Author

Amelia D. Wallace

University of UtahORCID 0000-0001-9812-4236Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Approach:experimental assay· 1 Assay:long-read sequencing· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aaron R. QuinlaniD· 2 shared Brent S. PederseniD· 2 shared Brooke L. GatesiD· 1 shared D. Hunter BestiD· 1 shared Harriet DashnowiD· 1 shared Jeff Greenland· 1 shared Joe BrowniD· 1 shared Jordan Swanier· 1 shared

Activity by Year

2021-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersBioinformatics

Aaron R. QuinlanORCID

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2 papers

Recent·Most cited

Bioinformaticsnpj Genomic MedicinePeer-reviewedJul 15, 2021

Effective variant filtering and expected candidate variant yield in studies of rare human disease

Brent S. Pedersen, Joe Brown, Harriet Dashnow…·Aaron R. Quinlan

The paper establishes variant filtering guidelines for rare disease studies and estimates candidate variant yields for different inheritance modes using slivar software.

122 citationstop 1%

humanwhole-genome sequencing

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GeneticsPLoS ONEPeer-reviewedApr 8, 2021

CaBagE: a Cas9-based Background Elimination strategy for targeted, long-read DNA sequencing

Amelia D. Wallace, Thomas A. Sasani, Jordan Swanier…·Aaron R. Quinlan

CaBagE is a method for enriching target DNA regions for long-read sequencing, achieving high coverage and enabling analysis of complex genomic loci in disease contexts.

29 citations

humanlong-read sequencing

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