Hi everybody,
I relatively new to this, so I thought I'd ask about way to solve my problem in the most easy way.
I have *.ab1 files from an Applied Biosystem's 3730xl DNA Analyzer from different individuals for different genes each sequenced with a forward and a reverse primer.
In the past I constructed the consensus sequences by hand in BioEdit while looking at the chromatogram in Geospiza's FinchTV but that's a lot of work and quite subjective.
I thought there must be an easier and more objective way to do this... Is there a way/workflow to automatically combine my two reads per gene and individual in a consensus sequence using some kind of objective quality score and outputting that as a FASTA file or similar? Ideally, there should be a way to flag heterozygotes, too.
Any help would be greatly appreciated.
I relatively new to this, so I thought I'd ask about way to solve my problem in the most easy way.
I have *.ab1 files from an Applied Biosystem's 3730xl DNA Analyzer from different individuals for different genes each sequenced with a forward and a reverse primer.
In the past I constructed the consensus sequences by hand in BioEdit while looking at the chromatogram in Geospiza's FinchTV but that's a lot of work and quite subjective.
I thought there must be an easier and more objective way to do this... Is there a way/workflow to automatically combine my two reads per gene and individual in a consensus sequence using some kind of objective quality score and outputting that as a FASTA file or similar? Ideally, there should be a way to flag heterozygotes, too.
Any help would be greatly appreciated.
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