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Resolution: standard / high Figure 3.
CGH analyses. A) For each species, genomic DNAs from each animal (n = 4) were hybridized on separate
arrays against a reference DNA from pooled zebra finches. Histograms are shown of
the resulting mean log2 ratios (zebra finch:test species) for all gene targets, by
test species. Note that when samples from individual zebra finches were hybridized
versus the pooled zebra finch reference, the log2 signal ratios cluster closely around
0 as expected. The curve becomes shorter and broader with cross-hybridization to the
kingbird and the chicken. B) Histograms of log2 ratios (zebra finch:test species)
for a subset of 200 spots found significantly different on multi-species analysis
of CGH data. Significant spots were determined by multi-class SAM Analysis using TIGR
TMEV software with a median number of false significant genes set at 0. Note the large
shift of the distribution to the right with increasing phylogenetic distance. C) Hierarchical
tree of all CGH arrays, in a multiclass analysis using the Euclidean distance metric
with average linkage clustering [82]. Arrays from the same species are clustered together,
and the hierarchy is consistent with phylogenetic species relationships. The autologous
hybridization (zebra finch – zebra finch, not shown) is effectively the outgroup in
this analysis. D) The distribution of log2 ratios (test species:zebra finch reference)
for one spot across 28 arrays (7 species).
Replogle et al. BMC Genomics 2008 9:131 doi:10.1186/1471-2164-9-131 |