Re: [Transdecoder-users] Using BLASTN evidence for CDS predictions
Extracting likely coding regions from transcript sequences
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From: <Ale...@cs...> - 2014-06-25 01:39:53
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Hi Martin >Yes, I don't mind it would resurrected mistakenly truly dead genes (pseudogenes). I think that might be a bit out of the scope of the TransDecoder program as a lot of people would mind. Creating a second software that uses the TransDecoder output and the transcriptome assembly sounds like a better way to do it. a ________________________________________ From: Martin MOKREJŠ [mmo...@gm...] Sent: Tuesday, 24 June 2014 11:11 PM To: tra...@li... Subject: Re: [Transdecoder-users] Using BLASTN evidence for CDS predictions Martin MOKREJŠ wrote: > Hi, > I wonder whether TransDecoder could also run blastn against a somewhat related genome/transcriptome > and considered the matching regions. They will be matching exons and the UTRs won't be conserved. > > Further, could TransDecoder ignore a STOP codon and merge two ORFs if the macthes are in adjacent > frames on the same target strand? Aha, forgot to explain a bit more: the alignment to DNA will reveal gaps in either strand so quite helpful hint for an artificial insertion/deletion. It should be easy for TransDecoder to realize that at that position is likely an error. Yes, I don't mind it would resurrected mistakenly truly dead genes (pseudogenes). Martin ------------------------------------------------------------------------------ Open source business process management suite built on Java and Eclipse Turn processes into business applications with Bonita BPM Community Edition Quickly connect people, data, and systems into organized workflows Winner of BOSSIE, CODIE, OW2 and Gartner awards http://p.sf.net/sfu/Bonitasoft _______________________________________________ Transdecoder-users mailing list Tra...@li... https://lists.sourceforge.net/lists/listinfo/transdecoder-users |