Open ZhijieHanbioinfor opened 1 month ago
Dear user,
Thank you for your interest in our methods.
We have not tested if microarray data can be used as reference. We noted one recent study that applied BayesPrism to deconovovle the microarray bulk (https://www.biorxiv.org/content/10.1101/2023.06.14.544991v1.full), which seems to perform well. You may give it a try and see if the results make sense.
You may also try using markers when constructing the scRNA-seq reference to overcome the strong technical difference between RNA-seq and microarray data to see if it improves the results (provided you have some prior knowledge about the ground truth).
Best,
Tinyi
Hi Zhijie,
Thank you for your questions. Please refer to this reply: https://github.com/Danko-Lab/BayesPrism/issues/56#issuecomment-1669620258
Best,
Tinyi
On Mon, Aug 19, 2024 at 12:54 AM ZhijieHanbioinfor @.***> wrote:
Dear Dr. Chu,
Thank you for your reply. I have another question. I want to merge multiple single cell samples as reference, which requires removing the batch effect. After removing the batch effect there will no longer be the counts values, will this have an effect on the BayesPrism analysis? Or the BayesPrism analysis doesn't need to remove the batch effect I mentioned. Thanks for your help.
Best,
Zhijie
Dr. Zhijie Han (韩智杰) Associate professor in Department of Bioinformatics School of Basic Medicine Chongqing Medical University, Chongqing, P.R. China @.***
------------------ Original ------------------ From: @.>; Date: Mon, Aug 19, 2024 10:46 AM To: @.>; Cc: @.>; @.>; Subject: Re: [Danko-Lab/BayesPrism] Can I used BayesPrism to perform deconvolution on the microarray results by the scRNAseq reference (Issue
96)
Dear user,
Thank you for your interest in our methods.
We have not tested if microarray data can be used as reference. We noted one recent study that applied BayesPrism to deconovovle the microarray bulk (https://www.biorxiv.org/content/10.1101/2023.06.14.544991v1.full), which seems to perform well. You may give it a try and see if the results make sense.
You may also try using markers when constructing the scRNA-seq reference to overcome the strong technical difference between RNA-seq and microarray data to see if it improves the results (provided you have some prior knowledge about the ground truth).
Best,
Tinyi
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Can I used BayesPrism to perform deconvolution on the microarray results (e.g., RMA expression values) by the scRNAseq reference? Suppose I take the relative expressions of RMA values and scRNAseq counts beforehand, respectively.