Hi,
I have an input, that can be fasta,fastqsanger,fastqillumina:
I have multiple outputfiles - bundled in a list collection:
The format_source parameter doesn't work - the files in the list (extension
fq) are of format "fq"
How can I make it possible that they are fasta,fastqsanger
Hi all - It looks like bowtie's wrapper is working incorrectly for a list
of dataset pairs. Its expecting all the forward reads in one dataset list
and the reverse reads in a separate dataset list.
Instead, I have a list of dataset pairs (for paired-end data). This cannot
be provided to bowtie a
hmm, no replies yet, so is anybody able to reproduce this behavior and
would you not consider it a bug?
Best,
Wolfgang
On 06/16/2015 03:11 PM, Wolfgang Maier wrote:
Dear all,
with older Galaxies (prior to latest_15.03 I think), you could satisfy
Galaxy's samtools dependence for indexing bam
