/home/local/bin/Rscript ./defuse-0.6.1//scripts/evaluate_fraglength_mean.R
This is your problem, I believe. The double forward slash betweeen defuse-0.6.1 and scripts.
Check your config.txt file to make sure you named your directories without a slash at the end. ie:
/home/usr/defuse-0.6.1
NOT:
/home/usr/defuse-0.6.1/
Unconfigured Ad
Collapse
X
-
Defuse Calculating spanning p-values Failure
Hey, could anyone help me with one problem:
when I run defuse to find gene fusions based on fastq data (illumina HISEQ, paired-end, trimed by trimglore), the software goes well until Calculating spanning p-values:
Importing fastq files
Splitting fastq files
Discordant alignments
Read Stats
Fragment mean 182.171678030117 stddev 43.6861609169054
Read length min 20 max 100
Generating discordant alignment clusters
Remove mitochondrial-genomic clusters
Generating maximum parsimony solution
Selecting fusion clusters
Preparing sequences for local realignment
Performing local realignment
Filtering concordant clusters
Generating spanning alignment regions file
Initializing split read alignments
Calculating split read alignments
Evaluating split reads
Calculating spanning stats
Calculating spanning p-values
Failure for defuse command:
/home/local/bin/Rscript ./defuse-0.6.1//scripts/evaluate_fraglength_mean.R ./temp/defuse/concordant.read.stats ./temp/defuse/spanlength.cov 50 ./temp/defuse/splitreads.span.stats ./temp/defuse/splitreads.span.pval.tmp
Reason:
Job command with nonzero return code
Job output:
Running on node4
Rscript execution error: No such file or directory
real 0m0.099s
user 0m0.000s
sys 0m0.003s
Return codes: 255
Commands failed after 1 seconds
when I check I found there is no ./temp/defuse/splitreads.span.pval.tmp produced, what is the reason?
thanks in advance for anyone's reply.
code as bellow:
~/programs/defuse-0.6.1/scripts/defuse.pl -c ~/programs/defuse-0.6.1/scripts/config.txt -1 $inputdir/$file1 -2 $inputdir/$file2 -o $outputdir -p 24Tags: None
-
Latest Articles
Collapse
-
by SEQadmin2
Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.
The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
...-
Channel: Articles
06-02-2026, 10:05 AM -
-
by SEQadmin2
With the launch of new single-cell sequencing platforms in 2026, the field stands at an exciting inflection point. This article surveys the most impactful advances in the field and discusses how they’re reshaping research in cancer, immunology, and beyond.
Introduction
Single-cell sequencing technologies have undergone remarkable advances over the past decade, transitioning from low-throughput experimental approaches to highly scalable platforms capable of...-
Channel: Articles
05-22-2026, 06:42 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, 06-05-2026, 10:09 AM
|
0 responses
11 views
0 reactions
|
Last Post
by SEQadmin2
06-05-2026, 10:09 AM
|
||
|
Started by SEQadmin2, 06-04-2026, 08:59 AM
|
0 responses
23 views
0 reactions
|
Last Post
by SEQadmin2
06-04-2026, 08:59 AM
|
||
|
Started by SEQadmin2, 06-02-2026, 12:03 PM
|
0 responses
28 views
0 reactions
|
Last Post
by SEQadmin2
06-02-2026, 12:03 PM
|
||
|
Started by SEQadmin2, 06-02-2026, 11:40 AM
|
0 responses
22 views
0 reactions
|
Last Post
by SEQadmin2
06-02-2026, 11:40 AM
|
Leave a comment: