|
|
Selected ContributionsSelected Presentations (book of abstracts)A fast homotopy algorithm for a large class of weighted classification problems and application to phylogeny (pdf) Multi-trait genomic selection via multivariate regression with structured regularization (pdf) Identifying Differentially Expressed Proteins by a Binary Threshold Model (pdf) Testing for Associations between Loci and Environmental Gradients Using Latent Factor Mixed Models (pdf) Evolution of Codon Usage Bias in E. coli (pdf) A New Gene-Based test of Association Using Extended Rasch Models (pdf) A Regularisation Path-Following Approach for Discovering Interactions in High-Dimensional Survival Data (pdf) The Causal Mediation Analysis in Genomic Data (pdf) On the robustness of the Generalized Fused Lasso to prior specifications (pdf) Testing 2 x 2 Association with Uncertain Classification (pdf) An RNA-Seq read count emission model for transcriptional landscape reconstruction with state-space models (pdf) The leave-p-out estimator of the prediction error as a U-statistic and its asymptotic tests (pdf) Of cis, trans, and feedback regulation: Dissecting local regulation in yeast (pdf) Efficient statistical computations on genome-scale data using reduced representations (pdf) Selected PostersP1. Statistical Integration of Genotypic and Phenotypic Data Towards Starter Prediction P2. Cytopathic Effects Influence the Phenotype P3. An exact method to calculate the expected allelic diversity P4. Tracts of identity: length distribution, evolutionary history and applications P5. The impact of agricultural emergence on the genomes of African rainforest hunter-gatherers and agriculturalists P6. Statistical properties of the site-frequency spectrum associated with Lambda-coalescents P7. Synteny Units in Bacteria: A Universal Law Shaped by Selection P8. Modeling the evolution of gene relationships P9. Meta-analysis of incomplete Microarray Studies P10. Causal inference of gene expression in a neoadjuvant phase II trial of breast cancer P11. Polygene Scoring to investigate shared risk genes in disorders comorbid with Major Depressive Disorder P12. Calling genotypes in pooled samples and polyploid genomes P13. Analysis of genomic markers: make it easy with the R package MPAgenomics |