Open NJU-Bio-Info opened 2 years ago
Thank you for the question. The .sf
file is the output from salmon
. For example, the rule salmon_quant_pe
will generate this by running the salmon quant
command.
I will add a README file in the next days, to describe more in detail how the pipeline is run. Note that what is currently the normalize
is what was used in the final analysis. I will eventually move this too main
. I'll let you know when I've updated, but free feel to ask any more clarifications!
Yeah, I really want to learn from your scripts about how to identify different polyA sites usage(or transcript isoform) with the output of QAPA. If you can make some clarification for this topic, you will help me a lot about my project!!! Really want to see your update!
The index for salmon used to generating .sf file in DEXseq.R and DESeq.R is the output utr sequence(.fa file)? or the whole genome(transcriptome)?
That's a good question. I'll make sure to include the provenance for that in the write-up.
The index is from the QAPA v1.3.0 release, then using the UCSC mm10 genome as a decoy. The steps to replicate the index are documented in the Snakefile in my mm10-db
repository.
Hi, when I learn your R scripts about DESeq and DEXSeq, I wonder that the quant.sf file here is the output of qapa?