batch correction
Hey Guys,
Please let me know how to perform batch corrections of scRNA seq data when the data is recorded at different time points.
Please suggest.
Thanks in advance.
single
cell
• 756 views
•
link
updated
by
LauferVA
•
written
by
shiviagarwalpharma •
0 answers
No answers yet.
Log in to answer this question.
More posts like this
-
Expression data of diabetic patients
written by shiviagarwalpharma •Hi Guys, Can you please let me know that what are the resources to download RNA Seq expression data of diabetic patients. Thanks in advance
-
batch correction of single cell dataset
written by shiviagarwalpharma •Hi, I have single cell datasets recorded at different time points. I have to concatenate them and analyse as a single dataset. But I am …
-
Annotate clusters
written by shiviagarwalpharma •Hey Guys, Is there any way to annotate (Pathway/Disease/Function/Ontology) different clusters (module) obtained after single cell analysis using Seurat or any other package ? Please …
-
PATHWAY
written by shiviagarwalpharma •Hi Guys, Can you suggest a good alternative of IPA software for pathway analysis? Thanks in advance
-
integrated scRNA-seq dataset
written by tomas4482 •I read a lot of methods about integration of multiple scRNA-seq datasets from different cohorts, species, or experimental designs. I'm curious about a question. It …
-
batch correction in ChIp-seq data
written by BogdanDear all, when working with a set of ChIP-seq data that is collected at multiple time points, which algorithm would you use (if any) for …
-
about the batch correction and integration and normalization of scRNA-seq data
written by BogdanDear all, i would appreciate your opinions, comments, advises on the following please : <> we do have a two batches of scRNA-seq in CTRL …
-
Batch effect correction
written by gstavropoulos1991 •Dear all, I want to correct for batch effects. I have two data sets, two similar diseases, measured at completely different time points. When I …
-
single cell RNA-seq 10X genomics
written by rob.costa1234I am getting some single cell RNA-seq data for different time points. Is there a standard work flow reported for such analysis? I know there …
-
Advice required for remove batch effect which perfectly collinear with contrast of interest
written by boymin2020 •I have merged two RNA-seq datasets from two different batches. The problem is that the sequencing batches are perfectly collinear now with cell type, which …
you are unlikely to get substantive responses to this post for a couple reasons.
1) its a fairly technically complex process
2) the reader cant understand what level of knowledge you possess, or what you have tried yet on your own
3) there is a LOT written about this already in the published literature, as well as on website like Seurat3 or 4 or 8 or whatever version they are on
my suggestion would be that you start reading papers about cell cycle scoring and regression, which you will probably need to read about and perform anyway.
while you dont describe what is happening in your cells between time points, possibly the mathematics used for CCS/CCR are similar and you can go from there?
otherwise write a more detailed question and go from there.