blat does have an option to do that, but the output is no different from BLAST, which is regions of alignment, not exons. As I understood from EvidenceModeler, raw blast output cannot be used as evidence, it needs exon boundaries so something has to convert it.
is there a way to get splice sites from BLAST results?
Does anyone know a program that can turn blast output into predicted transcripts with splicing sites?
I imagine some kind of program that can map blast hits (either blastn or tblastn) and then extend the hits in both directions to find optimal/ realistic splice sites.
Exonerate is unbelievably slow, and since blast already finds the best site very quickly, something that could just 'optimize' the transcripts/proteins to the genome would be great.
I find it hard to believe that something like this does not already exist.
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Take a look at blat - it may have an option to align protein onto genomic.
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To follow up, there is a specific program to do this called genBlastG, however it is long depricated (as far as I can tell); it has not been updated in years and the creator is not responding to email.
The program itself crashed for every version that I tried, so it is unlikely that this will be a viable option.