Why quality of the reads gets dropped at the end?
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I often heard that "alignment of sequence reads to a reference can be inaccurate towards the ends of a read", does anybody know the exact reason of this?
One reason would be that the quality of the reads gets dropped at the end. Its because of the sequencing chemistry.
Hence for e.g, a 100 bp read will have low quality bases at the end (10-20 bases). Its good to see the box plot of quality score and trim off the bases if necessary before alignment.
Why quality of the reads gets dropped at the end?
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Cross-posted on SeqAnswers