Eric Donaldson

The paper establishes reference samples with high-coverage whole-genome sequencing to create truth sets for somatic mutation and germline variant detection using NGS technologies.

This study evaluates reproducibility and accuracy of cancer mutation detection using whole-genome and whole-exome sequencing across multiple sequencing centers and bioinformatics pipelines.

The paper describes a crowdsourced challenge on precisionFDA to improve the BioCompute standard by gathering feedback and demonstrating BCO creation tools.