The BARE-1 retrotransposon is an active. dispersed, and highly abundant com
ponent of the genome of barley (Hordeum vulgare) and other species in its g
enus. Like all retrotransposons of its kind, BARE-1 is bounded by long term
inal repeats (LTRs). We have developed two amplification-based marker metho
ds based on the position of given LTRs within the genome. The IRAP (Inter-R
etrotransposon Amplified Polymorphism) markers are generated by the proximi
ty of two LTRs using outward-facing primers annealing to LTR target sequenc
es. In REMAP (REtrotransposon-Microsatellite Amplified Polymorphism), ampli
fication between LTRs proximal to simple sequence repeats such as constitut
e microsatellites produces markers. The methods can distinguish between bar
ley varieties and produce fingerprint patterns for species across the genus
. The patterns indicate that although the BARE-1 family of retrotransposons
is disperse, these elements are locally clustered or nested and often foun
d near tandem arrays of a simple sequence repeat.