The value of comparative genome analysis is becoming increasingly apparent in the derivation of gene structure and regulation data for use in developing treatments for human diseases—both inherited and acquired—and for understanding phylogeny and the mechanisms of evolution. Whole genome sequencing with multiple genome coverage is expensive, and the decision to sequence a specific organism involves questions of quantity versus quality of genome sequencing in the first world and questions of cost in the developing world. In the September 26
Kirkness et al. assembled 6.22 million sequence reads from the DNA of a standard poodle, and contigs and singletons were ordered with the scaffolder Bambus to yield 1.5x sequence coverage. Randomness...