Author

Amanda B Bradway

Broad Institute

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 1 Approach:experimental assay· 1 Organism:human· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Abebaw FekaduiD· 1 shared Adele PretoriusiD· 1 shared Alicia R. MartiniD· 1 shared Ana Maria OlivaresiD· 1 shared Anne StevensoniD· 1 shared Benjamin B. ChuiD· 1 shared Benjamin M. NealeiD· 1 shared Bizu GelayeiD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Abebaw FekaduORCID

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1 paper

Recent·Most cited

A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective manner

Toni A. Boltz, Benjamin B. Chu, Calwing Liao, Julia Sealock, Robert Ye, Lerato Majara, Jack M. Fu, Susan K. Service, Lingyu Zhan, Sarah Elizabeth Medland, Sinéad B. Chapman, Simone Rubinacci, Matthew T. DeFelice, Jonna Grimsby, Tamrat Abebe, , Alicia R. Martin

The paper introduces BGE, a sequencing method that combines low-pass whole genome and deep whole exome data, showing high accuracy and cost-effectiveness for genetic variant discovery.

bioRxiv · Sep 6, 2024 · PreprintGenomics