All,
It is noticed that Galaxy/GATK indexes reference fasta dbSNP file everytime
when it runs. Re-indexing takes time (~10min), hence it affects overall run
time when it use for multiple times. However, this could be avoided by reusing
the available index. Here is the snapshot of the log:
Hi,
I´m using Galaxy (main) browser on a Win 7 PC to get statistics from my
sequencing runs. Now I have bam files which are too big for upload from my
local hard drive so I tried to ftp upload to main.g2.bx.psu.edu via a client
(FileZilla). The transfer of files seems to be complete but the
Hello Lindsey,
Yes, you have this correct. The general path would be to:
- join forward and reverse data per run
- run FASTQ Groomer FastQC
(note: if your data is already in Sanger FASTQ format with Phred+33
quality scaled
values, the datatype '.fastqsanger' can be directly assigned
Helllo Hans,
Some items to double check:
1 - The ftp server is: main.g2.bx.psu.edu
2 - Files are 50G or smaller. This is a hard limit - if your data is
larger, a local or cloud instance will be needed: http://getgalaxy.org
3 - FileZilla reports that FTP is successful (there is a tab at the
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