Evolution and Population Genetics Seminar

Genetics 590

Autumn, 2001

The Evolution and Population Genetics seminar will meet on Tuesdays in Autumn quarter in Health Sciences Building J182 from 12:30pm - 1:20pm. This quarter the topic will be

Advanced Topics in Theoretical Evolutionary Genetics

The intention is to treat a number of topics in theoretical evolutionary genetics (theoretical population genetics) by reading papers from the literature and discussing them. Students in the course will be expected to lead one of these sessions, to do all readings, and to participate actively.

Some of the topics which are likely to be covered are:

Participants will read papers in this area and will be expected to lead discussion once during the quarter. Readings will be listed below.

The weekly references will be available to be copied in the copy room of the Genetics Department, J205 Health Sciences Building, and they are to be listed below.

The course will presuppose knowledge of elementary theoretical population genetics. It is a graduate course with prerequisite Genetics 562 or permission of the instructor.

Joe Felsenstein (joe@genetics.washington.edu)


Readings for coming sessions

Some of these are available on-line in electronic journals subscribed to by the University. The links here will lead to them. For those papers we will not make paper copies available: students should print their own.


October 2

Organizational meeting. At which peoples' attention will directed to the material below:


October 9

Two-locus theory: founding papers

Question to look into: are the equations in each of these papers exact or approximate for the models described?

October 16

Two-locus theory: further development

(the Lewontin paper is not available on-line). Questions: what generalizations were people trying to make? Did they succeed in finding them?


October 23

Diffusion approximations: why they work

(Neither of these is available on-line). Question: Does the method of asymptotically approaching the diffusion process give us a justification for it in cases where we are not at the asymptote?

October 30

Diffusion approximations: why they work (continued) (Presenter: Oliver Will)

(same references)


November 6

Variability in quantitative characters in natural populations (Presenter: Amy Anderson)

If you can get ahold of a copy of a recent edition (in the last few years) of my notes "Theoretical Evolutionary Genetics" for Genetics 562, and can read chapter XI, that will help with these papers.

Questions: Bulmer assumes (what?) part of the variance doesn't disappear under selection. What does this mean he is in effect assuming about number of loci, gene effects? Lande assumes that the distributions of gene effects remain normal. What does that assume about the strength of selection, and about mutation?


November 13

Variability in quantitative characters in natural populations, part II (presenter: Peter Beerli)

Barton, N. H. and M. Turelli . 1989. Evolutionary quantitative genetics: how little do we know? Annual Review of Genetics 23: 337-370.
(not available on-line)


November 20

Stepping-stone and continuum models with drift and mutation (presenter: Sacha Vignieri)


November 27

More on stepping-stone models: patch swamping and such (presenter: Chris Hess)

These papers are not available on-line.
Kimura and Maruyama: how much gene flow is needed to prevent local differentiation by genetic drift in different kinds of geographic structures?
Hanson: (This paper actually should have been put in the clines section, after the founding papers. Oops.) Under what circumstances can a patch of local adaptation by selection be eliminated by gene flow?


December 4

Clines: founding papers (presenter: Josh Whorley)

(In addition to thinking about clines, look in Wilkes's article for the mention of the Fisher paper. Are there any earlier examples of use of computers in biology?)

December 11

Clines: linkage and underdominance (presenter: Solly Sieberts)

How do different loci, each of which show geographic differentiation, arrange themselves in clines? Do they affect each other's pattern of geographic differentiation? Does this have any relevance to speciation?