Thanks very much for your reply!
I will try these softwares and try to receive raw data!
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As the title...
Is "TPM" suitable for caculating DEG from different transcriptome researches but one specie?
It is not ideal. If you have nothing else than TPM then try limma-trend pipeline. Starting from raw counts is preferable. Please use the search function, this has literally been asked dozens of times before.
Thanks very much for your reply!
I will try these softwares and try to receive raw data!
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Hi,
Most of the softwares, such as edgeR and DESeq2, used to estimate DEG will require raw counts and, then, they will apply their own normalization methods.
António
Thanks very much for your reply!
I will try these softwares and try to receive raw data!