An increasing interest in gene expression profiles in human diseases has le
d to the use of microdissected tumors and biopsies in gene discovery approa
ches. Since many of these clinical samples yield extremely small amounts of
RNA, reproducible methods are needed to amplify this RNA while maintaining
the original message profile. Using the SMART(TM) cDNA Synthesis Method, w
e show that high-, medium- and low-abundance transcripts can be amplified i
n a representative fashion and that the resulting cDNA can also be used as
a complex probe to confirm gene expression differences identified by other
techniques.