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it won't be long before the entire business of publishing scholarly works ... will be drastically altered given the web and internet. the notion of reviewed submissions will be outmoded (for good or for bad) soon .... and papers etc. will merely be posted to the web ... for all to use/read/take/absorb ... the day of the printed/referred journal is rapidly limited ... At 04:57 PM 12/18/96 -0500, you wrote: >Dear list members: > >Ron LaPorte at Univ. of Pittsburgh posted this on the epidemio-l list server >at Univ. of Montreal and asked that it be forwarded to other lists. The >posting describes a Web home page that is addressing the challenges journal >houses face with regard to publishing on the internet. In view of Ron's >request, I have forwarded it to the following list servers: > >icrher@listserv.bcm.tmc.edu >DOSE-NET@orau.gov >MEDPHYS@CMS.CC.WAYNE.EDU >cdn-nucl-l@listserv.cis.mcmaster.ca >radsafe@romulus.ehs.uiuc.edu >EPIWORLD@UNIVSCVM.CSD.SCAROLINA.EDU >stat-l@vm1.mcgill.ca > >Please don't send it on to these lists. > >Leif E. Peterson, Ph.D. >ICRHER List Administrator (icrher@listserv.bcm.tmc.edu) >International Consortium for Research on Health Effects of Radiation >Baylor College of Medicine >Houston, Texas >peterson@bcm.tmc.edu > > >Message follows: >----------------------------------------- >Date: Tue, 17 Dec 1996 18:31:20 -0400 (EDT) >From: "Ronald E. LaPorte from Pittsburgh"Return to Top>To: epidemio-l@CC.UMontreal.CA >Subject: Re: EPIDEMIO-L digest 804 >Message-ID: <01ID4K8JA5TU936DOO@vms.cis.pitt.edu> > > >Dec. 1996 > > > >High Noon for Biomedical Journals > >Scientists from the Global Health Network >(www.pitt.edu/HOME/GHNet/GHNet.html) predict that within >5 years most scientists will move their intellectual properties >to the Internet. This will spell the demise of most paper >journals as we know them. In two recent communications in >the British Medical Journal they indicated that an Internet >based system would be much more powerful and available to >scientists then journals. Moreover, they are questioning the >current copyright practice of the journals as this inhibits the >use of the Internet for posting communications. A major >problem, however, is that little is known about how best to >present research communications on the Internet. In their >web site (www.pitt.edu/HOME/GHNet/publications/assassin/), >an experiment is being conducted where a research >communication called Scientists Assassinate Journals is >presented in English, Spanish, Portuguese and Japanese. >This is presented in a lay version, scientific version, or an >editor version. In addition, it is presented in a "hypertext >comic book form", all include sound. Within each version >there are considerable opportunities to provide constructive >comments concerning the presentation or content. > >We encourage scientists, editors, and lay people from all >walks of life to come to our site and comment. In this >manner, we will have data from the scientific community as to >how best to present scientific research communications. We >would suggest that you forward this to your friends and to list >servers and news groups as this affects the total scientific >community, therefore, the more input the better. > >Ronald LaPorte, Ph.D. >Deborah Aaron, Ph.D. >Akira Sekikawa, M.D. >Ingrid Libman, M.D., Ph.D. >Benjamin Acosta, M.D. >Lucia Iochida, Ph.D. >Eugene Boostrom, M.D. >Anthony Villasenor, B.S. >Amy Brenen, B.S. > >
Hello, If the entries of a matrix W follow the inverse Wishart distribution with scale matrix S and degrees of freedom v, what is the marginal distribution of a diagonal element w(i,i) ? what is the distribution of w(i,i) conditinal on the rest of the entries in W? Thank you in advance for any hints! Andreas HoferReturn to Top
+-------------------+-------------------------------------------------------+ | | ****** ******* ** | | *** European | * ** * ** * | | * Course | ** ** **** ***** ****** ** * ****** *** | | ** In | ** *** ** ** ** ** ** **** ** ** ** | | * Tropical | ** ** ** ** ** ** ** * ** ** ** | | *** Epidemiology | ** ** ** ** ****** ** * ****** ** | | | **** ** ***** ** ******* ** **** | | November '96 # 3 | ** ** | +-------------------+-------------------------------------------------------+ | Newsletter of the Network of the European Course in Tropical Epidemiology | +---------------------------------------------------------------------------+ Report from the 1996 Course in London -=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=- Twenty-seven students from Angola, Brazil, Gambia, Ghana, Georgia (CIS), Holland, India, Japan, Kenya, Malawi, Nigeria, Sudan, Sweden, Tanzania, Thailand, Tunisia, Uganda, United Kingdom, United States, Yemen, and Zimbabwe came together in August for the Fifteenth European Course in Tropical Epidemiology (ECTE) hosted by the London School of Hygiene and Tropical Medicine. Overall evaluation of the course was very good, with a mean score for the participants general judgement being 7.3 out of 9.0. The computer sessions were very popular - the new all day format worked extremely well. The group-work sessions were also well received. As in previous years, the more experienced statistics group was more difficult to please. Changes