Archive of newsgroup
From joe@evolution.genetics.washington.edu Fri Feb 7 23:13:41 PST 1997 Article: 20 of uwash.class.genet453 Path: news.u.washington.edu!evolution.genetics.washington.edu!joe From: joe@evolution.genetics.washington.edu (Joe Felsenstein) Newsgroups: uwash.class.genet453 Subject: Hello Date: 8 Jan 1997 14:29:27 GMT Organization: University of Washington Genetics Lines: 14 Message-ID: <5b0b07$6vp@nntp3.u.washington.edu> NNTP-Posting-Host: evolution.genetics.washington.edu Summary: Introduction This newsgroup is now ready for business. I am asked by C&C to remind you that you are not to abuse the use of this newsgroup in any of a variety of ways. If you have functional questions about the course, or any question at all about the lecture material, please post here and I will try to answer, or you can answer each other. By the way, I also hope to announce office hours very soon, as soon as I can find any. It will probably be on Thursdays early afternoon. -- Joe Felsenstein joe@genetics.washington.edu (IP No. 128.95.12.41) Dept. of Genetics, Univ. of Washington, Box 357360, Seattle, WA 98195-7360 USA From joe@evolution.genetics.washington.edu Fri Feb 7 23:14:33 PST 1997 Article: 21 of uwash.class.genet453 Path: news.u.washington.edu!evolution.genetics.washington.edu!joe From: joe@evolution.genetics.washington.edu (Joe Felsenstein) Newsgroups: uwash.class.genet453 Subject: Office hours and web page Date: 13 Jan 1997 18:58:21 GMT Organization: University of Washington Genetics Lines: 10 Message-ID: <5be0kd$50d@nntp3.u.washington.edu> NNTP-Posting-Host: evolution.genetics.washington.edu Summary: Now available The class web page is now available. It is, as we announced, at http://weber.u.washington.edu/~genetics/courses/genet453/1997/genet453.html I will have office hours every Thursday from 2-3 in my office (J253 HSB). This is right down the hall from the lecture room. I will, however, be away on January 16. --- Joe Felsenstein joe@genetics Department of Genetics, Box 357360 From joe@evolution.genetics.washington.edu Fri Feb 7 23:19:08 PST 1997 Article: 22 of uwash.class.genet453 Path: news.u.washington.edu!evolution.genetics.washington.edu!joe From: joe@evolution.genetics.washington.edu (Joe Felsenstein) Newsgroups: uwash.class.genet453 Subject: Office hours (revised) Date: 22 Jan 1997 19:02:15 GMT Organization: University of Washington Genetics Lines: 8 Message-ID: <5c5o7n$95v@nntp3.u.washington.edu> NNTP-Posting-Host: evolution.genetics.washington.edu Summary: Half an hour later The office hours for this class have been changed to 2:30-3:30 Thursdays. This is to avoid conflict with a seminar that I am attending. Thus they are half an hour later than previously announced. -- Joe Felsenstein joe@genetics.washington.edu (IP No. 128.95.12.41) Dept. of Genetics, Univ. of Washington, Box 357360, Seattle, WA 98195-7360 USA From jonmac@u.washington.edu Fri Feb 7 23:19:24 PST 1997 Article: 23 of uwash.class.genet453 Path: news.u.washington.edu!root From: jonmac@u.washington.edu (Jonathan McBride) Newsgroups: uwash.class.genet453 Subject: first student to post a message Date: Tue, 28 Jan 1997 05:09:23 GMT Organization: University of Washington Lines: 8 Message-ID: <32ee88e4.19068096@news.u.washington.edu> NNTP-Posting-Host: cs238-15.student.washington.edu Mime-Version: 1.0 Content-Type: text/plain; charset=us-ascii Content-Transfer-Encoding: 7bit X-Newsreader: Forte Agent .99g/32.339 I've been checking the news group for a week now and no one has posted a message, so I thought I would start things off. I don't really have anything to say, just that I downloaded the simul8 program this afternoon and everything went well. From joe@evolution.genetics.washington.edu Fri Feb 7 23:15:10 PST 1997 Article: 24 of uwash.class.genet453 Path: news.u.washington.edu!evolution.genetics.washington.edu!joe From: joe@evolution.genetics.washington.edu (Joe Felsenstein) Newsgroups: uwash.class.genet453 Subject: Re: first student to post a message Date: 28 Jan 1997 07:21:59 GMT Organization: University of Washington Genetics Lines: 16 Message-ID: <5ck9en$k7e@nntp3.u.washington.edu> References: <32ee88e4.19068096@news.u.washington.edu> NNTP-Posting-Host: evolution.genetics.washington.edu Summary: Hooray In article <32ee88e4.19068096@news.u.washington.edu>, Jonathan McBridewrote: > >I've been checking the news group for a week now and no one has posted >a message, so