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While there is no specific rule against the use of ChatGPT or similar, this must be clearly stated in the answer
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As you managed to run each organism separately successfully. Does the combined size of the FASTA files exceed the amount of memory you spec…
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Oh come on...
https://www.biostars.org/p/75548/
https://www.biostars.org/p/357878/
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Your idea is definitely feasible on Illumina reads. Since curated chimera datasets are rare, most people simulate them in silico (concatena…
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Your answer should be the top-voted answer in this thread https://www.biostars.org/p/284775/ as it actually addresses conceptual diffe…
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> I am not sure if there would be primer dimer sequences
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that 151st base added is a base to ignore (it's a kind of random addition) ... if I recall correctly it's a consequence of the technology. …
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@swbarnes2 Thank you for your response! I am new to RNA seq analysis and was originally recommended to use the LM method following cqn and …
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Thank you very much.
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Because there wasn't RNA-seq analysis performed for every sample in TCGA?
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I cannot guide on GraphPad. It's commercial software so better contact their support.
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DE genes in bulk RNASeq is what DESeq2 was made for, so why wouldn't you use it? RPKM is not an appropriate normalization method here.
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