Trouble Replicating Unstructured Mixed Procedure in R
Here's a typical agreement that users of SAS must agree to: Subject to the provisions contained herein, EMPLOYEE may use the SAS copyrighted computer software products which LICENSEE has provided in accordance with its agreement with SAS. EMPLOYEE acknowledges that these products are copyrighted and that SAS retains all title and ownership rights to the products. EMPLOYEE agrees not to copy or permit others to copy the products, in whole or in part. EMPLOYEE agrees to use the products under this agreement only on a computer which is owned or leased by LICENSEE and controlled by LICENSEE. EMPLOYEE further agrees that the products must remain under EMPLOYEE's control, and that resale or other transfer is explicitly prohibited. EMPLOYEE agrees to use the products only for EMPLOYEE's or LICENSEE's own data processing requirements, and not for commercial time-sharing, rental or service bureau use. EMPLOYEE agrees not to create, or attempt to create, or permit or help others to create, the source code from the products furnished under this agreement. EMPLOYEE agrees that it will not reverse engineer or decompile the products. (source: http://www.mcmaster.ca/uts/software_downloads/docs/SAS/saslicendform.doc ) Note that last paragraph. You can find it in other SAS end user license agreements. So anyone who tries to "replicate PROC MIXED for repeated measures set as unstructured in R" is then subject to legal action by the largest wealthiest statistical software company ever in existence. I personally am not up for that challenge, especially when the code has debateable merits. I'd rather write code from scratch using sound statistical first principles, which I can do thanks to the amazing amount of hard work by the R core group, none of whom have ever asked me to sign any agreement (though they do insist that I distribute source code and the GNU General Public License with any copies I modify and/or distribute). Steven McKinney Statistician Molecular Oncology and Breast Cancer Program British Columbia Cancer Research Centre From: Charles Determan Jr [mailto:deter088 at umn.edu] Sent: January-26-12 4:50 PM To: Steven McKinney Cc: r-sig-mixed-models at r-project.org Subject: Re: [R-sig-ME] Trouble Replicating Unstructured Mixed Procedure in R So am I to assume that this implies that there isn't any known way to replicate PROC MIXED for repeated measures set as unstructured in R? Charles
On Thu, Jan 26, 2012 at 6:36 PM, Steven McKinney <smckinney at bccrc.ca> wrote:
Since SAS does not publish its source code, replicating SAS code is not always possible (nor always desirable). R code is completely open, so can be studied, debated and replicated or modified - very useful when people want to engage in scientific discussions of statistical issues. Doing good science and data analysis is challenging when you are working with a black box of mysterious computer code. That's why statisticians have worked so hard for years to set up open source computational tools such as R. Steven McKinney Statistician Molecular Oncology and Breast Cancer Program British Columbia Cancer Research Centre
-----Original Message----- From: r-sig-mixed-models-bounces at r-project.org [mailto:r-sig-mixed-models- bounces at r-project.org] On Behalf Of Charles Determan Jr Sent: January-26-12 4:07 PM To: John Maindonald Cc: r-sig-mixed-models at r-project.org Subject: Re: [R-sig-ME] Trouble Replicating Unstructured Mixed Procedure in R The only thing I am looking for is the appropriate R code to replicate the SAS analysis shown in the previously mentioned paper. That is all I ask. What should the code be in order to analyze this 'dental' data to replicate the 'UN' or 'unstructured' analysis in the prior paper. Regards, Charles On Thu, Jan 26, 2012 at 4:37 PM, John Maindonald <john.maindonald at anu.edu.au
wrote:
It is not really a matter of computational accuracy. One can get highly accurate values for an inappropriate statistic. Or if there is insistence on using the word, accuracy, what is the meaning? i) the wrong formula is used? Then in what sense is it 'wrong'? ii) there is a numerical inaccuracy in the calculation? This is almost never an issue in a relatively simple calculation such as this, given the care taken by the code writers in such matters. iii) where an approximation is used, as in using an F-distribution approximation, is the best choice of degrees of freedom made to for use of this approximation? I judge that the degrees of freedom for lme's F-statistic for the interaction are not well chosen. Users really have to sort this out for themselves, rather than relying on what may be a fairly wild approximation that appears in lm's output. Using 75df rather than 25df does not however make the difference that a choice between (e.g.) 5df and 25df would. A further and more basic issue is whether the statistic that is provided is appropriate to the intended generalisation. I'd take this to be generalisation to another sample of youths from the same population. In order to understand why R and SAS are giving different F-statistics for the interaction, one needs to understand just what variance-covariance structure is assumed in each case. One might extract the two estimates of the var-cov structure and compare them. Look for terms in one that do not appear, or maybe that are zero, in the other. Finally, it is not just that Venables does not like type III SS. He is saying that they almost never correspond to a null hypothesis that makes any sense. Those who disagree try to write down the model to which the null hypothesis corresponds in testing for the main effect of factor1 with a factor1:factor2 interaction. John Maindonald email: john.maindonald at anu.edu.au phone : +61 2 (6125)3473 fax : +61 2(6125)5549 Centre for Mathematics & Its Applications, Room 1194, John Dedman Mathematical Sciences Building (Building 27) Australian National University, Canberra ACT 0200. http://www.maths.anu.edu.au/~johnm On 27/01/2012, at 2:41 AM, Thompson,Paul wrote:
OK, I've looked at that reference. There are 2 aspects of an estimate like a SS. The first is the
stability
of the estimate, and the second is the interpretation of the estimate.
