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When running smrnaseq with technical repeats I get the error:
Process `NFCORE_SMRNASEQ:SMRNASEQ:MIRNA_QUANT:MIRTOP_QUANT` input file name collision -- There are multiple input files for each of the following file names:
To run the pipeline I used this command:
nextflow run nf-core/smrnaseq \
--outdir './nfcore' \
--input './samplesheet.csv' \
--genome GRCh38 \
--protocol qiaseq \
-profile crick \
-r 2.1.0
The samplesheet.csv file has three columns, sample, fastq_1, and fastq_2. There are duplicated entries in the sample column, as some samples were sequenced over multiple runs.
Please could a concatenate step be added to merge technical repeats?
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