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
Hi
I have a few questions
1. I am trying to use Bowtie to map my data using a reference genome.
the genome is available on Galaxy (Escherichia coli DH10B (20079)). Is
there a way that I can download the file in fasta format to use as a
reference in Tablet?
I can import the SAM output into Tablet
Hi
Is there an stand alone ( ie not a component of Bowtie etc ) program
in galaxy that can filter or trim fastq data?
thanks
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