Author

Brian P. Landry

BillionToOne (United States)ORCID 0000-0001-6570-6950Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

David TsaoiD· 2 shared Oguzhan AtayiD· 2 shared Vivien SheehaniD· 2 shared Akila SubramaniamiD· 1 shared Amy B. NguyeniD· 1 shared Brian D. AlfordiD· 1 shared Celeste K. KanneiD· 1 shared Devon B. Chandler-BrowniD· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

David TsaoORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 2, 2021

Clinical validity of single-gene non-invasive prenatal testing for sickle cell disease and beta thalassemia

Erik R. Westin, David Tsao, Oguzhan Atay…·Vivien Sheehan

This study validates a single-gene non-invasive prenatal test (NIPT) for sickle cell disease and beta thalassemia, showing 100% concordance with newborn screening in 79 pregnancies.

2 citations

humanDNA methylation

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GeneticsScientific ReportsPeer-reviewedOct 7, 2019

A novel high-throughput molecular counting method with single base-pair resolution enables accurate single-gene NIPT

David Tsao, Sukrit Silas, Brian P. Landry…·Oguzhan Atay

This paper introduces a high-throughput molecular counting method with single base-pair resolution for accurate single-gene NIPT, achieving high sensitivity and specificity in detecting genetic disorders.

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humanwhole-genome sequencing

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