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  4. Negative Selection by Spiral Inertial Microfluidics Improves Viral Recovery and Sequencing from Blood

Negative Selection by Spiral Inertial Microfluidics Improves Viral Recovery and Sequencing from Blood

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sword-2019-06-05T14:59:51.original.xml (130 B)
Original SWORD entry document
Author(s)
Choi, Kyungyong
•
Ryu, Hyunryul
•
Siddle, Katherine J.
•
Piantadosi, Anne
•
Freimark, Lisa
•
Park, Daniel J.
•
Sabeti, Pardis
•
Han, Jongyoon
Date Issued
March 14, 2018
Journal
Analytical Chemistry
Publisher
American Chemical Society (ACS)
Citation
Choi, Kyungyong, et al. “Negative Selection by Spiral Inertial Microfluidics Improves Viral Recovery and Sequencing from Blood.” Analytical Chemistry 90, no. 7 (April 2018): 4657–62.
Version
Author's final manuscript
Abstract
In blood samples from patients with viral infection, it is often important to separate viral particles from human cells, for example, to minimize background in performing viral whole genome sequencing. Here, we present a microfluidic device that uses spiral inertial microfluidics with continuous circulation to separate host cells from viral particles and free nucleic acid. We demonstrate that this device effectively reduces white blood cells, red blood cells, and platelets from both whole blood and plasma samples with excellent recovery of viral nucleic acid. Furthermore, microfluidic separation leads to greater viral genome coverage and depth, highlighting an important application of this device in processing clinical samples for viral genome sequencing.
MIT Department
Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
Massachusetts Institute of Technology. Department of Biological Engineering
Massachusetts Institute of Technology. Research Laboratory of Electronics
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
https://hdl.handle.net/1721.1/121535
DOI of Published Version
https://doi.org/10.1021/acs.analchem.7b05200
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