Author

Benjamin L. Rambo‐Martin

Centers for Disease Control and PreventionORCID 0000-0002-8591-3954Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 2 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Assay:long-read sequencing· 1 Research Focus:sequence-to-function modeling· 1 Approach:statistical model· 1

Frequent Co-Authors

David E. WentworthiD· 3 shared John BarnesiD· 3 shared Malania M. WilsoniD· 3 shared Matthew W. KelleriD· 3 shared Justin S. LeeiD· 2 shared Kristine A. LacekiD· 2 shared Mili ShethiD· 2 shared Norman HasselliD· 2 shared

Activity by Year

2017-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenomics

David E. WentworthORCID

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4 papers

Recent·Most cited

GenomicsMicrobiology SpectrumPeer-reviewedDec 12, 2023

Targeted Amplification and Genetic Sequencing of the Severe Acute Respiratory Syndrome Coronavirus 2 Surface Glycoprotein

Matthew W. Keller, Lisa Mari Keong, Benjamin L. Rambo‐Martin…·John Barnes

The paper develops SpikeSeq, a targeted sequencing method for the SARS-CoV-2 S-gene, showing high conservation and accuracy across variants.

DOI 10.1128/spectrum.02982-23

whole-genome sequencingexperimental assay

GenomicsbioRxivPreprintMar 19, 2022

Identification of a Novel SARS-CoV-2 Delta-Omicron Recombinant Virus in the United States

Kristine A. Lacek, Benjamin L. Rambo‐Martin, Dhwani Govil Batra…·Clinton R. Paden

The paper identifies a novel SARS-CoV-2 Delta-Omicron recombinant virus in the United States with a hybrid Spike protein.

28 citations

humanexperimental assay

GenomicsScientific ReportsPeer-reviewedSep 20, 2018

Direct RNA Sequencing of the Complete Influenza A Virus Genome

Matthew W. Keller, Benjamin L. Rambo‐Martin, Malania M. Wilson…·John Barnes

The paper demonstrates direct RNA sequencing of the complete influenza A virus genome using a nanopore adapter, achieving 100% nucleotide coverage and high consensus identity.

144 citationstop 1%

viruslong-read sequencing

GenomicsG3 Genes Genomes GeneticsPeer-reviewedNov 15, 2017

Analysis of copy number variants on chromosome 21 in Down syndrome-associated congenital heart defects

Benjamin L. Rambo‐Martin, Jennifer Gladys Mulle, David J. Cutler…·Michael E. Zwick

This study investigates the association between copy number variants on chromosome 21 and congenital heart defects in Down syndrome, finding no direct link but suggesting ethnic differences in CNV patterns.

21 citations

humanwhole-genome sequencing