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-   -   454 gsAmplicon Editing Reads (http://seqanswers.com/forums/showthread.php?t=50193)

styagi 02-09-2015 09:54 AM

454 gsAmplicon Editing Reads
 
Does anyone know how to edit reads after alignment has been done using gsAmplicon software? I want to go back and edit any variants that I know are sequencing errors.

styagi 02-09-2015 10:56 AM

I just found that there is no function to edit reads on the 454 software. Does anyone know a program that would allow me to edit reads post alignment. I dont want filter out the reads completely, I want to be able to edit the errors and use them for alignment and analysis.

Zaag 02-10-2015 06:17 AM

Well if that really is what you want you could go from sff to fasta, alter the fasta and go back to sff. You can use the sfftools/sffinfo provided by Roche.

styagi 02-10-2015 07:42 AM

I thought sfftools was only provided with the 454 machine which I dont have. I had my samples sequenced at a core bioinformatics lab.

Zaag 02-10-2015 07:49 AM

From what I understand they'll give you the programs you need if you ask nicely:

http://seqanswers.com/forums/showpos...8&postcount=13

I think there also are some open source variants of the tools but I never used them.

styagi 02-10-2015 08:21 AM

I will look into that.
thank you for your help!

martin2 06-17-2015 07:42 AM

Quote:

Originally Posted by Zaag (Post 159949)
Well if that really is what you want you could go from sff to fasta, alter the fasta and go back to sff. You can use the sfftools/sffinfo provided by Roche.

You can't go back from FASTA/Q and re-create SFF. In theory you could but nobody wrote such code yet. As far as I am aware of the status in biopython, Roche sfftools, flower.


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