I thought I would start things off. > >I don't really have anything to say, just that I downloaded the simul8 >program this afternoon and everything went well. Congratulations on being first! I *had* wondered whether student *could* post. Now I know. Anyone with further experiences with simul8 should post here. -- Joe Felsenstein joe@genetics.washington.edu (IP No. 128.95.12.41) Dept. of Genetics, Univ. of Washington, Box 357360, Seattle, WA 98195-7360 USA From jonmac@u.washington.edu Fri Feb 7 23:15:26 PST 1997 Article: 25 of uwash.class.genet453 Path: news.u.washington.edu!root From: jonmac@u.washington.edu (Jonathan McBride) Newsgroups: uwash.class.genet453 Subject: simul8 Date: Wed, 29 Jan 1997 05:31:46 GMT Organization: University of Washington Lines: 16 Message-ID: <32eede73.3089022@news.u.washington.edu> NNTP-Posting-Host: cs207-22.student.washington.edu Mime-Version: 1.0 Content-Type: text/plain; charset=us-ascii Content-Transfer-Encoding: 7bit X-Newsreader: Forte Agent .99g/32.339 I've been fiddling around with the simul8 program tonight and I discovered that what Professor Felsenstein said was right (I guess that is why he is the professor). I ran 20 simulation with the fitnesses all equal and the beginning gene frequency at 0.5 but with a migration rate of 0.5 also. From the first 10 runs, I only got "a" fixed twice (so I was a little skeptical of the program). But in the next 10 runs the "a" allele was fixed 6 more times. I suppose that if I would have kept doing simulations, it would have evened out so that half would be fixed at "A" and the other half would be fixed at "a". I do have one question, though, why is the gene frequeny of the immigrating population not a variable that affects this scenetio? Intuatively it seems like it should be. Is it just assumed to be the same as in the main population? jonmac@u.washigton.edu From joe@evolution.genetics.washington.edu Fri Feb 7 23:16:05 PST 1997 Article: 26 of uwash.class.genet453 Path: news.u.washington.edu!evolution.genetics.washington.edu!joe From: joe@evolution.genetics.washington.edu (Joe Felsenstein) Newsgroups: uwash.class.genet453 Subject: Re: simul8 Date: 29 Jan 1997 08:53:30 GMT Organization: University of Washington Genetics Lines: 24 Message-ID: <5cn36a$min@nntp3.u.washington.edu> References: <32eede73.3089022@news.u.washington.edu> NNTP-Posting-Host: evolution.genetics.washington.edu Summary: Migration, how it works In article <32eede73.3089022@news.u.washington.edu>, Jonathan McBride wrote: > I do have one question, though, why is the gene frequeny of >the immigrating population not a variable that affects this scenetio? >Intuatively it seems like it should be. Is it just assumed to be the >same as in the main population? By the "immigrating population" I think you mean the population that is the source of the migrants. I guess I didn't make it clear that when there are (say) 8 populations, and a migration rate of m = 0.1, that means that 0.10 of the individuals in each population come from a random mixture of all 8 populations. That is, each migrant in effect is drawn at random >from the species as a whole. Thus migration makes the populations' gene frequencies get closer to each other, not to some source population's gene frequencies. There are other ways to model migration, and in the Mac version that I demonstrated in class, there are ways you can do the source-population case, but iin Simul8 it's done only one way, they way described above. -- Joe Felsenstein joe@genetics.washington.edu (IP No. 128.95.12.41) Dept. of Genetics, Univ. of Washington, Box 357360, Seattle, WA 98195-7360 USA From jonmac@u.washington.edu Thu Feb 27 07:16:47 PST 1997 Article: 27 of uwash.class.genet453 Path: news.u.washington.edu!root From: jonmac@u.washington.edu (Jon McBride) Newsgroups: uwash.class.genet453 Subject: migration Date: Sun, 09 Feb 1997 19:31:18 GMT Organization: University of Washington Lines: 20 Message-ID: <32fe224b.1304965@news.u.washington.edu> NNTP-Posting-Host: cs201-6.student.washington.edu Mime-Version: 1.0 Content-Type: text/plain; charset=us-ascii Content-Transfer-Encoding: 7bit X-Newsreader: Forte Agent .99g/32.339 I was just playing around with the simul 8 program again and I was experimenting by progressively increasing the migration rate. The degree to which the respective populations changed relative to each other (differentiated) decreased as the migration