Recent work (noted since 2001; numbers from CV) has been largely in statistical genomics, concerning data analysis, methodology and design [A 50--52, 54--65, 67, 76--78; B 2--3, 4; E 9--11]. Methodology research on quantitative trait loci (QTL) has addressed linkage map construction [A 54--55], semi-parametric and non-parametric inference [A 52, 57, 61, 63, 73; E 10], experimental design [A 64], Bayesian model selection [A 67, 79--81], and expression QTL or genetical genomics [A 60, 68, 70--71, 82, 84--85], and fine mapping [A 68, 72]. Several additional applied collaborations have involved microarray analysis [A 56, 58--59, 62, 65, 69, 75; B 1; E 9]. Bayesian model selection for genetic architecture (location and gene action of multiple QTL) has been a major thrust of methodological research, largely in the development of computational resources. I have subcontracts on two NIH software development grants, with Karl Broman, Johns Hopkins U, and Gary Churchill, Jackson Laboratory, and with Nengjun Yi and David Allison at U AL Birmingham. These involve enhancements to the widely used R/qtl library and a new Bayesian model selection library (R/qtlbim) was released in 2006 [A 78]; a QTL-dependent phenotype causal graph package (R/qdg) was released in Summer 2008.
Files in these folders include published and unpublished work of Brian S. Yandell. See my Curriculum Vitae or Publications for the full list with hot links. Numbers before journal name indicates CV order; letters before numbers indicate section in CV. Copies of published papers provided under fair use guidelines (see for instance http://fairuse.stanford.edu). About 10% of papers are not yet available in electronic form.
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For those interested in Paul Erdös, my Erdös number is 3. I have coauthored with Lajos Horváth, Miklós Csörgő and Dave M Mason. Lajos and Miklós both coauthored papers with Pál Révész among others, who in turn coauthored several papers with Paul Erdös. See the Erdös Number Project. Thus any coauthor of mine has an Erdös number at most 4.
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