Additionally: I wonder if homology-based primary genome annotation software may 
be relevant? E.g. Genewise (Wise2 package) tries to find a plausible gene 
structure AND a decent level of sequence similarity.

http://www.ebi.ac.uk/Tools/psa/genewise/help

I know Exonerate less well, but I expect it can do similar things and more 
(likely more rapidly):

https://www.ebi.ac.uk/~guy/exonerate/

Presumably these packages have settings about whether introns are expected or 
not (eukaryotic genomic DNA vs transcript sequence), specific penalties, etc.

There are other tools for prokaryotes, I think.

- Daniel

Daniel Barker
http://biology.st-andrews.ac.uk/staff/db60
The University of St Andrews is a charity registered in Scotland :
No SC013532

________________________________________
From: [email protected] 
[[email protected]] on behalf of David 
Bauer [[email protected]]
Sent: 01 October 2014 06:47
To: Warren Gallin; [email protected]
Subject: Re: [EMBOSS] needle extended with reading frame information?

Hi,

did you try the EMBOSS tranalign ?

tranalign       Generate an alignment of nucleic coding regions from aligned 
proteins

Kind regards,
David.

-----Ursprüngliche Nachricht-----
Von: [email protected] 
[mailto:[email protected]] Im Auftrag 
von Warren Gallin
Gesendet: 30 September 2014 22:51
An: [email protected]
Betreff: Re: [EMBOSS] needle extended with reading frame information?

It might be more useful to you to align the protein sequences and then thread 
the corresponding nucleotide sequences onto that AA alignment "skeleton"

Translator X will do this for you automatically, given the ORFs, or you can 
provide a pre-run protein alignment if the alignment programs in TranslatorX 
are not suitable for you.

http://translatorx.co.uk/

You can either run on their server or, if your job is too big, download and 
install locally.

Warren Gallin

On Sep 30, 2014, at 2:27 PM, Adam Sjøgren <[email protected]> wrote:

>  Hi.
>
> I want to align a DNA sequence where I know where the reading frame is,
> with another DNA sequence.
>
> In the alignment I would prefer gaps to be opened/ended on codon
> boundaries (avoiding as much as I can what would be frameshifts).
>
> I.e. in a simple example, I would prefer:
>
>  GATGATTTTGA           GATGATTTTGA
>  ||||||   ||    over   |||||   |||
>  GATGAT---GA           GATGA---TGA
>  12312312312           12312312312   <-- reading frame pos
>
> One way I guess the alignment could be nudged to give me results closer
> to what I want, is to have a gap open penalty which depends on the
> position in the reading frame.
>
> Has anyone played around with this, or done something along these lines?
>
>  Best regards,
>
>    Adam
>
> P.S. It seems that emboss.open-bio.org no longer accepts email?
>
> --
> "Sadly, these days, if you know the difference               Adam Sjøgren
>  between a phillips- and a flat head screwdriver,       [email protected]
>  you're a renaissance man."
>
> _______________________________________________
> EMBOSS mailing list
> [email protected]
> http://mailman.open-bio.org/mailman/listinfo/emboss


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