rate increased. I kept the population size the same. I was trying to think of an explanation for this observation, and I would like to know if it is a sound interpretation or not. If the migration rate is high (say 0.8) between 8 populations of 1000, isn't it the same as having a population of nearly 8000? If there is complete migration (1.0) it would be exactly the same because the whole idea of a subpopulation is meaningless. So, in a way, one could think of migration as a restriction that is placed on a population of individuals to limit the extent that they breed (m = 1-r) and, in effect, creating subpopulations. Then one would expect, as I observed in the simulation, the differentiation of the simulated populations to be small. Jon McBride jonmac@u.washigton.edu From joe@evolution.genetics.washington.edu Thu Feb 27 07:17:13 PST 1997 Article: 28 of uwash.class.genet453 Path: news.u.washington.edu!evolution.genetics.washington.edu!joe From: joe@evolution.genetics.washington.edu (Joe Felsenstein) Newsgroups: uwash.class.genet453 Subject: Re: migration Date: 10 Feb 1997 06:27:20 GMT Organization: University of Washington Genetics Lines: 36 Message-ID: <5dmf48$4g2@nntp3.u.washington.edu> References: <32fe224b.1304965@news.u.washington.edu> NNTP-Posting-Host: evolution.genetics.washington.edu Summary: Yup Keywords: migration, population genetics In article <32fe224b.1304965@news.u.washington.edu>, Jon McBride wrote: >I was just playing around with the simul 8 program again and I was >experimenting by progressively increasing the migration rate. The >degree to which the respective populations changed relative to each >other (differentiated) decreased as the migration rate increased. I >kept the population size the same. I was trying to think of an >explanation for this observation, and I would like to know if it is a >sound interpretation or not. Very sound. It's what you expect. When m is zero, they wander off independently. When m is large, theye act like parts of one big population. In that case they have almost the same gene frequency at all times. >If the migration rate is high (say 0.8) between 8 populations of 1000, >isn't it the same as having a population of nearly 8000? If there is >complete migration (1.0) it would be exactly the same because the >whole idea of a subpopulation is meaningless. Correct. >So, in a way, one could >think of migration as a restriction that is placed on a population of >individuals to limit the extent that they breed (m = 1-r) and, in >effect, creating subpopulations. Then one would expect, as I observed >in the simulation, the differentiation of the simulated populations to >be small. Well, you would expect that, but I don't find it any clearer than just thinking about migration. But 30 years in the field may have warped my idea of what is clear ... -- Joe Felsenstein joe@genetics.washington.edu (IP No. 128.95.12.41) Dept. of Genetics, Univ. of Washington, Box 357360, Seattle, WA 98195-7360 USA From jonmac@u.washington.edu Thu Feb 27 07:17:35 PST 1997 Article: 29 of uwash.class.genet453 Path: news.u.washington.edu!root From: jonmac@u.washington.edu (Jon McBride) Newsgroups: uwash.class.genet453 Subject: Re: migration Date: Mon, 24 Feb 1997 05:35:22 GMT Organization: University of Washington Lines: 26 Message-ID: <331227a5.344421@news.u.washington.edu> References: <32fe224b.1304965@news.u.washington.edu> <5dmf48$4g2@nntp3.u.washington.edu> NNTP-Posting-Host: cs232-10.student.washington.edu Mime-Version: 1.0 Content-Type: text/plain; charset=us-ascii Content-Transfer-Encoding: 7bit X-Newsreader: Forte Agent .99g/32.339 On 10 Feb 1997 06:27:20 GMT, joe@evolution.genetics.washington.edu (Joe Felsenstein) wrote: >In article <32fe224b.1304965@news.u.washington.edu>, >Jon McBride wrote: >>So, in a way, one could >>think of migration as a restriction that is placed on a population of >>individuals to limit the extent that they breed (m = 1-r) and, in >>effect, creating subpopulations. Then one would expect, as I observed >>in the simulation, the differentiation of the simulated populations to >>be small. > >Well, you would expect that, but I don't find it any clearer than just >thinking about migration. But 30 years in the field may have warped >my idea of what is clear ... > You're right. Just thinking about migration is easier and more clear, but the only way to truly grasp a concept is to be able to apply