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List of works by Aaron M Wenger

A crowdsourced set of curated structural variants for the human genome

scientific article published on 19 June 2020

A robust benchmark for detection of germline large deletions and insertions

scientific article published on 15 June 2020

AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literature

scientific article published on 01 May 2020

Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome

scientific article published on 12 August 2019

An MTF1 binding site disrupted by a homozygous variant in the promoter of ATP7B likely causes Wilson Disease

scientific article published on 07 August 2018

Author Correction: A robust benchmark for detection of germline large deletions and insertions

scientific article published on 22 July 2020

High-coverage, long-read sequencing of Han Chinese trio reference samples.

scientific article

Multi-platform discovery of haplotype-resolved structural variation in human genomes

scientific article published on 16 April 2019

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