Figure for relative error with large database
I have some data of RNAs in different tissues, and I worked out the relative errors of my data and the data provided by the reference. I want to describe the range of the relative error to know that whether I did the pipeline correctly or not. Could someone give me some advice to do that? Python or R will be better.
Here is the structure of the reference data, there are some scores of each gene in different tissues. My data and the relative error have the same structure. BTW, I have thousands of gene.
GeneID Adrenal.gland Cerebellum Brain Fetal.brain Fetal.liver
ENSG00000000419
ENSG00000000457
ENSG00000000460
ENSG00000000938
ENSG00000000971
0 answers
No answers yet.
Log in to answer this question.
More posts like this
-
Unable to load scRNAseq data into R with Read10X
written by Rogerio Ribeiro •
-
Converting Ensembl gene id to Gene symbol
written by Zahra •
-
Loading PCA - different value depending on the package used
written by camillab. •
-
Figure for relative error with large database
written by Evy_00 •
-
NOISeq Fold Change calculation seems off?
written by VBer
-
Singe cell identification library with Ensembl_ID:s
written by chilifan
-
loading data file into GSEA
written by ashkan
-
Check if RNASeq count data follow NB or Poisson distributions
written by debitboro
-
mapping ensembl gene id to an array id
written by yasjas •
-
How To Calculate The Rpkm For The Count Tables Of Rna Seq Data
written by narges •