The
issues with the interpretation of the different estimates go back to
1970,
and they are simply a matter of interpretation. The point of the Venables discussion is that he does not like Type III SS, not that they are wrong. He does not agree with the interpretation.
The issue here is the accuracy of the Type III or Type I or Type II or
whatever. Accuracy comes before interpretation. If the r module and SAS
do
not arrive at the same estimates, that is an important thing.
Once we agree upon computation, we can argue about interpretation.
Charles Determan is inquiring as to computational accuracy. The use and interpretation of the various Type I, II, III, IV, LVX SS are secondary.
-----Original Message----- From: r-sig-mixed-models-bounces at r-project.org [mailto:
r-sig-mixed-models-bounces at r-project.org] On Behalf Of Luca Borger
Sent: Thursday, January 26, 2012 9:03 AM To: r-sig-mixed-models at r-project.org Subject: Re: [R-sig-ME] Trouble Replicating Unstructured Mixed
Procedure
in R
I think: http://www.stats.ox.ac.uk/pub/MASS3/Exegeses.pdf HTH Luca Le 26/01/2012 15:52, Thompson,Paul a ?crit :
I am unfamiliar with this critique of Type III SS. Can you point me to
a reference discussing the difficulties with Type III SS?
-----Original Message----- From: r-sig-mixed-models-bounces at r-project.org [mailto:
r-sig-mixed-models-bounces at r-project.org] On Behalf Of John Maindonald
Sent: Wednesday, January 25, 2012 11:19 PM To: David Duffy Cc: r-sig-mixed-models at r-project.org Subject: Re: [R-sig-ME] Trouble Replicating Unstructured Mixed
Procedure in R
It is well to note that type III sums of squares are problematic. For testing the effects of a main effect, the null model is
constraining
the main effect in a manner that depends on the parameterisation. There are situations where it makes sense to fit interactions without main effects, and it is clear what constraint on the main effect is
the
relevant null (with an interaction between a factor and a variable, does one want all lines to go though the same point, or through perhaps the origin?), but that situation is unusual. For lines that are separate or all through the one point, one does not need type III sums of squares. Analyses often or frequently have enough genuine complications worrying (unless it is blindingly obvious that one ought to worry about it) without the rarely relevant complication of attending to a type III sum of squares. I'd guess that SAS and lme are, effectively, making different assumptions about the intended generalisation. They are clearly using different denominator degrees of freedom for F. As one is looking for consistency across the 27 different youths, SAS's denominator degrees of freedom for the interaction seem more or less right, pretty much equivalent to calculating slopes for females and slopes for males and using a t-test to compare them. (Sure, in the analyses presented, age has been treated as a categorical variable, but the comment still applies.) John Maindonald email: john.maindonald at anu.edu.au phone : +61 2 (6125)3473 fax : +61 2(6125)5549 Centre for Mathematics& Its Applications, Room 1194, John Dedman Mathematical Sciences Building (Building 27) Australian National University, Canberra ACT 0200. http://www.maths.anu.edu.au/~johnm On 26/01/2012, at 1:54 PM, David Duffy wrote:
On Tue, 24 Jan 2012, Charles Determan Jr wrote:
Greetings, I have been working on R for some time now and I have begun the
endeavor of
trying to replicate some SAS code in R. I have scoured the forums
but
This is also the Orthodont dataset, distributed with nlme. As David Atkins pointed out, R defaults to Type I SS. so you would
need to use, for example, the Anova() command from the car package. The other thing is that the SAS F statistics are only approximate, depending
on
which covariance structure is chosen (perhaps John Maindonald or someone clever could comment), so SAS offers different possibilities for ddf eg
http://www2.sas.com/proceedings/sugi26/p262-26.pdf while lme and lmer offer one or none. -- | David Duffy (MBBS PhD) ,-
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| email: davidD at qimr.edu.au ph: INT+61+7+3362-0217 fax: -0101 /
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| Epidemiology Unit, Queensland Institute of Medical Research \_,-
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| 300 Herston Rd, Brisbane, Queensland 4029, Australia GPG 4D0B994A
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