Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome

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Figure 5.
Figure 5.

Alignment “correctness” as measured by Alu exclusion and periodicity of substitutions in coding exons. For a group of non-primate mammals, the fraction of human Alu bases (out of a total of ∼3.8 million) that are not aligned (i.e., gapped) is shown (top panel). A score of 1 would correlate with complete exclusion of all Alus, as would be the case in alignments with no false-positive orthology predictions. We also show the fraction of human coding exons that show a triplet periodicity in substitutions in the pairwise alignment between human and each query species (see Methods). Note that this is purely a relative measure, since we exclude exons that are completely gapped in at least one alignment, or fail to show periodicity in at least one alignment.

This Article

  1. Genome Res. 17: 760-774

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