the information one already knows to a new explanation. The more a concept is processed by the mind, and the more aspects of that concept one considers, the clearer it actually is. Jon McBride jonmac@u.washigton.edu From jonmac@u.washington.edu Thu Feb 27 07:18:24 PST 1997 Article: 30 of uwash.class.genet453 Path: news.u.washington.edu!root From: jonmac@u.washington.edu (Jon McBride) Newsgroups: uwash.class.genet453 Subject: phylogenetic trees Date: Mon, 24 Feb 1997 05:41:50 GMT Organization: University of Washington Lines: 15 Message-ID: <331328a1.596429@news.u.washington.edu> NNTP-Posting-Host: cs232-10.student.washington.edu Mime-Version: 1.0 Content-Type: text/plain; charset=us-ascii Content-Transfer-Encoding: 7bit X-Newsreader: Forte Agent .99g/32.339 This may be a silly question, but I will ask it anyway... Last Wednesday when Dr. Rodrigo was lecturing about phylogenetic trees he defined a clade as a group of taxa who exclusively share a common ancestor. By that definition, clades have varying degrees of specificity. It seems (in principle) that one could define an entire phylogenetic tree as a clade because in order to be in a tree, all of the organisms must have shared a common ancestor at one point. So I guess my question is: do clades apply to all sections of a phylogenetic tree, or just to the terminal branches as he illustrated in his example? Jon McBride jonmac@u.washigton.edu From joe@evolution.genetics.washington.edu Thu Feb 27 07:18:38 PST 1997 Article: 31 of uwash.class.genet453 Path: news.u.washington.edu!evolution.genetics.washington.edu!joe From: joe@evolution.genetics.washington.edu (Joe Felsenstein) Newsgroups: uwash.class.genet453 Subject: Re: phylogenetic trees Date: 24 Feb 1997 18:09:36 GMT Organization: University of Washington Genetics Lines: 23 Message-ID: <5eslh0$oif@nntp3.u.washington.edu> References: <331328a1.596429@news.u.washington.edu> NNTP-Posting-Host: evolution.genetics.washington.edu Summary: Clades apply to all In article <331328a1.596429@news.u.washington.edu>, Jon McBride wrote: >Last Wednesday when Dr. Rodrigo was lecturing about phylogenetic trees >he defined a clade as a group of taxa who exclusively share a common >ancestor. By that definition, clades have varying degrees of >specificity. It seems (in principle) that one could define an entire >phylogenetic tree as a clade because in order to be in a tree, all of >the organisms must have shared a common ancestor at one point. So I >guess my question is: do clades apply to all sections of a >phylogenetic tree, or just to the terminal branches as he illustrated >in his example? A clade is a part of a phylogeny consisting of an ancestor and all its descendants. Thus the descendants of the first vertebrate to become terrestrial are a clade. But if you leave out the bats, birds, whales, say, then the remainder isn't a clade. An entire phylogeny is a clade. It isn't a notion just confined to terminal branches. -- Joe Felsenstein joe@genetics.washington.edu (IP No. 128.95.12.41) Dept. of Genetics, Univ. of Washington, Box 357360, Seattle, WA 98195-7360 USA From jonmac@u.washington.edu Fri Mar 28 06:20:47 PST 1997 Article: 32 of uwash.class.genet453 Path: news.u.washington.edu!root From: jonmac@u.washington.edu (Jon McBride) Newsgroups: uwash.class.genet453 Subject: horses and donkeys Date: Tue, 11 Mar 1997 01:37:07 GMT Organization: University of Washington Lines: 14 Message-ID: <3324b530.22016375@news.u.washington.edu> NNTP-Posting-Host: cs208-19.student.washington.edu Mime-Version: 1.0 Content-Type: text/plain; charset=us-ascii Content-Transfer-Encoding: 7bit X-Newsreader: Forte Agent .99g/32.339 O.K., I have a question about what yo where talking about last Friday in class. I was thinking last weekend about what you had said about trans-species offspring. For example, a horse and a donkey produce a mule (I think that is how it goes anyway) that is unable to reproduce. Is the reason a mule is sterile because it is unlikely that a mule's gametes will get a least one copy of each chromosome since after chromosome segregation, there will most likely be duplication/deficiency problems? I was trying to think of a real life case to illustrate the point you were trying to make, was I successful or is this just a coincidence? Jon McBride jonmac@u.washigton.edu From joe@evolution.genetics.washington.edu Fri Mar 28 06:21:02 PST 1997 Article: 33 of uwash.class.genet453 