SingleCell RNaseq normalisation
Hi I am analysing singleCell RNAseq data, in one batch of cells I have more spike-in than in the others (a different concentration of spike_in has been added to the RNA). I was wondering what is the best procedure to normalise the data to be able to integrete these cells in the analysis Thank you Nadia
• 1,315 views
•
link
written
by
nadia_boufaied •
0 answers
No answers yet.
Log in to answer this question.
More posts like this
-
How to normalise the RNAseq data without spike in?
written by Mo •
-
Normalization of RNA-Seq Counts with ERCC spike-ins
written by Berta •
-
Problems with QIAseq spike-in normalization
written by lluc.cabus •
-
Normalisation of RNA-seq data for coexpression analysis
written by DanTzo •
-
what does the alignment statistics of your RNA spike-in tell you about your sample of interest in t…
written by Zee_S
-
ERCC spike-ins in RNA-Seq data.
written by Victoria •
-
RNASeq TCGA data
written by elizabethR
-
read count normalization for spike
written by Sara
-
DIY RNA Spike-in controls for qRTPCR
written by samantha_jeschonek
-
Comparisons between datasets generated at different timepoints
written by l.lavitas •
