Hi,
I am trying to look mutations/SNPs in RNA-Seq data. Can anyone suggest me a
workflow in Galaxy on how to detect SNPs and mutations
Thanks in advance
Suz
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Hello,
I am new to using Galaxy tools. I am running paired end RNA-Seq data on
Galaxy and I want to differential gene expression between control and
treated samples
I was fine until running TopHat output, I am having problems with cufflinks
and cuffdiff output.
I ran the cufflinks and cuffdiff
Hello everyone,
I am trying to upload files (size:6GB) via ftp and i am using FileZilla for
ftp upload of files.
Host/usernames and password details as follows:
Host: main.g2.bx.psu.edu
Username: My galaxy Username
Password: Galaxy password
I found this tutorial for FTP upload.
Hello,
I am trying to do RNAseq analysis on Paired end data Illumina. I have about
4 files for each sample (2 forward and 2 reverse).
I want to analyze the data in Galaxy.
Do I have to groom and run the QC for each file? Should I join the paired
files and run both tools on each pair, or should
Hello,
I am trying to run TopHat for paired end and this is my first time using
Galaxy and TopHat and I have a doubt regarding what to mention in Mean
Inner Distance between Mate Pairs:The default value is 20.
Should I leave the value or should I be changing the value.
What is Mean Inner
Hello,
Is there any plan of installing TopHat fusion in Galaxy in near future.
Thanks
Katie
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