I am trying to use the galaxy "BED to GFF" function.  The operation worked,
but instead of giving me back any feature information (e.g., exon, intron,
repeat, etc.); I just received back the sequence of the interval contained
within the BED file.  Does anyone know what I'm doing wrong?  Moreover, does
anyone know the best way to map each read of a RNAseq run to a given
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