Hi Bala

No, this is only for DNA sequence comparisons.

Regards
Tim


On 7/11/06 12:02, "BALASUBRAMANIAN GANESAN" <[EMAIL PROTECTED]> wrote:

> Dear Tim/Julian/users
> Is it also possible to use protein sequence comparisons using this same
> approach?
> Regards
> BALA.
>> ===== Original Message From Julian Parkhill <[EMAIL PROTECTED]> =====
>> Bala,
>> 
>> ACT cannot reconstruct the positional information for the separate
>> sequences within a multiple FASTA file; BLAST reports only the local
>> coordinates for the matches. What you need to do is:
>> 
>> 1) Concatenate all the mFASTA sequences into a single sequence for
>> each genome (you can do this from Artemis, using the "Write; all
>> bases" menu)
>> 
>> 2) Do the blast comparison with the concatenated sequences
>> 
>> 3) Load the original multiple FASTA files into ACT, but use the
>> comparison file from the concatenated sequences. You should see the
>> contigs represented by alternating dark/light brown features, plus
>> the matches for the whole sequences.
>> 
>> For the other problem; the set cutoffs only remain for as long as the
>> dialog window is open. Closing the dialog window resets the cutoffs.
>> 
>> yours,
>> 
>> Julian.
>> 
> 



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