Hello,

I am working on single cell RNA seq analysis wanted to normalize my read count which are coming from HTseq, working on different methods of normalization such as TMM(edgeR), RLE(DEseq2), scran, SCnorm, linnorm, quantile normalization how to choose which one is better, and also how I can show better way of visualization that my normalization worked well if any one suggest me more information regarding any visualization strategy will be better with some explanation

Thank you