We believe that basic research and the cultivation of scientific knowledge is critical for us to stay connected with our customers and to drive scientific breakthroughs. At NEB, over 30 labs participate in research projects, which are aided by post-doctoral fellows and students in Masters and Ph.D. programs. NEB researchers have authored or co-authored over 1,200 publications (as of 1/19) many of which are in peer-reviewed journals. Further, NEB products have been used successfully in numerous publications by scientists throughout the world.
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Your search returned 1993 results.
|2010||Open source tool for prediction of genome wide protein-protein interaction network based on ortholog information.||Source Code for Biology and Medicine||Pedamallu, C.and Posfai, J.|
|2019||Development of a high-throughput cytometric screen to identify anti-Wolbachia compounds: The power of public-private partnership||SLAS Discov||Clare, R.H., Clark, R., Bardelle, C., Harper, P., Collier, M., Johnston, K.L., Plant, H., Plant, D., McCall, E., Slatko, B.E., Cantin, L., Wu, B., Ford, L., Murray, D., Rich, K., Wigglesworth, M., Taylor, M.J., Ward, S.A.|
|2010||Gene synthesis of the bovine prochymosin gene and high-level expression in Kluyvermyces lactis||Sheng Wu Gong Cheng Xue Bao||Yuan W, et al.|
|2016||Epidemiological typing of Neisseria gonorrhoeae and detection of markers associated with antimicrobial resistance directly from urine samples using next generation sequencing||Sex. Transm. Infect||Graham, R.M.A. et al.|
|2013||Massively parallel characterization of restriction endonucleases||Scopus||Kamps-Hughes, N., Quimby, A., Zhu, Z., Johnson, E.A.|
|2002||Inteins in microbial genomes: distribution, mechanism and function.||Scientific World Journal 2||Southworth, M.W.and Perler, F.B.|
|2016||Advanced uracil DNA glycosylase-supplemented real-time reverse transcription loop-mediated isothermal amplification (UDG-rRT-LAMP) method for universal and specific detection of Tembusu virus||Scientific Reports||Tang Y, Chen H, Diao Y|
|2015||Restriction Cascade Exponential Amplification (RCEA) assay with an attomolar detection limit: a novel, highly specific, isothermal alternative to qPCR||Scientific Reports|
|2015||Expression and purification of single-chain Type IV restriction enzyme Eco94GmrSD and determination of it substrate preference||Scientific Reports||He, X., Hull, V., Thomas, J.A., Fu, X., Gidwani, S., Gupta, Y.K., Black, L.W. and Xu, S-Y.|
|2018||Targeted enrichment outperforms other enrichment techniques and enables more multi-species RNA-Seq analyses||Scientific Reports||Chung, M., Teigen, L., Liu, H., Libro, S., Shetty, A., Kumar, N., Zhao, X., Bromley, R. E., Tallon, L. J., Sadzewicz, L., Fraser, C. M., Rasko, D. A., Filler, S. G., Foster, J. M., Michalski, M. L., Bruno, V. M. and Dunning Hotopp, J. C.|