Published May 31, 2005 | Version Supplemental Material + Submitted + Published
Journal Article Open

Subtree power analysis finds optimal species for comparative genomics

  • 1. ROR icon University of California, Berkeley

Abstract

Sequence comparison across multiple organisms aids in the detection of regions under selection. However, resource limitations require a prioritization of genomes to be sequenced. This prioritization should be grounded in two considerations: the lineal scope encompassing the biological phenomena of interest, and the optimal species within that scope for detecting functional elements. We introduce a statistical framework for optimal species subset selection, based on maximizing power to detect conserved sites. Analysis of a phylogenetic star topology shows theoretically that the optimal species subset is not in general the most evolutionarily diverged subset. We then demonstrate this finding empirically in a study of vertebrate species. Our results suggest that marsupials are prime sequencing candidates.

Additional Information

© 2005 The National Academy of Sciences. Communicated by Peter J. Bickel, University of California, Berkeley, CA, April 6, 2005 (received for review December 13, 2004) We thank Peter Bickel and Adam Siepel for helpful comments. M.I.J. was supported by National Institutes of Health Grant R33-HG003070. L.P. was supported by National Institutes of Health Grant R01-HG2362-3, a Sloan Foundation Research Fellowship, and National Science Foundation Career Award CCF-0347992. Author contributions: J.D.M., M.I.J., and L.P. designed research; J.D.M., M.I.J., and L.P. performed research; J.D.M., M.I.J., and L.P. contributed new reagents/analytic tools; J.D.M. analyzed data; and J.D.M. wrote the paper.

Attached Files

Published - PNAS-2005-McAuliffe-7900-5.pdf

Submitted - 0412012.pdf

Supplemental Material - 02790Fig3.pdf

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Additional details

Identifiers

PMCID
PMC1142384
Eprint ID
74831
DOI
10.1073/pnas.0502790102
Resolver ID
CaltechAUTHORS:20170307-090057219

Related works

Funding

NIH
R01-HG2362-3
Alfred P. Sloan Foundation
NSF
CCF-0347992

Dates

Created
2017-03-07
Created from EPrint's datestamp field
Updated
2021-11-11
Created from EPrint's last_modified field