Entering edit mode
Hello list members,
For a RNA-seq analysis, what would you suggest to use to convert raw-
sequence-based read coverage to annotated ORF-based coverage, if the
genome of interest is NOT supported in neither UCSC nor ENSEMBL, which
means that creation of a TranscriptDB object in a straightforward way
(I.e. according to the GenomicFeatures pipeline) is impossible? What
would you recommend to import a .gff file (containing annotation of a
particular genome, from GenBank) into R/Bioconductor to eventually
generate a gene-centric countTable readable by packages like DESeq?
Thank you!
Oleg
[[alternative HTML version deleted]]