for 1997 -=-=-=-=-=-=-=-= On the basis of the course evaluation, the course steering committee approved several changes to the course format that will be phased in over the coming years. More sessions will be organised as larger teaching blocks. The risk sessions, which could easily take a whole day but are rushed in the current timetable, were identified as a suitable module for this new approach. An applied statistical methods module will be available as a group-work option. This should satisfy participants who would like to see some advanced statistics in the course. The other group-work sessions will remain at the introductory level but more options may be added (including maternal and child health, sexual and reproductive health, and epidemiology in emergency situations). The current double-session on nutritional surveillance sessions will be dropped and replaced by a nutritional epidemiology group work option. Sessions on health service research, epidemiology of chronic disease, and a highly practical introduction to epidemiology session will also be added. Some of these changes will be seen in the 1997 course which will be hosted by the Institute of Tropical Medicine in Heidelberg, Germany. For further information about the 1997 course contact: Ms Anke Nitschke Department of Tropical Hygiene and Public Health Im Neuenheimer Feld 324 D-69120 Heidelberg Germany Tel: +49 6221 564905 Fax: +49 6221 564918 E-mail: anke.nitschke@urz.uni-heidelberg.de The Future -=-=-=-=-= The future for the ECTE is bright. Student numbers remain at viable levels (even at the traditionally low course fees). Course evaluations also remain good. The search is on for a venue for the 1998, 1999, and 2000 courses. Potential venues include Portugal, Holland, and Wales. Efforts will also be made to find a suitable venue in Eastern Europe. CDC announce a new version of EpiInfo =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= The latest version of the public domain medical statistics package EpiInfo (v6.04a) has just been released by the Epidemiological Program Office of the Centres for Disease Control. Copies of the program are available on the Internet and from Brixton Books. EpiInfo is now supported by an Internet mailing list. You can subscribe to this list or download a copy of the latest version from: http://mkn.co.uk/help/extra/people/brixton_books Work has started on a WindowsTM version of the program which should be available by Summer 1997. More information will appear in TropEpi when a review copy is available. Personals -=-=-=-=- It is with deep regret that we report the death of Nicola Dollimore who died in a caving accident this summer. Nicola was a motivating force for the course and had taught and developed the statistics modules over many years. She will be sadly missed by all who knew her. ECTE 1997 -=-=-=-=- The 16th ECTE will be held from the 8th - 20th September 1997 and will be organised and hosted by the Institute of Tropical Medicine in Heidelberg, Germany in collaboration with: DeptEpidemiology and Community Medicine Universtity of Antwerp, Belgium Institute of Tropical Medicine, Antwerp, Belgium National Institute for Public Health, Prague, Czech Republic Bureau for Topical Medicine and Hygiene, Copenhagen, Denmark London School of Hygiene and Tropical Medicine, London, UK GTZ GmbH, Eschborn, Germany Seccion de Medicina Tropical, Hospital Clinic, Barcelona, Spain Nordic School of Public Health, Göteborg, Sweden Swiss Tropical Institute, Basel, Switzerland Liverpool School of Tropical Medicine, Liverpool, UK Brixton Books / Brixton Health, Llanidloes, Wales The European Course in Tropical Epidemiology -=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= The European Course in Tropical Epidemiology is a collaborative venture between various European institutes of tropical medicine and private sector organisations. It is held annually in a different location. This intensive introductory course in epidemiology is intended for physicians, nurses, health programme managers, health administrators, NGO field workers, and other persons with a professional interest in health in tropical countries. The course provides participants with basic skills in the epidemiological assessment of health problems and service priorities and in the planning and execution of field studies. Emphasis is placed on methodology, the practical application of epidemiological tools in developing countries, the interpretation of data, and the reporting of field studies. This is an introductory level course and is appropriate for those with no formal training in epidemiology or statistics. The course is very intensive. Applicants should have a good command of English. A certificate of attendance will be awarded to those completing the course. Outline of the program -=-=-=-=-=-=-=-=-=-=-= Teaching will include lectures, seminars, practical exercises, and group-work. Use will be made of the epidemiological software package EpiInfo to illustrate and support teaching. The following subjects will be included: Basic epidemiology of infectious diseases Basic epidemiology of non-infectious diseases Risk estimation, risk groups, risk factors, and risk markers Screening tests and screening programmes Epidemics and outbreaks Nutritional epidemiology