Path: news.u.washington.edu!evolution.genetics.washington.edu!joe From: joe@evolution.genetics.washington.edu (Joe Felsenstein) Newsgroups: uwash.class.genet453 Subject: Re: horses and donkeys Date: 12 Mar 1997 17:53:25 GMT Organization: University of Washington Genetics Lines: 28 Message-ID: <5g6qil$e0a@nntp3.u.washington.edu> References: <3324b530.22016375@news.u.washington.edu> NNTP-Posting-Host: evolution.genetics.washington.edu Summary: Maybe ... In article <3324b530.22016375@news.u.washington.edu>, Jon McBride wrote: >Is the reason a mule is sterile because it is unlikely that a mule's >gametes will get a least one copy of each chromosome since after >chromosome segregation, there will most likely be >duplication/deficiency problems? I used to hear this asserted regularly. Apparently donkeys have 62 chromosomes (diploid number) and horses have 64. The chromosomes differ in numerous ways. People used to say that this was the reason for the sterility of the mule and the hinny (one is donkey male x horse female, the other is the other way 'round). But more recently I dimly recall having heard that this is not the reason. The reference that seems to be the one to read is: Chandley, A. C., R. Jones, H. M. Dott, W. R. Allen, and R. V. Short. 1974. Meiosis in interspecific equine hybrids, I: The male mule (E. asinus X E. caballus) and hinny (E. caballus X E. asinus). Cytogenetics and Cell Genetics 13: 330-341. If you get a chance to look at it (it should be in Health Sciences Library) let me know what it says on this point. Recent textbooks avoid the earlier claim, and I'm a bit swamped and unable to take time to go read this. -- Joe Felsenstein joe@genetics.washington.edu (IP No. 128.95.12.41) Dept. of Genetics, Univ. of Washington, Box 357360, Seattle, WA 98195-7360 USA From joe@evolution.genetics.washington.edu Fri Mar 28 06:21:21 PST 1997 Article: 34 of uwash.class.genet453 Path: news.u.washington.edu!evolution.genetics.washington.edu!joe From: joe@evolution.genetics.washington.edu (Joe Felsenstein) Newsgroups: uwash.class.genet453 Subject: Review session and final exam Date: 12 Mar 1997 17:55:27 GMT Organization: University of Washington Genetics Lines: 9 Message-ID: <5g6qmf$e12@nntp3.u.washington.edu> NNTP-Posting-Host: evolution.genetics.washington.edu Summary: When they are The review session will be this Friday, March 14, in J280 (the usual lecture room) at 3:30-4:30. The final exam will, as previously announced, be in J280 at 2:30-4:30 on Wednesday, March 19. -- Joe Felsenstein joe@genetics.washington.edu (IP No. 128.95.12.41) Dept. of Genetics, Univ. of Washington, Box 357360, Seattle, WA 98195-7360 USA From joe@evolution.genetics.washington.edu Fri Mar 28 06:21:57 PST 1997 Article: 35 of uwash.class.genet453 Path: news.u.washington.edu!evolution.genetics.washington.edu!joe From: joe@evolution.genetics.washington.edu (Joe Felsenstein) Newsgroups: uwash.class.genet453 Subject: Picking up your exam Date: 21 Mar 1997 18:07:03 GMT Organization: University of Washington Genetics Lines: 9 Message-ID: <5guio7$9i9@nntp3.u.washington.edu> NNTP-Posting-Host: evolution.genetics.washington.edu Summary: Monday in J205 We will have the exams available for pickup by Monday. They will be in J205 HSB (the Genetics Department Office). I will post and put on the web site the grade distribution. Am thinking about what to do about a Key to the exam. ---- Joe Felsenstein joe@genetics.washington.edu (IP No. 128.95.12.41) Dept. of Genetics, Univ. of Washington, Box 357360, Seattle, WA 98195-7360 USA From joe@evolution.genetics.washington.edu Fri Mar 28 06:22:19 PST 1997 Article: 36 of uwash.class.genet453 Path: news.u.washington.edu!evolution.genetics.washington.edu!joe From: joe@evolution.genetics.washington.edu (Joe Felsenstein) Newsgroups: uwash.class.genet453 Subject: Key for exam Date: 24 Mar 1997 20:18:03 GMT Organization: University of Washington Genetics Lines: 7 Message-ID: <5h6nhr$i0@nntp3.u.washington.edu> NNTP-Posting-Host: evolution.genetics.washington.edu Summary: in J205, you can copy A rudimentary key for the final exam is available in J205 HSB (the Genetics Office) from the secretary at the front desk, Bill, who will allow you to copy it. There wasn't enough bulletin board space to post it. -- Joe Felsenstein joe@genetics.washington.edu (IP No. 128.95.12.41) Dept. of Genetics, Univ. of Washington, Box 357360, Seattle, WA 98195-7360 USA