bgruening / galaxytools

:microscope::books: Galaxy Tool wrappers
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Salmon doesn't work correctly with paired-end reads #1260

Closed gallardoalba closed 1 year ago

gallardoalba commented 1 year ago

When providing a collection of paired-end read as input, Salmon works in that way:

salmon quant --index './index' --libType A --unmatedReads <(zcat < ./single.fastq) "

However, it should work as follow:

salmon quant -i transcripts_index -l <LIBTYPE> -1 reads1.fq -2 reads2.fq