Qualitative methods in epidemiology Sampling and sample size calculation Survey design and organisation Questionnaire design Data management Basic medical statistics using computers Textbooks and course materials A course manual providing comprehensive study material will be given to participants at the start of the course. For those interested in preparatory reading the following texts are recommended: Epidemiology in Medicine, Hennekens CH, Buring JE, Little Brown, 1987 Essentials of Medical Statistics, Kirkwood BR, Blackwell, 1988 Course fee The total course fee is DM2000. This includes participation in the course, course material, incidental refreshments, and reception but does not include travel costs, accommodation, or meals. The full course fee is payable on notification of acceptance on the course. Admission will be confirmed when payment is received. Since the number of places is limited, priority will be given to early applicants. Applicants from developing countries are advised to contact sponsoring organisations immediately. Accommodation -=-=-=-=-=-=- Accommodation is available at a hall of residence close to the Department, which offers self-catering facilities. The price will be approximately DM250 for the two weeks and does not include breakfast. Lunch is available from the University canteen (costing around DM5). Participants should arrive in Heidelberg on Sunday 7th September. Heidelberg is situated 70km south of Frankfurt (the nearest main international airport) and can be reached in 1-2 hours by either train or bus. Applying for a place on the Course -=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= If you want to apply to attend the 16th European Course in Tropical Epidemiology you should contcat: Ms Anke Nitschke Department of Tropical Hygiene and Public Health Im Neuenheimer Feld 324 D-69120 Heidelberg Germany Tel: +49 6221 564905 Fax: +49 6221 564918 E-mail: anke.nitschke@urz.uni-heidelberg.de -- Mark MyattReturn to Top
Dennis RobertsReturn to Topwrites: >DOES A SIMPLE REGRESSION ANALYSIS ... REQUIRE A NORMALLY DISTRIBUTED >DEPENDENT MEASURE? WHAT ABOUT THE INDEPENDENT VARIABLE? >At 10:46 PM 12/17/96 EST, you wrote: >> We need to do regression analysis with RATIO (e.g., cost/benefit) as a >>dependent variable, but I was told that I might violate normal distribution >>assumption if I do so. Any comments, suggestions? Assume we are discussion ordinary least squares regression. 1. Parameter estimates are least squares regardless of the parent distribution. 2. How useful those estimates are is another issue. 3. In the absense of large samples, approximate normality enables the distribution of the test statistics under the null hypothesis to be known. 4. "Large" enough samples obviate the need to know the parent distribution. 5. How large "large" enough is depends on how badly the population is distributed. 6. The randomness of the sampling and the independence of the observations are of key importance. -- --(Signature) Robert M. Hamer hamer@rci.rutgers.edu 908 235 4218 Do not send me unsolicited email advertisements. I have never and will never buy. I will complain to your postmaster. "Mit der Dummheit kaempfen Goetter selbst vergebens" -- Schiller
> it won't be long before the entire business of publishing scholarly wor= ks > ... will be drastically altered given the web and internet. the notion = of > reviewed submissions will be outmoded (for good or for bad) soon .... = and > papers etc. will merely be posted to the web ... for all to > use/read/take/absorb ... > > the day of the printed/referred journal is rapidly limited ... There will still be a place for reviewed "journals" or their equivalent = on the web: otherwise we'd all overwhelmed. A reviewed electroinc journal will sift out the better work= , and still have all the advantages of the web (speed, links, animations etc.). Looking forward to it. ----------------------------------------------------------------- barryh@agb.com.au Barry Haworth, Sampling Statistician, AGB McNair PO Box 507, North Sydney 2059, AUSTRALIA (02) 9911 7200 (ph) (02) 9959 4947 (fax) http://www.agb.com.auReturn to Top
On Mon, 16 Dec 1996 17:34:09 -0500, "Joseph K. Lyou"Return to Topwrote: >I want to analyze whether there is a significant trend over time in the >annual failure rate of a product. I have 20 years of measurements (i.e., n = >20). As I understand it, an ordinary regression analysis would be >inappropriate because the residuals are not independent (i.e., the error >associated with a failure rate for 1974 is more highly correlated with the >1975 failure rate than the 1994 failure rate). Is it appropriate to simply >divide the data into two groups (the 1st 10 years vs. the 2nd 10 years) and >do a between-groups ANOVA? Or is there some other (better) way to analyze >these data? > >Should anyone be so inclined as to do the analysis, here are the data: > >Year Failure Rate >1974 3.3 >1975 2.5 >1976 2.7 >1977 2.4 >1978 5.7 >1979 3.2 >1980 1.6 >1981 5.2 >1982 2.8 >1983 2.4 >1984 2.7 >1985 1.3 >1986 4.5 >1987 4.5 >1988 1.4 >1989 3.6 >1990 1.5 >1991 1.4 >1992 1.6 >1993 1.6 i would first of all try to apply the (qualitative) cox-stuart trend test. alex ======================================== DI Alexander Schatten Institute for General Chemistry University of Technology Vienna email: aschatt@fbch.tuwien.ac.at URL: http://echm10.tuwien.ac.at/inst/as Tel.: +43 1 914-29-84 ========================================
