Does anybody knows why, why base quality drops towards the end for Illumina reads?
Does anybody knows why, why base quality drops towards the end for Illumina reads?
The illumina platform uses a so called sequencing by synthesis process. Bases are added one at a time and the consensus is determined in a cluster of identical sequences.
The source of errors can be numerous, here is one review that discusses the issues in more detail:
The challenges of sequencing by synthesis, Nature Biotech, 2009
In a nuthsell a short answer to the best of my understanding is this: Not all sequences in a cluster will grow at the same rate, this will slowly lead to a desynchronization as the errors accumulate. This is why the quality dips towards the end.
See this post: Why does base quality of reads generally decreases at the end of the read?
I'd highly recommend you check out this - The site as a whole is useful for explaining common things you'd see in sequencing, like primer bias.
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Good question - I have always accepted the phenomenon without really understanding the cause.