Peter D. Stenson

AVADA Enables Automated Genetic Variant Curation Directly from the Full Text Literature

David Neil Cooper, Maximilian Haeussler, Gill Bejerano, 2018, bioRxiv.

A Probabilistic Model to Predict Clinical Phenotypic Traits from Genome Sequencing

Cheng Wang, Biao Li, Sean D. Mooney, 2014, PLoS Comput. Biol..

CRAVAT: cancer-related analysis of variants toolkit

Hannah Carter, Mark Diekhans, Peter D. Stenson, 2013, Bioinform..

AMELIE accelerates Mendelian patient diagnosis directly from the primary literature

Gill Bejerano, Johannes Birgmeier, Peter D. Stenson, 2017, bioRxiv.

Blacklisting variants common in private cohorts but not in public databases optimizes human exome analysis

Jacques Fellay, Peter D. Stenson, David N. Cooper, 2018, Proceedings of the National Academy of Sciences.

MuPIT interactive: webserver for mapping variant positions to annotated, interactive 3D structures

Mark Diekhans, Peter D. Stenson, Rachel Karchin, 2013, Human Genetics.

Consortium, G.P A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073

Ken Chen, Joshua M. Korn, Afidalina Tumian, 2010 .

A Massively Parallel Pipeline to Clone DNA Variants and Examine Molecular Phenotypes of Human Disease Mutations

Matthew Mort, Peter D. Stenson, Xiaomu Wei, 2014, PLoS genetics.