Dennis Roberts writes: >it won't be long before the entire business of publishing scholarly works >... will be drastically altered given the web and internet. the notion of >reviewed submissions will be outmoded (for good or for bad) soon .... and >papers etc. will merely be posted to the web ... for all to >use/read/take/absorb ... > >the day of the printed/referred journal is rapidly limited ... While dreamy eyed predictions of the future are fun, reality has a way of ruining things. Just like how I get a busy signal every time I try to use my America Online account. First, there is nothing inherent about web publications that prevent the use of peer review, just like there is nothing inherent in paper publications that mandate the use of peer review. Second, Internet will no more replace paper publications any more than television replaced movies and theater. Both Internet and paper publications are likely to co-exist for a long time. Steve Simon, ssimon@cmh.edu, Standard Disclaimer. -------------------==== Posted via Deja News ====----------------------- http://www.dejanews.com/ Search, Read, Post to UsenetReturn to Top
* * * * Peace * * * * * * * * * to * * * * * * * * * * * * * * One and All, * * * * * * * * * * * * * * * * Now and in the * * * * * * * * * * * * * New Year!! * * * * * * * * * * * * * * * * * * * * * * * * WBW 1996 ______________________________________________________________________________ William B. Ware, Professor and Chair Educational Psychology CB# 3500 EMAIL: wbware@unc.edu University of North Carolina PHONE: (919)-966-5266 Chapel Hill, NC 27599-3500 FAX: (919)-962-1533 URL:http://www.unc.edu/~wbware/ ______________________________________________________________________________Return to Top
Hi, If anyone is researching on material like PAR models and periodic integration and cointegration, I would appreciate some help with certain problems I'm having. Please reply by email. Many thanks. Kenneth.Return to Top
I've been exposed to the three Erlang models (A, B or Poisson, C) where blocked telephone calls are cleared, delayed or held. Now I'm looking at modeling tasks of a more complex nature such as writing 100 C++ subroutines or building 100 regression models. If each regression model averaged 3 hours to build, I could use the Poisson distribution to find out how many data analysts I would need to ensure only one chance in 20 that a model building request would be "blocked", if we experience a demand of 5 model building requests per day. BUT setup of telephone calls is usually quite quick and almost NEVER interrupted, while a task which averages 3 hours will almost ALWAWS be interrupted, at least once, so -- QUESTION: is there a model which accounts for task interruptions, or should I just ignore them and use the Poisson? The problem is complicated by the fact that some interruptions (like LUNCH) make the analyst unavailable, while others (need for a corrected dataset) actually make the analyst available to build other models. Just think -- if there's a solution to this, we'll be able to schedule data analysts for split shifts just like we now do with telephone operators or counter people at McDonalds -- HEY -- there could be a: "MODELS-R-US - Regression Models while you Wait - Your model in 3 hours or IT'S FREE" Well Howell (whowell@superlink.net)Return to Top
In articleReturn to Top, Barry Haworth writes: |> > it won't be long before the entire business of publishing |> > scholarly works ... will be drastically altered given the web and |> > internet. the notion of reviewed submissions will be outmoded |> > (for good or for bad) soon .... and papers etc. will merely be |> > posted to the web ... for all to use/read/take/absorb ... |> > |> > the day of the printed/referred journal is rapidly limited ... |> |> There will still be a place for reviewed "journals" or their |> equivalent on the web: otherwise we'd all overwhelmed. A reviewed |> electroinc journal will sift out the better work, and still have |> all the advantages of the web (speed, links, animations etc.). Why not just let links take the place of reviewing? After all, what is a review except the sanction of a recognized authority? If I recognized you as an authority on statistics, I'd just go to your home page and examine the links to papers you'd read recently and approved of. |> Looking forward to it. Ditto. -- Randy Tobias SAS Institute Inc. sasrdt@unx.sas.com (919) 677-8000 x7933 SAS Campus Dr. us024621@interramp.com (919) 677-8123 (Fax) Cary, NC 27513-2414 Faith, faith is an island in the setting sun. But proof, yes: proof is the bottom line for everyone. -- Paul Simon
