Figure 4.

Insert size showing steric hindrance. (a) Insert size was generated from libraries spiked into a paired-end 101 bp run resulting in a large proportion of reads reading into the adaptor sequence. Tails of reads were then aligned to one another to discern the insert size between adaptors, resulting in a mapping-independent insert size at the lower extreme. All reads with an insert size less than 25 bp were PCR artifacts. (b) The noticeable drop below 40 bp is consistent with a model for complete saturation of transposition events on a given stretch of DNA. The roughly 110 Å transposase homodimer (grey) is bound to genomic DNA (blue), such that the core of the enzyme acts on a 9 bp region drawn out to 41 Å as well as approximately 10 additional bases of DNA flanking either side (~34 Å each) that are essentially protected from a subsequent transposase attack due to steric hindrance. Since the core region is duplicated in the process, the minimum spacing of transposition events is approximately 38 bp.

Adey et al. Genome Biology 2010 11:R119   doi:10.1186/gb-2010-11-12-r119
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