique_quality_pairs=77830832
Mon Aug 9 09:26:51 CST 2021: Mapped_unique_quality_valid_pairs=35044129
Mon Aug 9 09:26:51 CST 2021: Intersecting PETs with anchors
Mon Aug 9 09:26:52 CST 2021: Finished the anchor merging.
Mon Aug 9 09:26:52 CST 2021: Finished the anchor processing.
Mon Aug 9 09:42:12 CST 2021: Intrachromosomal_valid_small=2025473
Mon Aug 9 09:42:44 CST 2021: Intrachromosomal_valid_med=7076666
Mon Aug 9 09:43:07 CST 2021: Intrachromosomal_valid_large=6888506
Mon Aug 9 09:43:07 CST 2021: Total number of anchors used: 450
Mon Aug 9 09:43:07 CST 2021: Total number of reads in anchors: 63738
Mon Aug 9 09:44:16 CST 2021: Mapped_unique_intra_quality_anchor=147
Mon Aug 9 09:44:16 CST 2021: Mapped_unique_intra_quality_anchor_small=145
Mon Aug 9 09:44:16 CST 2021: Mapped_unique_intra_quality_anchor_med=1
Mon Aug 9 09:44:16 CST 2021: Mapped_unique_intra_quality_anchor_large=1
Mon Aug 9 09:44:16 CST 2021: Loop_PETs=1
Mon Aug 9 09:44:16 CST 2021: Processing RM01-V1-1
Mon Aug 9 09:44:16 CST 2021: Total_PETs=132494051
Mon Aug 9 09:44:23 CST 2021: Mapped_unique_quality_pairs=87635934
Mon Aug 9 09:44:25 CST 2021: Mapped_unique_quality_valid_pairs=38509955
Mon Aug 9 09:44:25 CST 2021: Intersecting PETs with anchors
Mon Aug 9 09:44:25 CST 2021: Finished the anchor merging.
Mon Aug 9 09:44:25 CST 2021: Finished the anchor processing.
Mon Aug 9 10:02:37 CST 2021: Intrachromosomal_valid_small=2523061
Mon Aug 9 10:03:14 CST 2021: Intrachromosomal_valid_med=8317071
Mon Aug 9 10:03:40 CST 2021: Intrachromosomal_valid_large=8037452
Mon Aug 9 10:03:40 CST 2021: Total number of anchors used: 450
Mon Aug 9 10:03:40 CST 2021: Total number of reads in anchors: 68291
Mon Aug 9 10:04:56 CST 2021: Mapped_unique_intra_quality_anchor=196
Mon Aug 9 10:04:56 CST 2021: Mapped_unique_intra_quality_anchor_small=194
Mon Aug 9 10:04:56 CST 2021: Mapped_unique_intra_quality_anchor_med=1
Mon Aug 9 10:04:56 CST 2021: Mapped_unique_intra_quality_anchor_large=1
Mon Aug 9 10:04:56 CST 2021: Loop_PETs=1
Mon Aug 09 10:04:56 CST 2021: Creating QC report
Mon Aug 09 10:05:03 CST 2021: Creating .rds and .mango files
Mon Aug 09 10:05:14 CST 2021: Deleting temporary files
Mon Aug 09 10:05:14 CST 2021: Done
I paste the tmp file above. Looks like there is something wrong during converting macs2 narrowpeak file to hichipperpeaks
-rw-r--r-- 1 4223284628 Aug 9 23:14 RM01-V1-1.all.Pairs.bed.tmp
-rw-r--r-- 1 10544827638 Aug 9 22:25 RM01-V1-1.all.Pairs.tmp
-rw-r--r-- 1 2372840919 Aug 10 03:42 RM01-V1-1_temporary_control_lambda.bdg
-rw-r--r-- 1 0 Aug 10 05:39 RM01-V1-1_temporary_hichipperPeaks.bed_pad.bed.tmp
-rw-r--r-- 1 76800480 Aug 10 03:44 RM01-V1-1_temporary_peaks.narrowPeak
-rw-r--r-- 1 84741639 Aug 10 03:43 RM01-V1-1_temporary_peaks.xls
-rw-r--r-- 1 56950326 Aug 10 03:45 RM01-V1-1_temporary_summits.bed
-rw-r--r-- 1 4437495159 Aug 10 03:42 RM01-V1-1_temporary_treat_pileup.bdg
-rw-r--r-- 1 3737682486 Aug 9 16:13 RM01-V1-2.all.Pairs.bed.tmp
-rw-r--r-- 1 9326858622 Aug 9 15:30 RM01-V1-2.all.Pairs.tmp
-rw-r--r-- 1 2226846957 Aug 9 20:12 RM01-V1-2_temporary_control_lambda.bdg
-rw-r--r-- 1 0 Aug 10 05:39 RM01-V1-2_temporary_hichipperPeaks.bed_pad.bed.tmp
-rw-r--r-- 1 0 Aug 10 05:47 RM01-V1-2_temporary_peaks.merged.bed.tmp
-rw-r--r-- 1 66143251 Aug 9 20:15 RM01-V1-2_temporary_peaks.narrowPeak
-rw-r--r-- 1 72956604 Aug 9 20:14 RM01-V1-2_temporary_peaks.xls
-rw-r--r-- 1 49012109 Aug 9 20:15 RM01-V1-2_temporary_summits.bed
-rw-r--r-- 1 4037265781 Aug 9 20:12 RM01-V1-2_temporary_treat_pileup.bdg
-rw-r--r-- 1 1671 Aug 10 05:47 V1_loop4.hichipper.log
I also encounter this problem now, can you tell me how to solve it?
I also encounter this problem now, can you tell me how to solve it? Hi Try to skip the background correction procedure by adding the parameter --skip-background-correction Hope U succeed!
Hi, there. I am trying to using hichipper to call loop. In order to call peaks from HiChIP data directly, my yaml looks like under
Then i got an error
Then I check the log file for details
By the way Here is my hichipper command
It is strange that when peaks mode COMBINED,SELF seems work fine, except Loop_PETs=1 ..... And the tests data works well. I got no idea what's going on. Anyone can help? Many thanks.