makes sense to me but ... the powers to be for promotion and tenure seem to want MORE than that. personally ... since the appearance in a good journal does not assure that the article/study was good ... i prefer to make my work available .. and let those who access it decide if it is useful/good or not. the acceptance by a journal does not make it so ... but we have come to rely SO heavily on its appearance in a decent journal being THE proof of worth ... i think we have forgotten that intelligent readers can figure that out on their own .. At 04:00 PM 12/19/96 GMT, you wrote: >In article >Return to Top, Barry >Haworth writes: >|> > it won't be long before the entire business of publishing >|> > scholarly works ... will be drastically altered given the web and >|> > internet. the notion of reviewed submissions will be outmoded >|> > (for good or for bad) soon .... and papers etc. will merely be >|> > posted to the web ... for all to use/read/take/absorb ... >|> > >|> > the day of the printed/referred journal is rapidly limited ... >|> >|> There will still be a place for reviewed "journals" or their >|> equivalent on the web: otherwise we'd all overwhelmed. A reviewed >|> electroinc journal will sift out the better work, and still have >|> all the advantages of the web (speed, links, animations etc.). > >Why not just let links take the place of reviewing? After all, what >is a review except the sanction of a recognized authority? If I >recognized you as an authority on statistics, I'd just go to your home >page and examine the links to papers you'd read recently and approved >of. > >|> Looking forward to it. > >Ditto. > > >-- >Randy Tobias SAS Institute Inc. sasrdt@unx.sas.com >(919) 677-8000 x7933 SAS Campus Dr. us024621@interramp.com >(919) 677-8123 (Fax) Cary, NC 27513-2414 > > Faith, faith is an island in the setting sun. > But proof, yes: proof is the bottom line for everyone. > -- Paul Simon > > =========================== Dennis Roberts, Professor EdPsy !!! GO NITTANY LIONS !!! 208 Cedar, Penn State, University Park, PA 16802 AC 814-863-2401 WEB (personal) http://www2.ed.psu.edu/espse/staff/droberts/drober~1.htm
D.C.Lee (DLEE@cms.cc.wayne.edu) wrote: : Hello All, : : I am seeking to develop a predictive model of a particular : phisiological parameter(response variable) using to other : phisiological parameters as predictor variables. Of the : response variable, or parameter, I am interested in events : which occur only 0 to 5 times during a four hour test run.The : event lasts only five or ten minutes as a spike and has a : relatively quick decay. The response variable is nearly -- 5 minutes plus the surrounding hour, taken 5 times, is more than the 4-hour test. But if you have a bunch of 0-0-0 sort of data, it will contribute nothing to the useful prediction, once you have accounted for a LITTLE of it. It might make your R-squared look bigger, by predicting a lot more zero-scores, even though the error (computed residuals) are getting bigger for the peaks that you are really interested in. If you are trying to *predict* a "spike", is there ANY purpose in looking at the data for the next half hour? Do your spikes ever double up that way? Deciding on transformations is something that you do while looking at the data with multiple spikes for a person. Does a transformation preserve (or even, enhance) the similarities of the spikes for one person? If the data for one person looks 'typical' for that PERSON, then the proper analysis would create scores or parameters of some kind, by PERSON, and then do your eventual testing across N=20 people. You might do an analysis controlling for Subject, but I think you would never drop the dummy-variables for Subject. That seems too much like double-counting your sample. Rich Ulrich, biostatistician wpilib+@pitt.edu Western Psychiatric Inst. and Clinic Univ. of PittsburghReturn to Top
Peter Midford (pmidford@students.wisc.edu) wrote: : I'm wondering if it is possible to calculate power values (1 - Beta) : for one or all of the common contingency table tests (e.g. chi-square, G, : Fisher's exact). -- Most any text, for Pearson's contingency table chisquare. Try Cohen, "Statistical Power Analysis for the Behavioral Sciences". Rich Ulrich, wpilib+@pitt.eduReturn to Top
Many thanks for everybody's input. It seems a statistician is a necessity (as I expected) and I'll have to wait. I'm sorry I glossed over the study's structure, as I underestimated the medical knowledge present in this group. All patients in the study were treated by 8 doctors of the Helicopter Emergency Medical service working to strict guidelines, and most details of the prehospital phase are available for analysis. RTS, and other physiological scores are taken from the first readings made on scene (around 10 minutes into the incident), and so should be unaffected by time spent on scene). All medical interventions have been recorded, along with details of extrication etc. Basically a rough over view of the data seems to suggest that time spent on scene is not correlated with survival, ITU stay, Hospital Stay or functional independence at 12 months. But obviously a meticulous statistical analysis will need to be performed to confirm or deny this. Once again many thanks for your input, and I am impressed by the knowledge displayed. -- __________________________________________________ Dr. Karim Brohi BSc FRCS FRCA Trauma & Critical Care Unit, Royal London Hospital Mailto:karim@trauma.org http://www.trauma.org/Return to Top
We are testing a new lab test versus the standard test. We will calculate sensitivity and specificity of the new test. How do I determine the sample size needed to have valid results? Susan Adlis adliss@found.hsmnet.comReturn to Top
