Hi Galaxy Users,
I'm very new to galaxy and have read/watched MANY galaxy tutorials but I have
some questions for other users out there:
What are the top 10 ways that you find most useful for your analysis,
especially to those who work with whole genome sequencing data?
Thanks for your help
Dear Galaxy Users,
I had a quick question as a new Galaxy user. I just received WGS data from
Illumina where I'm given .bam files. I am not given .fastq files. Most of the
Galaxy tutorials I've seen online have started with raw data in .fastq format.
Can Galaxy handle if I were to upload a
things are moving almost instantaneously.
Thanks for your insight!
Best,
Priya
From: Jennifer Jackson [j...@bx.psu.edu]
Sent: Tuesday, March 26, 2013 12:14 PM
To: Priya Bhatt
Cc: galaxy-user@lists.bx.psu.edu
Subject: Re: [galaxy-user] History items remain
Dear Galaxy Users,
Forgive me in advance, but I am a VERY new Galaxy user!
I am trying to go through the Galaxy 101 tutorial provided on the galaxy
website (https://main.g2.bx.psu.edu/u/aun1/p/galaxy101). The first step asks
to get exon data of Chromosome 22 from UCSC database, and the second
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