Hi, I did differential expression by DEseq2 for some coding and lncoding RNAseq data,this is my summery result of DEseq2 by adjusted p-value < 0.1:
for lncoding:
out of 26998 with nonzero total read count
adjusted p-value < 0.1
LFC > 0 (up) : 10, 0.037%
LFC < 0 (down) : 13, 0.048%
outliers [1] : 241, 0.89%
low counts [2] : 11375, 42%
(mean count < 1)
and for coding:
out of 19933 with nonzero total read count
adjusted p-value < 0.1
LFC > 0 (up) : 335, 1.7%
LFC < 0 (down) : 300, 1.5%
outliers [1] : 289, 1.4%
low counts [2] : 6012, 30%
(mean count < 61)
as you see I have 23 genes for lncoding ad 635 genes for coding after filtering,this number of genes is OK for making co-expression network?
1 answer
You can draw a co-expression network with just two genes. If you do not set a correlation threshold, you will have a network with 2 nodes and 1 edge.
Since you have 658 genes, which will give you a maximum of around 200k edges, you can try out different thresholds to decrease the number of edges. I suggest that you should try out different thresholds to see if your network is fine. Whether it is OK or not depends on your data and your experiment.
I hope this helps.
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