Entering edit mode
1 day ago
dr.suvarnakapale
•
0
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?