Selected Talks

  • Molecular International Prognosis Scoring System for Myelodysplastic Syndromes ASH, December 2021.

  • Towards a Genetically-Inspired MDS Classification. ASH MDS Foundation Symposium, December 2021.

  • A clinical-molecular and personalized risk scoring system for patients with myelodysplastic syndromes. EMBL Cancer Genomics, November 2021.

  • TP53 in myeloid disease: implication of allelic state for genome stability and disease evolution. EHA, June 2021.

  • Population Genomics and Personalized Prognosis in Myelodysplastic Syndromes. European Bioconductor Meeting, December 2020.

  • TP53 State Dictates Genome Stability, Clinical Presentation and Outcomes in Myelodysplastic Syndromes. ASH, December 2019.

  • Mutational Impact on Diagnostic and Prognostic Evaluation of MDS. ASH MDS Foundation Symposium, December 2018.

  • A time- and cost-effective clinical diagnosis tool to quantify abnormal splicing from targeted single-gene RNA-seq. Splicing 2016, September 2016.

  • Deciphering splicing with sparse regression techniques in the era of high-throughput RNA sequencing. Journées MAS, Grande dimension et génomique, August 2016.

  • A convex formulation for joint RNA isoform detection and quantification from multiple RNA-seq samples. NIPS workshop on Computational Biology (MLCB), December 2014.

  • Fast isoform detection from RNA-Seq data with network flow techniques. ECCB'14 RADIANT Workshop, September 2014.

  • Kernel bilinear regression for toxicogenetics. RECOMB Conference on Regulatory and Systems Genomics, with DREAM Challenges, November 2013.

  • FlipFlop: Fast Lasso based Isoform Prediction as a FLOw Problem. HitSeq, July 2013.

  • Efficient sparse method for RNA isoforms identification and quantification from RNA-seq data with network flows. NIPS workshop on Computational Biology (MLCB), December 2012.