Closed yaaminiv closed 5 years ago
I'd assume this would be the goal of unite
in methylKit
, but I haven't figured out why it's not giving us the output we want (yet).
.cov files have methylation for each loci, as well as coverage.
Limit to 5x then you can call each loci. On Mar 17, 2019, 4:14 PM -0700, Yaamini Venkataraman notifications@github.com, wrote:
I'd assume this would be the goal of unite in methylKit, but I haven't figured out why it's not giving us the output we want (yet). — You are receiving this because you are subscribed to this thread. Reply to this email directly, view it on GitHub, or mute the thread.
To clarify: I plan on just looking at the 5 samples from the control to not induce treatment effects. Is this the correct approach?
That is fine… On Mar 18, 2019, 9:04 AM -0700, Yaamini Venkataraman notifications@github.com, wrote:
To clarify: I plan on just looking at the 5 samples from the control to not induce treatment effects. Is this the correct approach? — You are receiving this because you commented. Reply to this email directly, view it on GitHub, or mute the thread.
I want to describe general methylation trends, irrespective of pCO2 treatment in my C. virginica gonad data. Claire and Mac both had sections in their papers where determined if a CpG locus was methylated or not. From Mac's 2013 PeerJ paper:
I believe this was done
methratio
in BSMAP (Claire's notebook). Is there a way to do this withbismark
ormethylKit
?