what do you mean by "valid"??? if you are asking ... to find out if there is really a true difference in effect ... but, we know of course that the two cannot have the same IDENTICAL impact. so ... you must try to rationally decide on what SIZE of an impact you would consider to be important ... AT A MINIUM. the question you have asked on the surface would seem to have a simple answer but .. it does not. At 01:46 PM 12/19/96 PST, you wrote: >We are testing a new lab test versus the standard test. We will calculate >sensitivity and specificity of the new test. How do I determine the sample >size needed to have valid results? > >Susan Adlis >adliss@found.hsmnet.com > > =========================== Dennis Roberts, Professor EdPsy !!! GO NITTANY LIONS !!! 208 Cedar, Penn State, University Park, PA 16802 AC 814-863-2401 WEB (personal) http://www2.ed.psu.edu/espse/staff/droberts/drober~1.htmReturn to Top
nakhob@mat.ulaval.ca (Renaud Langis) writes: >On Fri, 13 Dec 1996 00:07:22 -0500, Ya-Fen LoReturn to Top>wrote: >>Is it possible to perform tests of simple effects >>(as defined in APPLIED STATISTICS by HINKEL/WIERSMA/JURS) >>in SAS ? I am using the following setup Yes. >You can use the TEST statement in proc GLM. May be also in proc ANOVA. Do you >simply want to know if an effect is significant? if so, just check the ANOVA >table. That is not what the original question asked. That person wants to contrast levels of one effect at specific levels of the other effect. One has to do that with CONTRAST or ESTIMATE statements. >I suppose this is just a typing error but CLASSES should be written CLASS. Actually, CLASS works just fine. It is one of the several alternative forms of the statement available. -- --(Signature) Robert M. Hamer hamer@rci.rutgers.edu 908 235 4218 Do not send me unsolicited email advertisements. I have never and will never buy. I will complain to your postmaster. "Mit der Dummheit kaempfen Goetter selbst vergebens" -- Schiller
Richard F Ulrich (wpilib+@pitt.edu) wrote: : Barry Haworth (barryh@AGB.COM.AU) wrote: : << concerning the sampling of 300 out of 3000 ... >> : : :" Taking a sample of a sample is perfectly appropriate, so long as : the second sample is drawn in a sensible way (a random sample of all : the original responses, for example)" (The 3 lines immediately above are from my reply.) : : -- Please, if you have to analyze the 300, then draw them : SYSTEMATICALLY rather than randomly. For instance, it is VERY OFTEN : useful to know if the early (fast?) respondents were different : from those whose forms came in last. (In mortality followups, : one looks to see if the causes of death are different for those : whose records were hardest to find - found by 'only one method' : or found only by persistent checking.) : In the survey literature, systematic sampling refers to taking every k-th observation (say, every 10th one in this case). Provided that the first one is randomly selected (random start), this is a form of random or probability sampling (not simple random sampling). I was really trying to guard against taking a "convenience" sample -- these can lead to big trouble. I think we have here a difference in terminology more than anything else. : You might draw 100 early+middle+late for your 300, so you could : compare. Big changes across the strata suggest a big chance : that your Unsampled cases are even more different than early vs late. : Fine. A stratified random sample would do nicely. -- Michael P. Cohen home phone 202-232-4651 1615 Q Street NW #T-1 office phone 202-219-1917 Washington, DC 20009-6331 office fax 202-219-2061 mcohen@cpcug.orgReturn to Top
************* 1997 Course Announcement ********* MODERN REGRESSION AND CLASSIFICATION Waikiki, Hawaii: February 17-18, 1997 ************************************************* A two-day course on widely applicable statistical methods for modeling and prediction, featuring Professor Trevor Hastie and Professor Robert Tibshirani Stanford University University of Toronto This course was offered and enthusiastically attended at five different locations in the USA in 1996. This two day course covers modern tools for statistical prediction and classification. We start from square one, with a review of linear techniques for regression and classification, and then take attendees through a tour of: o Flexible regression techniques o Classification and regression trees o Neural networks o Projection pursuit regression o Nearest Neighbor methods o Learning vector quantization o Wavelets o Bootstrap and cross-validation We will also illustrate software tools for implementing the methods. Our objective is to provide attendees with the background and knowledge necessary to apply these modern tools to solve their own real-world problems. The course is geared for: o Statisticians o Financial analysts o Industrial managers o Medical and Quantitative researchers o Scientists o others interested in prediction and classification Attendees should have an undergraduate degree in a quantitative field, or have knowledge and experience working in such a field. PRICE: $750 per attendee if received by January 15, 1997. Full time registered students receive a 40% discount. Attendance is limited to the first 60 applicants, so sign up soon! These courses fill up quickly. TO REGISTER: Fill in and return the form appended. For