Hi all,
I sequenced a genome on the Illumina MiSeq using paired ends. When analyzing the second read in FastQC, there is a steady increase of a over represented kmer (GGGGG).
Does anyone know what would cause this effect and whether it is indicative of an underlying problem?
I sequenced a genome on the Illumina MiSeq using paired ends. When analyzing the second read in FastQC, there is a steady increase of a over represented kmer (GGGGG).
Does anyone know what would cause this effect and whether it is indicative of an underlying problem?
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