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@loganylchen
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No need to calculate the gene len if the file already provided.

@poseidonchan
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Hi Logan,

Thanks for your commit, but I am considering removing these function, calculating the TPM or FPKM seems useless?

Yanshuo

@loganylchen
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Hi Yanshuo,

I don't have any solid evidence for the necessity of converting counts to TPM or FPKM. But I saw many other deconvolution tools accept raw counts as their first priority input format.

Considering the pseudo-bulk differential expressed gene identification in general single-cell analysis, I think it should be OK, or reasonable to treat the count matrix from both single-cell and bulk RNA-seq following the same distribution. Maybe we could have some tests if the predictions perform better with/without transforming.

Logan

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2 participants