Part of a typical set of input data. The input data consists of 13 rows. The first row contains sequence from the target genome, the second to twelfth rows contain aligned sequence from informant genomes and the last row encodes information about the alignments of ESTs to the target genome.
Gross et al. Genome Biology 2007 8:R269 doi:10.1186/gb-2007-8-12-r269