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Hi all, new to next flow here. Two related questions:
I want the following in my config file:
process {
publishDir {
path = '.'
mode = 'link'
enabled = { task.ext.publish }
}
}So that I can turn on publication in my processes by just setting task.ext.publish to true or false, depending. (This way I don't have to respecify the path or link each time)
However, there are two issues: in the config file, it seems that task.ext.publish is interpreted as process.publishDir.task.ext.publish which isn't what I want. Also, I can't seem to set ext.publish from my process, the period in ext.publish true seems to be screwing things up.
Any advice? Thanks!
Hi! When I try to run nf-core on my local PC after a long time, I get the following error. Does anyone know the cause?
nextflow run nf-core/rnaseq -profile test,docker -r 3.3
N E X T F L O W ~ version 21.09.1-edge
Launching `nf-core/rnaseq` [disturbed_meucci] - revision: 8094c42add [3.3]
ERROR: Validation of pipeline parameters failed!
* --hostnames: expected type: String, found: JSONObject ({"cfc":[".hpc.uni-tuebingen.de"],"utd_sysbio":["sysbio.utdallas.edu"],"utd_ganymede":["ganymede.utdallas.edu"],"genouest":[".genouest.org"],"cbe":[".cbe.vbc.ac.at"],"genotoul":[".genologin1.toulouse.inra.fr",".genologin2.toulouse.inra.fr"],"crick":[".thecrick.org"],"uppmax":[".uppmax.uu.se"],"icr_davros":[".davros.compute.estate"],"imperial":[".hpc.ic.ac.uk"],"binac":[".binac.uni-tuebingen.de"],"imperial_mb":[".hpc.ic.ac.uk"]})I could not figure out how to uninstall Nextflow. So I simply ran the following command one more time.
curl -s https://get.nextflow.io | bash Then I moved the created nextflow file to the path. Now it works properly.
Is it possible for me to access the params such that I can write them as an output? In my particular workflow, several of the params used are things like "password needed to unzip file", which I'd like to save for posterity in the output location. I'm basically trying to do:
params_json = new JsonBuilder(params).toString()
process xxx {
shell:
'''echo !{params_json} > params.json'''
}But it's not letting me. Is there some other nice way for me to do this?
9 replies
+([0-9]). How do you all deal with this?Channel.fromFilePairs(["*_S[0-9]_L00[1-9]_{R1,R2}_001.fastq.gz",
"*_S[0-9][0-9]_L00[1-9]_{R1,R2}_001.fastq.gz",
"*_S[0-9][0-9][0-9]_L00[1-9]_{R1,R2}_001.fastq.gz",
"*_S[0-9][0-9][0-9][0-9]_L00[1-9]_{R1,R2}_001.fastq.gz"]).set { illumina_q }
Hey all. I have trouble cat two files together under shell. Outside of nextflow run, everything work flawlessly.
shell:
'''
echo "read1: NA12878_S1_L001_R1_001.fastq.gz NA12878_S1_L002_R1_001.fastq.gz"
echo "read2: NA12878_S1_L001_R2_001.fastq.gz NA12878_S1_L002_R2_001.fastq.gz"
echo $(ls)
cat NA12878_S1_L001_R1_001.fastq.gz NA12878_S1_L002_R1_001.fastq.gz > read1.fastq.gz
cat NA12878_S1_L001_R2_001.fastq.gz NA12878_S1_L002_R2_001.fastq.gz > read2.fastq.gz
'''
Command exit status:
1
Command output:
read1: NA12878_S1_L001_R1_001.fastq.gz NA12878_S1_L002_R1_001.fastq.gz
read2: NA12878_S1_L001_R2_001.fastq.gz NA12878_S1_L002_R2_001.fastq.gz
NA12878_S1_L001_R1_001.fastq.gz NA12878_S1_L001_R2_001.fastq.gz NA12878_S1_L002_R1_001.fastq.gz NA12878_S1_L002_R2_001.fastq.gz
Command error:
cat: NA12878_S1_L001_R1_001.fastq.gz: No such file or directory
cat: NA12878_S1_L002_R1_001.fastq.gz: No such file or directory
13 replies
Hi all, How much does it cost to run a workflow using tower and aws-batch + fsx lustre? I'm working on a customer project right now and want to evaluate this option. Perhaps some guidance to the documentation and pricing model is needed.
Using aws-batch mode with s3 only work directory is not very efficient.
What is the commercial license price
Hi all, I'm looking for a method to convert paired end data from bcl2fastq process output into fastq file pair tuple. @happykhan's method is the only I found. Is there some more elegant way with DSL2? Currently I have a standard bcl2fastq process that emits
*.fastq.gzand I can read in the sample sheet, but I'd need to match sample sheet names and filename. Is there some way to use something like the.fromFilePairs factory on an existing channel?
nextflow.enable.dsl=2
process createFiles {
output:
path("*.txt", emit: apath)
script:
"""
#!/usr/bin/env python
filenames = ['a.txt', 'b.txt', 'c.txt']
for f in filenames:
with open(f, "w") as wf:
wf.write("hello\\n")
print(f)
"""
}
process printContent {
input:
path(x)
script:
"""
cat $x
"""
}
workflow {
createFiles()
printContent(createFiles.out.apath)
}executor > local (2)
[67/0c496d] process > createFiles [100%] 1 of 1 ✔
[1b/36a13c] process > printContent [100%] 1 of 1 ✔
workflow {
createFiles()
printContent(createFiles.out.apath.flatten())
}
Is it possible to create files with the native execution mode of a process? For example, I attempted the following:
process WRITE_FASTP_METRICS{
input:
val (rna_result)
val (adt_result)
output:
path "fastp_metrics.csv"
exec:
write_out = file("fastp_metrics.csv")
rna_result.forEach{key, value ->
write_out << key << ',' << value << '\n'
}
adt_result.forEach{key, value ->
write_out << key << ',' << value << '\n'
}
}But the fastp_metrics.csv is not created in the work directory, causing this error: Missing output file(s) ``fastp_metrics.csv`` expected by process ``WRITE_FASTP_METRICS (1)``
i'm wondering if we can pass in a container as a variable, as i want to test the same process over various versions of a software. something like this:
process A {
container= container_label
input:
tuple val(container_label), path(inputFile)
...
}this code did not work, however. can it be done in another way?
process A {
container= params.container_label
input:
path(inputFile)
...
}process A {
input:
tuple val(container_label), path(inputFile)
...
script:
task.container = container_label
...
}
Does anyone know if there will be any nextflow workshop in the near future? I see that there was one in July of 2020 and another one in May of this year hosted by ecseq and was wondering if anyone knows if a similar event will be taking place in the future.
2 replies
5 replies
process generate_readset {
tag "$sample_id"
cpus 48
input:
tuple val(read_name), val(chromosome1), val(chromosome2), val(cuteSV_pos1), val(cuteSV_pos2),
val(sniffle_pos1), val(sniffle_pos2),
path(cuteSV_vcf), path(sniffles_vcf) from vcf_input
output:
path 'complete_read_set.txt' into receiver
script:
"""
${bcftools_1_11} view --threads ${task.cpus} $cuteSV_vcf -r chr$chromosome1:$cuteSV_pos1-$cuteSV_pos2 > complete.txt
"""}
Remote resource not found: https://api.github.com/repos/PATH/TO/contents/main.nf. What am I doing wrong?