This proposal develops software tools, which use Markov Chain Monte Carlo (MCMC) maximum-likelihood methods to infer population parameters from genetic data. We focus specifically on inferring selection and on mapping both known traits and unknown selective influences to specific chromosomal regions. We will develop new techniques for the following: (1) Estimating the presence and strength of natural selection and the degree of dominance, including statistical tests to compare selection hypotheses. (2) Mapping the location of a measured trait, or of a selection effect, relative to markers on a haplotype. (3) Mining the large sample of genealogies produced by MCMC algorithms for information such as the location of recombination hotspots, the time of significant events such as disease-locus mutations, and the overall time distribution of migration, mutation and recombination events. (4) Improving performance of MCMC algorithms via better search strategies and use of multiple computers in parallel. (5) Incorporating analysis of serial samples (samples taken from a population at different times) in order to strengthen estimation of selection and population growth. We will create freely distributed software implementing these methods and will test them using real and simulated data.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM051929-11
Application #
6930587
Study Section
Genetics Study Section (GEN)
Program Officer
Eckstrand, Irene A
Project Start
1995-01-01
Project End
2007-08-31
Budget Start
2005-09-01
Budget End
2006-08-31
Support Year
11
Fiscal Year
2005
Total Cost
$481,367
Indirect Cost
Name
University of Washington
Department
Genetics
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
McGill, James R; Walkup, Elizabeth A; Kuhner, Mary K (2013) Correcting coalescent analyses for panel-based SNP ascertainment. Genetics 193:1185-96
Kuhner, Mary K (2009) Coalescent genealogy samplers: windows into population history. Trends Ecol Evol 24:86-93
Smith, Lucian P; Kuhner, Mary K (2009) The limits of fine-scale mapping. Genet Epidemiol 33:344-56
Kuhner, Mary K; Smith, Lucian P (2007) Comparing likelihood and Bayesian coalescent estimation of population parameters. Genetics 175:155-65
Kuhner, Mary K (2006) Robustness of coalescent estimators to between-lineage mutation rate variation. Mol Biol Evol 23:2355-60
Kuhner, Mary K (2006) LAMARC 2.0: maximum likelihood and Bayesian estimation of population parameters. Bioinformatics 22:768-70
Felsenstein, Joseph (2006) Accuracy of coalescent likelihood estimates: do we need more sites, more sequences, or more loci? Mol Biol Evol 23:691-700
Felsenstein, Joseph (2005) Using the quantitative genetic threshold model for inferences between and within species. Philos Trans R Soc Lond B Biol Sci 360:1427-34
Beerli, Peter (2004) Effect of unsampled populations on the estimation of population sizes and migration rates between sampled populations. Mol Ecol 13:827-36
Felsenstein, J (2001) Taking variation of evolutionary rates between sites into account in inferring phylogenies. J Mol Evol 53:447-55

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