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I normally trim the first and last 5bp of reads for this reason (to avoid miscalled indels at the tips), after the reads are aligned. If you don't realign around indels, I recommend this. Might be a good idea even if you do realign; even with realignment, there are some features that you cannot resolve, since there is not enough information at the read tips.
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Local realignements are helpful not because of sequencing quality concerns, but because of the general difficulty to get alignments right around indels, especially towards the end of reads .
Btw, just saw this nice paper: http://journals.plos.org/plosone/art...l.pone.0075402
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Exome sequencing: should we do local realignment
Dear colleagues,
With ever-increasing quality of NGS platforms, is it still desirable to do local realignment for HiSeq 2500 human exome reads from an Agilent Sureselect library?
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