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 <rdf:Description>
  <dc:title>Design of experiments for detection of linkage disequilibrium</dc:title>
  <dc:subject>CRAN Task View: ExperimentalDesign (http://CRAN.R-project.org/view=ExperimentalDesign)</dc:subject>
  <dc:subject>CRAN Task View: Genetics (http://CRAN.R-project.org/view=Genetics)</dc:subject>
  <dc:description>R package for design of experiments for design of
genome-wide association studies.  Version 2 incorporating
quantitative traits and case-control studies. The Bayes factor
should be chosen large enough to give respectable posterior
odds. This requires Bayes factors of the order of 10^6 in
genome-wide association studies where prior odds are low.
Sample sizes needed to get this strength of evidence are
substantially higher than those from traditional power
calculations. The corresponding threshold for p-values is
substantially lower than commonly used.  For quantitative
traits ldDesign uses an existing deterministic power
calculation for detection of linkage disequilibrium between a
bi-allelic QTL and a bi-allelic marker, together with the
Spiegelhalter and Smith Bayes factor to generate designs with
power to detect effects with a given Bayes factor. For case-
control studies an asymptotic approximate Bayes factor is used
to derive an analytical power calculation in dominant,
recessive, additive and general genetic models.</dc:description>
  <dc:type>Software</dc:type>
  <dc:relation>Suggests: nlme (&gt;= 3.1.0)</dc:relation>
  <dc:creator>Rod Ball &lt;rod.ball@scionresearch.com&gt;</dc:creator>
  <dc:contributor>Rod Ball &lt;rod.ball@scionresearch.com&gt;</dc:contributor>
  <dc:rights>GPL (&gt;= 2)</dc:rights>
  <dc:date>2012-03-26</dc:date>
  <dc:format>application/tgz</dc:format>
  <dc:identifier>http://CRAN.R-project.org/package=ldDesign</dc:identifier>
 </rdf:Description>
</rdf:RDF>

