Advances in DNA sequencing and the near-term availability of whole genome s
equences for several pharmaceutically relevant organisms promise to dramati
cally alter the breadth and scale of high-throughput proteomic studies. The
substantial amount of literature is available in the public domain, demons
trate the potential of proteomics in the preclinical phases of pharmaceutic
al development. Over the next few years, it is anticipated that functional
genomics and proteomics will have major impacts on the clinical phases of d
rug development. Expected benefits are earlier proof-of-concept studies in
man and increased efficiency of clinical trials through the availability of
biologically relevant markers for drug efficacy and safety.