I have a DE matrix of Single cell RNAseq data for two conditions. there are 500 genes that has FDRp<0.01, FC>2. I want to reduce the list to say around 100-200 genes to make it more presentable. Is there any stringency criteria that I can use for SCRNAseq data, like sequencing depth, read counts? what is commonly used for such purposes in ScRNAseq data.