Hi everyone,
I’m trying to run nf-core/sopa on my MACSima imaging samples.
I’m working on a RedHat HPCC environment, using:
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Nextflow version: 25.10.0
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nf-core/sopa revision: master (commit 11b4cccb7e)
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Container engine: Singularity
My config.yml
# For parameters details, see this commented example: https://github.com/gustaveroussy/sopa/blob/df30da607cea4326d7ea907dbec86cb2bca078b3/workflow/config/example_commented.yaml
read:
technology: macsima
patchify:
patch_width_pixel: 3000
patch_overlap_pixel: 40
segmentation:
cellpose:
diameter: 35
channels: [ "DAPI" ]
flow_threshold: 2
cellprob_threshold: -6
min_area: 400
aggregate:
aggregate_channels: true
min_intensity_ratio: 0.1
expand_radius_ratio: 0.1
explorer:
ram_threshold_gb: 4
pixel_size: 0.170
My samplesheet.csv
sample,data_path
ROI1,/storage/scratch01/groups/lc/rnafusion_pdx/sopa/sample1/
ROI2,/storage/scratch01/groups/lc/rnafusion_pdx/sopa/sample2/
The directory contains the MACSima output (multiple TIFFs).
Command used
/home/jgracia/bin/nextflow run nf-core/sopa -profile singularity --input samplesheet.csv -params-file config.yml --outdir /storage/scratch01/groups/lc/rnafusion_pdx/sopa/ --email josearacena111@gmail.com
The problem
ERROR ~ Validation of pipeline parameters failed!
Entry 1: Missing required field(s): fastq_1
Entry 2: Missing required field(s): fastq_1
Even though I explicitly set:
read:
technology: macsima
This doesn’t make much sense since MACSima doesn’t produce reads of any kind, and since the tecnology used is specified I’m not sure how to solve the error.