The R package exomePeak2 is nice and ideal for m6A-Seq analysis in our group.
But recently a result troubled me:
In the Differential Modification Analysis result: DiffMod.xlsx, the padj column have many NA. And the corresponding pvalue rank from 0.00000135 to 0.999901024.
I dont konw how to deal with these peaks, can you help offer some help?
And a minor question:
What does the DiffModLog2FC mean, it seems derived from "ModLog2FC_treated-ModLog2FC_control" or like log2(IP.Treated/IP.Control) ?
And in your group, waht's the better parameter cutoff for Differential Modification Peaks? pvalue or padj 0.05, and should a cutoff on DiffModLog2FC?
Thank you in advance for your reply!
Haifeng Sun
Nanjing Medical University, Jiangsu Province
The supplementary materials was emailed to you (Zhen.Wei01@xjtlu.edu.cn).
Hi, ZhenWei:
The R package exomePeak2 is nice and ideal for m6A-Seq analysis in our group.
But recently a result troubled me:
In the Differential Modification Analysis result: DiffMod.xlsx, the padj column have many NA. And the corresponding pvalue rank from 0.00000135 to 0.999901024.
I dont konw how to deal with these peaks, can you help offer some help?
And a minor question:
What does the DiffModLog2FC mean, it seems derived from "ModLog2FC_treated-ModLog2FC_control" or like log2(IP.Treated/IP.Control) ?
And in your group, waht's the better parameter cutoff for Differential Modification Peaks? pvalue or padj 0.05, and should a cutoff on DiffModLog2FC?
Thank you in advance for your reply!
Haifeng Sun Nanjing Medical University, Jiangsu Province
The supplementary materials was emailed to you (Zhen.Wei01@xjtlu.edu.cn).
Thanks again!