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rensanhao
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@rensanhao-21464
Last seen 5.5 years ago
Hi,
I created two the tximport object (untreated vs treated) from salmon,which is a S4 object has four cols name as abundance, counts, length, and countsfromabundance.My question is how to merge these two dataset into one so I could import them with using DESeqDataSetFromTximport?
Thanks.
Thanks for this quick reply. So following this merged dataset, how to label which group is my control group or treated group? or should I add a column to label the salmon-quant.sf files before this integration?
Add it in the dds construction step (eg DESeqDataSetFromTximport) as colData.
I'm sorry but I didn't get it. According to vignette,I think the code
is essential for labeling the group info, but I didn't fully understand how it works and moreover, it also led me to confuse that
the design arguments should also work for specifying the group information? I just started learning R and RNA-seq so I'll very appreciate if you feel necessary to explain some basic knowledge regarding this issue.
Thanks a lot.
Maybe you can partner with a person who has experience with R. On the support site I try to assist users who have questions about the software, but you probably need to have some R background to get started. You want to have a table of sample information so that you can import all the samples at once with one call to tximport().
Thanks. I have some clues about this now.
Thanks for this quick reply. So following this merged dataset, how to label which group is my control group or treated group? or should I add a column to label the salmon-quant.sf files before this integration?