Author

Wayne Clarke

New York Genome Center

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

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Genomics· 1

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Approach:benchmark study· 1 Research Focus:benchmarking· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aaron M. WengeriD· 1 shared Álvaro Martínez BarrioiD· 1 shared Ana Stankovic· 1 shared Andrew W. CarrolliD· 1 shared Arend SidowiD· 1 shared Arkarachai FungtammasaniD· 1 shared Bohan NiiD· 1 shared Byunggil YooiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Aaron M. WengerORCID

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1 paper

Recent·Most cited

Benchmarking challenging small variants with linked and long reads

Justin Wagner, Nathan D. Olson, Lindsay N. Harris, Jennifer McDaniel, Ziad Khan, Jesse Farek, Medhat Mahmoud, Ana Stankovic, Vladimir Kovacevic, Byunggil Yoo, Neil Miller, Jeffrey Rosenfeld, Bohan Ni, Samantha Zarate, Melanie Kirsche, , Justin M. Zook

This paper expands genome benchmarking to include difficult-to-map regions using linked and long reads, identifying more false negatives in variant calling.

Cell Genomics · Apr 28, 2022Peer-reviewedGenomics