How to convert .ab1 to fastq
Good afternoon even
I actually need a help regarding How to convert ".ab1" file taken from sanger sequencing platform to its "fastq" file, with the original quality scoring for each based calls
I am doing it using chromas, SnapGene, Galaxy tools but I am not getting the correct form of fastq file could anybody please suggest me?
Or I have a doubt like whether it can be converted or not once after getting .ab1 file to fastq?
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2 answers
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try this gui tool: https://technelysium.com.au/wp/chromas/
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