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Eugeni Namsaraev
Researcher at Stanford University
Publications - 17
Citations - 3689
Eugeni Namsaraev is an academic researcher from Stanford University. The author has contributed to research in topics: Internal medicine & Medicine. The author has an hindex of 10, co-authored 13 publications receiving 3371 citations. Previous affiliations of Eugeni Namsaraev include Life Technologies.
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Journal ArticleDOI
An integrated semiconductor device enabling non-optical genome sequencing
Jonathan M. Rothberg,Wolfgang Hinz,Todd Rearick,Jonathan Schultz,William J. Mileski,Melville Davey,John H. Leamon,Kim L. Johnson,Mark James Milgrew,Matthew D. Edwards,Jeremy Hoon,Jan Fredrik Simons,David Marran,Jason W. Myers,John F. Davidson,Annika Branting,John Nobile,Bernard P. Puc,David Light,Travis A. Clark,Martin Huber,Jeffrey T. Branciforte,Isaac B. Stoner,Simon Cawley,Michael R. Lyons,Yutao Fu,Nils Homer,Marina Sedova,Xin Miao,Brian Reed,Jeffrey Sabina,Erika Feierstein,Michelle Schorn,Mohammad Alanjary,Eileen T. Dimalanta,Devin Dressman,Rachel Kasinskas,Tanya Sokolsky,Jacqueline A. Fidanza,Eugeni Namsaraev,Kevin McKernan,Alan Williams,G. Thomas Roth,James Bustillo +43 more
TL;DR: A DNA sequencing technology in which scalable, low-cost semiconductor manufacturing techniques are used to make an integrated circuit able to directly perform non-optical DNA sequencing of genomes, showing its robustness and scalability by producing ion chips with up to 10 times as many sensors and sequencing a human genome.
Journal ArticleDOI
Multiplexed genotyping with sequence-tagged molecular inversion probes
Paul Hardenbol,Johan Baner,Maneesh Jain,Mats Nilsson,Eugeni Namsaraev,George Karlin-Neumann,Hossein Fakhrai-Rad,Mostafa Ronaghi,Thomas D. Willis,Ulf Landegren,Ronald W. Davis +10 more
TL;DR: The development of molecular inversion probe (MIP) genotyping is reported on, an efficient technology for large-scale single nucleotide polymorphism (SNP) analysis and multiplex analysis of more than 1,000 probes in a single tube can be done using standard laboratory equipment.
Journal ArticleDOI
Highly multiplexed molecular inversion probe genotyping: Over 10,000 targeted SNPs genotyped in a single tube assay
Paul Hardenbol,Fuli Yu,John W. Belmont,Jennifer MacKenzie,Carsten Bruckner,Tiffany Brundage,Andrew Boudreau,Steve Chow,Jim Eberle,Ayca Erbilgin,Mat Falkowski,Ron Fitzgerald,Sy Ghose,Oleg Iartchouk,Maneesh Jain,George Karlin-Neumann,Xiuhua Lu,Xin Miao,Bridget Moore,Martin Moorhead,Eugeni Namsaraev,Shiran Pasternak,Eunice Prakash,Karen Tran,Zhiyong Wang,Hywel B. Jones,Ronald W. Davis,Thomas D. Willis,Richard A. Gibbs +28 more
TL;DR: The suitability of Molecular Inversion Probe technology with four-color, single array detection, applied to large-scale genotyping of up to 12,000 SNPs per reaction is demonstrated, demonstrating the ability of the technology to suppress cross-reactivity at high multiplex levels.
Journal ArticleDOI
RNA profiles reveal signatures of future health and disease in pregnancy
Morten Rasmussen,Mitsu Reddy,Rory J. Nolan,Joan Camunas-Soler,Arkady B. Khodursky,Nikolai Madrid Scheller,David E. Cantonwine,Line Engelbrechtsen,Jia Dai Mi,Arup Dutta,Tiffany Brundage,Farooq Siddiqui,Mainou Thao,Elaine P.S. Gee,Johnny La,Courtney Baruch-Gravett,Mark K. Santillan,Saikat Deb,Shaali M. Ame,Said M. Ali,Melanie Adkins,Mark A. DePristo,Manfred Lee,Eugeni Namsaraev,D. Gybel-Brask,Lillian Skibsted,James A. Litch,Donna A. Santillan,Sunil Sazawal,Rachel M. Tribe,James M. Roberts,Maneesh Jain,Estrid Høgdall,Claudia Holzman,Stephen R. Quake,Michal A. Elovitz,Thomas F. McElrath +36 more
TL;DR: In this paper , the ability of plasma cell-free RNA (cfRNA) to reveal patterns of normal pregnancy progression and determine the risk of developing pre-eclampsia months before clinical presentation was demonstrated.
Journal ArticleDOI
Characterization of strand exchange activity of yeast Rad51 protein.
Eugeni Namsaraev,Paul Berg +1 more
TL;DR: The Saccharomyces cerevisiae RAD51 gene product takes part in genetic recombination and repair of DNA double strand breaks and catalyzes strand exchange between homologous circular single-stranded DNA (ssDNA) and linear double-stranding DNA (dsDNA) in the presence of ATP and ssDNA-binding protein.