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Naomi Sengamalay
Researcher at University of Maryland, Baltimore
Publications - 30
Citations - 4466
Naomi Sengamalay is an academic researcher from University of Maryland, Baltimore. The author has contributed to research in topics: Genome & Influenza A virus. The author has an hindex of 19, co-authored 30 publications receiving 3766 citations. Previous affiliations of Naomi Sengamalay include J. Craig Venter Institute.
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Journal ArticleDOI
An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform
Douglas Fadrosh,Bing Ma,Pawel Gajer,Naomi Sengamalay,Sandra Ott,Rebecca M. Brotman,Jacques Ravel +6 more
TL;DR: An improved dual-indexing amplification and sequencing approach to assess the composition of microbial communities from clinical samples using the V3-V4 region of the 16S rRNA gene on the Illumina MiSeq platform by introducing a 0 to 7 bp “heterogeneity spacer” to the index sequence that allows an equal proportion of samples to be sequenced out of phase.
Journal ArticleDOI
Direct detection of early-stage cancers using circulating tumor DNA
Jillian Phallen,Mark Sausen,Vilmos Adleff,Alessandro Leal,Carolyn Hruban,James R. White,Valsamo Anagnostou,Jacob Fiksel,Stephen Cristiano,Eniko Papp,Savannah Speir,Thomas Reinert,Mai-Britt Worm Ørntoft,Brian Woodward,Derek Murphy,Sonya Parpart-Li,David R. Riley,Monica Nesselbush,Naomi Sengamalay,Andrew Georgiadis,Qing Kay Li,Mogens Madsen,Frank Viborg Mortensen,Joost Huiskens,Cornelis J. A. Punt,Nicole C.T. van Grieken,Remond J.A. Fijneman,Gerrit A. Meijer,Hatim Husain,Robert B. Scharpf,Luis A. Diaz,Siân Jones,Samuel V. Angiuoli,Torben F. Ørntoft,Hans Jørgen Nielsen,Claus L. Andersen,Victor E. Velculescu +36 more
TL;DR: In patients with resectable colorectal cancers, higher amounts of preoperative circulating tumor DNA were associated with disease recurrence and decreased overall survival, and a method developed by Phallen et al., called targeted error correction sequencing, demonstrates the feasibility of detecting circulating cell-free DNA from many early tumors, suggesting its potential use for cancer screening.
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Large-scale sequencing of human influenza reveals the dynamic nature of viral genome evolution
Elodie Ghedin,Naomi Sengamalay,Martin Shumway,Jennifer Zaborsky,Tamara Feldblyum,Vik Subbu,David J. Spiro,Jeff Sitz,Hean Koo,Pavel Bolotov,Dmitry Dernovoy,Tatiana Tatusova,Yiming Bao,Kirsten St. George,Jill Taylor,David J. Lipman,Claire M. Fraser,Jeffery K. Taubenberger,Steven L. Salzberg,Steven L. Salzberg +19 more
TL;DR: A new, large-scale sequencing effort to provide a more comprehensive picture of the evolution of influenza viruses and of their pattern of transmission through human and animal populations is reported, encompassing a total of 2,821,103 nucleotides.
Journal ArticleDOI
The Evolutionary Genetics and Emergence of Avian Influenza Viruses in Wild Birds
Vivien G. Dugan,Rubing Chen,David J. Spiro,Naomi Sengamalay,Jennifer Zaborsky,Elodie Ghedin,Jacqueline M. Nolting,David E. Swayne,Jonathan A. Runstadler,George M. Happ,Dennis A. Senne,Ruixue Wang,Richard D. Slemons,Edward C. Holmes,Jeffery K. Taubenberger +14 more
TL;DR: It is proposed that AIV in wild birds forms transient “genome constellations,” continually reshuffled by reassortment, in contrast to the spread of a limited number of stable genome constellation that characterizes the evolution of mammalian-adapted influenza A viruses.
Journal ArticleDOI
Viral genome sequencing by random priming methods
Appolinaire Djikeng,Rebecca A. Halpin,Ryan Kuzmickas,Jay V. DePasse,Jeremy I. Feldblyum,Naomi Sengamalay,Claudio L. Afonso,Xinsheng Zhang,Norman G. Anderson,Elodie Ghedin,David J. Spiro +10 more
TL;DR: The SISPA methodology is adapted to genome sequencing of RNA and DNA viruses and of great utility in generating whole genome assemblies for viruses with little or no available sequence information, viruses from greatly divergent families, previously uncharacterized viruses, or to more fully describe mixed viral infections.