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7.2 years ago
bharath.mh24
•
0
Hello, I was wondering if there was some way I could map single end reads in fastq format to combination of primers (Artificial Reference Genome) in fasta format without much coding. I would like the output to be the pair of matched sequences' identifiers (Sequence names). Is there some tool to do so? Any suggestions would be really helpful. Thank You for your time
