Hi, I have an Illumina HiSeq lane of sequences, in which I input multiple
samples with 5-prime 6 bp barcodes. The barcodes were added in a way so that
the barcodes are the first 6 bp in the reads. What I need to do is to sort
my reads according to the barcodes, then clip off the barcodes and use
Hello!
I tried asking this at the galaxy-dev list a while back, but figure it
might more rightly belong on this list.
I am trying to configure the Gencode Partition tool on our local
installation of Galaxy. However, I am not able to find any information
about what sort of files it should
Hi
We have installed Galaxy on a local machine (Mac pro 2 x 2.4 gHz quad
core Intel Xeon with 32 GB RAM). We wish to use dynamic trimmer in
order to trim the data and while downloading a groomed file from
galaxy, it runs out of memory.
Please advise.
Sent from my iPhone
3 matches
Mail list logo