Mapping data normalizatio
Hi,
I have a question about RNA seq data:
- How much the best standard deviation for the mapping data?
- How can i say my mapping data in RNA seq is normal distribution?
- In normalization of mapping data, what is the mean of the reference (Median Mean, median median,....)?
- In normalization of mapping data, , which methods for RNA seq is the best choice? Scaling or quantile or by totals?
Thank you!
0 answers
No answers yet.
Log in to answer this question.
More posts like this
-
CIBERSORTX disable quantile normalization
written by fifty_fifty •
-
perplexed regarding the process of gene expression normalision
written by DS •
-
Data transformation/normalization/scaling for machine learning using both RNA-Seq and Microarray da…
written by Felipe Colombelli •
-
Is it appropriate to apply quantile normalization on RNA-Seq before computing the Pearson correlati…
written by ATCG
-
Question on targeted quantile-quantile normalization
written by gamma.jian •
-
Normalization methods in RNA-seq read counts data
written by hougiotaejut •
-
How to perform FPKM and TMM calculations?
written by k.kathirvel93
-
Differential expression gene list from TCGA level 3 RNASeq V2 datasets downloaded from UCSC Cancer …
written by zeeniajagga •
-
p values from robust Z scores
written by dharl •
-
Best Method Of Normalization Of Quantitative Traits
written by TJSingh •
Standard deviation for what? The insert size? Nothing even uses that any more (don't waste your time with inferior tools like CLC when you can use better platforms for free).