Hello,
Making the assumption that your data is DNA (and not RNA), the tools
under "NGS: SAM Tools" and "Operate on Genomic Intervals" can generate
coordinates of the mapped reads which then can be correlated with known
genes/ORFs from your bacterial genome (or related genomes, if you can
obta
Hi
I am sequencing a bacterial genome and have assembled my Illumina
reads (40 bp single) using bowtie with a reference genome. This
generated a sam file.
I would like to obtain a listing of the open reading frames from the
bacterial genome and the corresponding genes that they are most
similar to.
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