Author: Simon White

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Preprints

Genome-wide rare variant analysis for thousands of phenotypes in 54,000 exomes

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Selective constraints and pathogenicity of mitochondrial DNA variants inferred from a novel database of 196,554 unrelated individuals

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Quality Control and Integration of Genotypes from Two Calling Pipelines for Whole Genome Sequence Data in the Alzheimer's Disease Sequencing Project

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Atlas-CNV: a validated approach to call Single-Exon CNVs in the eMERGESeq gene panel

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Structures of three actinobacteriophage capsids: Roles of symmetry and accessory proteins

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