The accuracy of large-scale DNA sequencing is difficult to estimate without
redundant effort. We have found that the mobile genetic element IS10, a co
mponent of the transposon Tn10, has contaminated a significant number of cl
ones in the public databases, as a result of the use of the transposon in b
acterial cloning strain construction. These contaminations need to be annot
ated as such. More positively, by defining the range of sequence variation
in IS10, we have been able to determine that the rate of sequencing errors
is very low, most likely surpassing the stated aim of one error or less in
ten thousand bases.