these posts are about genome assemblies, while the question was about a transcriptome assembly
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Hello everybody,
I have carried out an RNA-seq project in order to identify putative novel isoforms and genes in different plant annotations with TopHat/Cufflinks. Is there a way to assess the quality of my new annotations compared to the reference annotations?
Thank you.
Hi
Please see the old posts in Biostar itself, may be you have seen it already!
Best wishes
Sayuj
these posts are about genome assemblies, while the question was about a transcriptome assembly
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if I understood correctly, you're looking for new isoforms and genes in a species in which there's already an annotation available, right?. I guess you could try to do a de-novo assembly (ignoring the annotation) and see how this compares with the first one you did. how many transcripts are found again and how many counts are assigned to each of them.
I already have discovered new isoforms. I just want to assess which annotation is better (mine or the reference one) according to the FASTQ file or reads I used.