more details on the course and the instructors: o point your web browser to: http://stat.stanford.edu/~trevor/mrc.html OR send a request by o FAX to Prof. T. Hastie at (415) 326-0854, OR o email to trevor@stat.stanford.edu <----------------------------- Cut Here -------------------------------> Please print, and fill in the hard copy to return by mail or FAX REGISTRATION FORM Modern Regression and Classification Monday, February 17 and Tuesday, February 18, 1997. Hilton Hawaiian Village, Waikiki Beach, Honolulu, Hawaii. Name ___________________________________________________ Last First Middle Firm or Institution ______________________________________ Standard Registration ____ Student Registration ____ Mailing Address (for receipt) _________________________ __________________________________________________________ __________________________________________________________ __________________________________________________________ Country Phone FAX __________________________________________________________ email address __________________________________________ _______________ Credit card # (if payment by credit card) Expiration Date (Lunch preference - tick as appropriate): ___ Vegetarian ___ Non-Vegetarian Fee payment can be made by MONEY ORDER , PERSONAL CHECK, or CREDIT CARD (Mastercard or Visa.) For checks and money orders: all amounts are given in US dollar figures. Make fee payable to Prof. T. Hastie. Mail it, together with this completed Registration Form to: Prof. T. Hastie 538 Campus Drive Stanford CA 94305 USA For payment by credit card, include credit card details above, and mail to above address, or else FAX form to 415-326-0854 For further information, contact: Trevor Hastie Stanford University Tel. or FAX: 415-326-0854 e-mail: trevor@stat.stanford.edu. http://stat.stanford.edu/~trevor/mrc.html REGISTRATION FEE Standard Registration: U.S. $750 ($950 after Jan 15, 1997) Student Registration: U.S. $450 ($530 after Jan 15, 1997) Student registrations - include copy of student ID. - Cancellation policy: No fee if cancellation before Jan 15, 1997. - Cancellation fee after January 15 but before Feb 12, 1997: $100. - Refund at discretion of organizers if cancellation after Feb 12, 1997. - Registration fee includes course materials, coffee breaks, and lunches - On-site Registration is possible if course is not fully booked, at late fee.Return to Top
Isn't this a path analysis question? The severity of the injury determines both the patients' health and the amount of time spent at the scence (with more severe injuries requiring a greater amount of time). In addition, the amount of time spent at the scene may have some effect on the patients' health. The researcher appear primarily interested in this path, especially whether the relationship is positive or negative. Severity of Injury | \ | \ | \ \/ \/ Time on Scene -------> Patient Health OutcomeReturn to Top
Here are some sources: BTW: Be careful with CHAID...it will usually find differences. Continue to test variables it finds by using a logistic regression model in the case of a categorical dependent variable and correlations and Anova for an interval or ratio level dependent variable. I usually split my sample into one or more parts too. One to develop the CHAID tree, and at least one other to test prediction accuracy on. Some early sources, though not probably what you are looking for. They suggest a general framework for classifcation analysis. W.A. Belson, "A technique for studying the effects of television broadcast", Applied Statistics, 5, 195 (1956). Lazarsfield, Paul, F. and Rosenberg, Morris (editors) The Lanugage of Social Research, A Reader in the Methodology of Social Research. Pg 118-120. Sonnquest, J.A. and Morgan, J.N. "The detection of interaction effects" (1964) Ann Arbor: Institute for Social Research, University of Michigan. - This resulted in the AID algorithm. Several papers by Leo Goodman. Starting with... Goodman, Leo, A. "On partioning chi squared and detecting partial association in three- way contingency tables." Journal of the Royal Statistical Society, Series B, 31. (1969) Goodman, Leo, A. ""The mulivariate analysis of qualitative data: interactions among multiple classifications." Journal of the American Statistical Association, 65, 226-56. - Reprinted in his book (1978) Analyzing Qualitative/Categorical Data, edited by J. Magidson, Cambridge, Massachusetts: Abt Books. Goodman, Leo, A. "The analysis of cross-classified data having ordered and/or unordered categories: association models, correlation models, and asymetry models for contingency tables with or without missing entries." The Annals of Statistics, 13(1), 10-69. (1985) - This was the start of Jay Magidson's enhancement to the CHAID model (see the last reference below) now implemented in SPSS's SI-CHAID and an option in SAS. I use KnowledgeSEEKER, but this enhancement has been made there. Goodman, Leo. A. "Measures, models and graphic displays in the analysis of cross-classified data." Journal of the American Statistical Association, 86, 1085-1138. (1991). Leo Brieman, J.H. Frieman, R.A. Olshen and C.J. Stone, Classification and Regression Trees (Wadsworth, 1984) Biggs, David, with Barry DeVille & Ed Suen. "A method of choosing multiway partitions for classification and decision trees" in the Journal of Applied Statistics, Vol 18, No. 1, )1991). - This is KnowledgeSEEKER's implementation of CHAID. G.V. Kass, "An exploratory technique for investigating large quantities of categorical data", Applied Statistics, 29, 2, 1980, 119-127. and really the same thing in D.M.Hawkins and G.V. Kass, "Automatic interaction detection", in D.G. Hawkins (ed.), Topics in Applied Multivariate Analysis (Cambridge, Cambridge University Press, 1982) - This was the basis for CHAID. Magidson, Jay, "Chi-squared analysis of a scalable dependent variable", Proceedings of the 1992 annual meeting of the American Statistical Association, Section on Statistical Education. (1992)Return to Top
