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American Journal of Human Genetics|November 3, 2023
Factorizing polygenic epistasis improves prediction and uncovers biological pathways in complex traitsDavid Tang, Jerome Freudenberg, Andy DahlGene|January 11, 2019
Alignment-free approaches for predicting novel Nuclear Mitochondrial Segments (NUMTs) in the human genomeWentian Li, Jerome Freudenberg, Jan FreudenbergAnnual Review of Genomics and Human Genetics|September 3, 2020
Genetic Influences on Disease SubtypesAndy Dahl, Noah ZaitlenBiorxiv : the Preprint Server for Biology|March 13, 2023
A robust model for cell type-specific interindividual variation in single-cell RNA sequencing dataMinhui Chen, Andy DahlNature Communications|June 19, 2024
A robust model for cell type-specific interindividual variation in single-cell RNA sequencing dataMinhui Chen, Andy DahlBiorxiv : the Preprint Server for Biology|May 18, 2026
Optimizing phenotype scale improves genetic analyses in large-scale biobanksZhenhong Huang, Manuela Costantino, Andy DahlGenetics|April 16, 2020
On Negative Heritability and Negative Estimates of HeritabilityDavid Steinsaltz, Andy Dahl, Kenneth W WachterAmerican Journal of Human Genetics|November 16, 2024
Allele frequency impacts the cross-ancestry portability of gene expression prediction in lymphoblastoid cell linesMarie Saitou, Andy Dahl, Qingbo Wang, et al.Genetics|January 30, 2019
Adjusting for Principal Components of Molecular Phenotypes Induces Replicating False PositivesAndy Dahl, Vincent Guillemot, Joel Mefford, et al.Genome Biology|January 28, 2026
Accurate variant effect estimation in FACS-based deep mutational scanning data with LilaceJerome Freudenberg, Jingyou Rao, Matthew K Howard, et al.Pageof 11