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Description
Dear Patcher-lab,
I have used some pantranscriptomics tool to map RNA-seq reads on a pangenome graph, from this paper and that github.
The final output I have is a table giving read counts, effective length, as well as other features :
target_id length eff_length ReadCounts tpm
transcript_1 1012 536.576 359.436 26.4885
transcript_2 416 146.094 21 5.684
transcript_3 1353 1017.84 0 0
...
For some reasons, I could not use kallisto
on my data, and I rather had to use the aforementionned tools. I am now wondering whether I could still use sleuth
on the output I have.
In particular
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Do you so any strong reason to not try using
sleuth
on those outputs? -
I think I would have to transform my read counts into estimated read counts similar to the ones given by
kallisto
- is there anyway to do this with the info I have ?
Thank you for reading me.
Edit: there were errors in the table I have; the output is in Read Count and not estimated counts (else I could directly use sleuth
).