In article <59ctcv$43g@news5.wavefront.com>, diffsimilar@wavefront.com says... I just read my own post. Jay Magidson's enhancement to the CHAID model, now implemented in SPSS's SI-CHAID has NOT been implemented in KnowledgeSEEKER. I typed the list too fast. Sorry 'bout that.Return to Top
The article you are looking for as a reference to CHAID can be found in the Journal of Marketing Research (JMR). I believe the year was 1978 and one of the two authors is Perreault. However, Perreault and his co-author reference a dissertation by Kass as the original reference. CHAID can also be purchased as a stand-along module from Statistical Innovations, Inc in Belmont, Mass. The principal of that company is Jay Magidson, who re-wrote Perreault's code and eventually licensed it to SPSS. He has written several articles in both JMR and the Journal of Direct Marketing on the use of CHAID, all very good reading. Steve Cohen Stratford Associates 617-928-0110 x104 StratfordA@aol.comReturn to Top
Hi there....would appreciate some assistance with the following: I am analyzing a data base with 153 in a treatment group and approximately 350 in the control group; the DV is cost of medical services with the procedure involving coronary bypass......the tx group may have only 3 or 4 patients with this procedure with possibly slightly more in the control group.....thus, the data points are predominantly 0 (zero).....obviously, any of the parametric statistics are inappropriate.....a colleague indicated that he recently purchased STATA which is able to analyze Poisson or Tobit distributions, which may suit my data....this is foreign territory for me......any suggestions how to compare the two groups when data points are primarily zero....the means make no sense (e.g., average of $200 for tx group).........is there anything in SPSS which is appropriate (e.g., using COMPUTE function to create Poisson distribution).. I am truly befuddled!!!....thank you and have a great holiday Dale Glaser Clinical Research; Sharp HealthCare dale.glaser@sharp.com daleglas@aol.comReturn to Top
In article <26222628@vixen.Dartmouth.EDU>, Haiyi XieReturn to Topwrites: |> We need to do regression analysis with RATIO (e.g., cost/benefit) as a |> dependent variable, but I was told that I might violate normal distribution |> assumption if I do so. Any comments, suggestions? Normality is not the main issue. When you compare two cost/benefit ratios, do you look at the difference of the ratios or the ratio of the ratios? I would guess the latter, in which case you should use the log of the cost/benefit ratio as the dependent variable. -- Warren S. Sarle SAS Institute Inc. The opinions expressed here saswss@unx.sas.com SAS Campus Drive are mine and not necessarily (919) 677-8000 Cary, NC 27513, USA those of SAS Institute. *** Do not send me unsolicited commercial or political email! ***
>Isn't this a path analysis question? The severity of the injury determines >both the patients' health and the amount of time spent at the scence (with >more severe injuries requiring a greater amount of time). In addition, the >amount of time spent at the scene may have some effect on the patients' >health. The researcher appear primarily interested in this path, especially >whether the relationship is positive or negative. > > Severity of Injury > | \ > | \ > | \ > \/ \/ > Time on Scene -------> Patient Health Outcome > Yes, but consider the problem of measurement error. Severity of injury is correlated with time on scene, but severity is measured with much more error than time. Thus, time will have a correlation with patient health outcome because it contains information on severity of injury that is not in the measures designed to measure severity. Imagine two cases where the severity of injury scores were the same but the crew spent more time on the scene in one case. This is likely to reflect unmeasured aspects of severity as well as variations in time on scene not due to severity. This will produce a spurious correlation. The more I think about it, the less I can imagine a model that would be an appropriate mapping of the process being studied onto a statistical procedure. _/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/ _/_/_/ _/_/ _/_/_/ _/ Ronan M Conroy _/ _/ _/ _/ _/ _/ Lecturer in Biostatistics _/_/_/ _/ _/_/_/ _/ Royal College of Surgeons _/ _/ _/ _/ _/ Dublin 2, Ireland _/ _/ _/_/ _/_/_/ _/ voice +353 1 402 2431 fax +353 1 402 2329 _/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/_/ 'Do not try to be a genius in every bar' [Brendan Behan? - No, Faure!]Return to Top