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Question about calculate the immune cell fraction in bulk sequencing of tumor sample #95
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Dear user,
Thank you for your interest in our methods.
It is always recommended to use the most comprehensive representation of
cell types to build the scRNA-seq reference, as the statistical model
assumes that all cell types are found in the reference and their fractions
sum to one.
If only using non-tumor cells, the BayesPrism will distribute reads from
tumor cell to the cell type that are most similar to tumor cell in the
reference, and hence inflate its fraction.
I was not quite sure what is exactly meant when you say 3 cancer type.
Typically, it is recommended to deconvolve one cancer type, e.g. GBM or
lung cancer, at a time, using the scRNA-seq from the matched cancer type to
build the reference.
Best,
Tinyi
…On Mon, Aug 12, 2024 at 5:11 AM threshold233 ***@***.***> wrote:
Dear developers:
First of all, thank you for developing this great algorithms, it really
helped my research.
I try to find the specific immune cell fraction in a bulk dataset
containing multiple cancer.
But in this project, the reference scRNA dataset just contain 3 cancer
type, which means only 3 types of cancer cell can be included as the
reference for buliding the Prism object. But the bulk dataset containing 10
cancers.
So i wonder can i just use the non-tumor cells as the reference in
buliding the Prism object and what problem may this method cause in using
BayesPrism if i do not include the tumor cell.
Thanks for your help!
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Thank you for your explain, I know what i should for my assay. |
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Dear developers:
First of all, thank you for developing this great algorithms, it really helped my research.
I try to find the specific immune cell fraction in a bulk dataset containing multiple cancer.
But in this project, the reference scRNA dataset just contain 3 cancer type, which means only 3 types of cancer cell can be included as the reference for buliding the Prism object. But the bulk dataset containing 10 cancers.
So i wonder can i just use the non-tumor cells as the reference in buliding the Prism object and what problem may this method cause in using BayesPrism if i do not include the tumor cell.
Thanks for your help!
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