Author

Sarah C. Reed

Broad InstituteORCID 0000-0003-2191-6643Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:variant effect prediction· 2 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Organism:human· 1 Research Focus:perturbation response prediction· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Atish Dipankar ChoudhuryiD· 2 shared Daniel G. StoveriD· 2 shared Gregory Gydush· 2 shared Heather Anne ParsonsiD· 2 shared Justin RhoadesiD· 2 shared Viktor A. AdalsteinssoniD· 2 shared Christopher Lo· 1 shared David KatziD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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2 shared papersBioinformatics

Atish Dipankar ChoudhuryORCID

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2 papers

Recent·Most cited

BioinformaticsNature CommunicationsPeer-reviewedMar 30, 2024

FinaleMe: Predicting DNA methylation by the fragmentation patterns of plasma cell-free DNA

Yaping Liu, Sarah C. Reed, Christopher Lo…·M Kellis

FinaleMe predicts DNA methylation and tissues-of-origin from plasma whole-genome sequencing by using a non-homogeneous Hidden Markov Model.

29 citationstop 3%

humanwhole-genome sequencing

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Molecular BiologybioRxivPreprintJan 22, 2021

MAESTRO affords 'breadth and depth' for mutation testing

Gregory Gydush, Erica Nguyen, Jin H. Bae…·Viktor A. Adalsteinsson

MAESTRO enables efficient and accurate tracking of thousands of low-frequency mutations with reduced sequencing, improving mutation testing in cancer and liquid biopsies.

5 citations

whole-exome sequencingexperimental assay

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