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control file = ['WT_INPUT_REP1.mLb.clN.sorted.bam']
effective genome size = 1.00e+06
band width = 300
model fold = [5, 50]
qvalue cutoff for narrow/strong regions = 5.00e-02
qvalue cutoff for broad/weak regions = 1.00e-01
The maximum gap between significant sites is assigned as the read length/tag size.
The minimum length of peaks is assigned as the predicted fragment length "d".
Larger dataset will be scaled towards smaller dataset.
Range for calculating regional lambda is: 1000 bps and 10000 bps
Broad region calling is on
Paired-End mode is off
INFO @ Thu, 14 Dec 2023 23:22:41: #1 read tag files...
INFO @ Thu, 14 Dec 2023 23:22:41: #1 read treatment tags...
INFO @ Thu, 14 Dec 2023 23:22:43: 1000000
INFO @ Thu, 14 Dec 2023 23:22:44: 1702472 reads have been read.
INFO @ Thu, 14 Dec 2023 23:22:44: #1.2 read input tags...
INFO @ Thu, 14 Dec 2023 23:22:45: 1000000
INFO @ Thu, 14 Dec 2023 23:22:46: 1729564 reads have been read.
INFO @ Thu, 14 Dec 2023 23:22:46: #1 tag size is determined as 40 bps
INFO @ Thu, 14 Dec 2023 23:22:46: #1 tag size = 40.0
INFO @ Thu, 14 Dec 2023 23:22:46: #1 total tags in treatment: 1702472
INFO @ Thu, 14 Dec 2023 23:22:46: #1 total tags in control: 1729564
INFO @ Thu, 14 Dec 2023 23:22:46: #1 finished!
INFO @ Thu, 14 Dec 2023 23:22:46: #2 Build Peak Model...
INFO @ Thu, 14 Dec 2023 23:22:46: #2 looking for paired plus/minus strand peaks...
INFO @ Thu, 14 Dec 2023 23:22:46: #2 number of paired peaks: 0
WARNING @ Thu, 14 Dec 2023 23:22:46: Too few paired peaks (0) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead.
WARNING @ Thu, 14 Dec 2023 23:22:46: Process for pairing-model is terminated!
I believe this might be an issue because I am using a bacterial genome and other users on the MACS2 GitHub have reported similar problems (macs3-project/MACS#390).
I was wondering what is the best way to resolve this issue? Thanks!
Command used and terminal output
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Relevant files
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System information
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The text was updated successfully, but these errors were encountered:
Sorry for the late response, probably not useful to you anymore but in case someone in the future finds this issue, you could provide the --nomodel and --extsize 147 arguments to macs2 as suggested in the tool message. See this answer in nf-core slack.
Description of the bug
Hello,
While running the pipeline, it is encountering issues when running MACS2. Here are the specifics:
-[nf-core/chipseq] Pipeline completed with errors-
ERROR ~ Error executing process > 'NFCORE_CHIPSEQ:CHIPSEQ:MACS2_CALLPEAK (WT_HRCA_IP_REP1)'
Caused by:
Process
NFCORE_CHIPSEQ:CHIPSEQ:MACS2_CALLPEAK (WT_HRCA_IP_REP1)
terminated with an error exit status (1)Command executed:
macs2
callpeak
--keep-dup all --broad --broad-cutoff 0.1
--gsize 1000000
--format BAM
--name WT_HRCA_IP_REP1
--treatment WT_HRCA_IP_REP1.mLb.clN.sorted.bam
--control WT_INPUT_REP1.mLb.clN.sorted.bam
cat <<-END_VERSIONS > versions.yml
"NFCORE_CHIPSEQ:CHIPSEQ:MACS2_CALLPEAK":
macs2: $(macs2 --version | sed -e "s/macs2 //g")
END_VERSIONS
Command exit status:
1
Command output:
(empty)
Command error:
INFO @ Thu, 14 Dec 2023 23:22:41:
Command line: callpeak --keep-dup all --broad --broad-cutoff 0.1 --gsize 1000000 --format BAM --name WT_HRCA_IP_REP1 --treatment WT_HRCA_IP_REP1.mLb.clN.sorted.bam --control WT_INPUT_REP1.mLb.clN.sorted.bam
ARGUMENTS LIST:
name = WT_HRCA_IP_REP1
format = BAM
ChIP-seq file = ['WT_HRCA_IP_REP1.mLb.clN.sorted.bam']
control file = ['WT_INPUT_REP1.mLb.clN.sorted.bam']
effective genome size = 1.00e+06
band width = 300
model fold = [5, 50]
qvalue cutoff for narrow/strong regions = 5.00e-02
qvalue cutoff for broad/weak regions = 1.00e-01
The maximum gap between significant sites is assigned as the read length/tag size.
The minimum length of peaks is assigned as the predicted fragment length "d".
Larger dataset will be scaled towards smaller dataset.
Range for calculating regional lambda is: 1000 bps and 10000 bps
Broad region calling is on
Paired-End mode is off
INFO @ Thu, 14 Dec 2023 23:22:41: #1 read tag files...
INFO @ Thu, 14 Dec 2023 23:22:41: #1 read treatment tags...
INFO @ Thu, 14 Dec 2023 23:22:43: 1000000
INFO @ Thu, 14 Dec 2023 23:22:44: 1702472 reads have been read.
INFO @ Thu, 14 Dec 2023 23:22:44: #1.2 read input tags...
INFO @ Thu, 14 Dec 2023 23:22:45: 1000000
INFO @ Thu, 14 Dec 2023 23:22:46: 1729564 reads have been read.
INFO @ Thu, 14 Dec 2023 23:22:46: #1 tag size is determined as 40 bps
INFO @ Thu, 14 Dec 2023 23:22:46: #1 tag size = 40.0
INFO @ Thu, 14 Dec 2023 23:22:46: #1 total tags in treatment: 1702472
INFO @ Thu, 14 Dec 2023 23:22:46: #1 total tags in control: 1729564
INFO @ Thu, 14 Dec 2023 23:22:46: #1 finished!
INFO @ Thu, 14 Dec 2023 23:22:46: #2 Build Peak Model...
INFO @ Thu, 14 Dec 2023 23:22:46: #2 looking for paired plus/minus strand peaks...
INFO @ Thu, 14 Dec 2023 23:22:46: #2 number of paired peaks: 0
WARNING @ Thu, 14 Dec 2023 23:22:46: Too few paired peaks (0) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead.
WARNING @ Thu, 14 Dec 2023 23:22:46: Process for pairing-model is terminated!
I believe this might be an issue because I am using a bacterial genome and other users on the MACS2 GitHub have reported similar problems (macs3-project/MACS#390).
I was wondering what is the best way to resolve this issue? Thanks!
Command used and terminal output
No response
Relevant files
No response
System information
No response
The text was updated successfully, but these errors were encountered: