Hi,
FASTQC can provide duplicate sequences during quality control of fastq data. But not all of them are really "unique" (=some of them are only partial sequences of a larger parental sequence (e.g. a contamination)). If I put all duplicate sequences in a text file (or FASTA), is it possible to "merge" those sequences by means of any software? thank you
(I allready tried Muscle but it seems to be not what i want)
FASTQC can provide duplicate sequences during quality control of fastq data. But not all of them are really "unique" (=some of them are only partial sequences of a larger parental sequence (e.g. a contamination)). If I put all duplicate sequences in a text file (or FASTA), is it possible to "merge" those sequences by means of any software? thank you
(I allready tried Muscle but it seems to be not what i want)
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