Development of a Fully Integrated “Sample-In-Answer-Out” System for Automatic Genetic Analysis: Springer Theses
Autor Bin Zhuangen Limba Engleză Hardback – 28 iul 2017
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Specificații
ISBN-13: 9789811047527
ISBN-10: 9811047529
Pagini: 114
Ilustrații: XXIII, 114 p. 58 illus., 44 illus. in color.
Dimensiuni: 155 x 235 mm
Greutate: 0.38 kg
Ediția:1st ed. 2018
Editura: Springer Nature Singapore
Colecția Springer
Seria Springer Theses
Locul publicării:Singapore, Singapore
ISBN-10: 9811047529
Pagini: 114
Ilustrații: XXIII, 114 p. 58 illus., 44 illus. in color.
Dimensiuni: 155 x 235 mm
Greutate: 0.38 kg
Ediția:1st ed. 2018
Editura: Springer Nature Singapore
Colecția Springer
Seria Springer Theses
Locul publicării:Singapore, Singapore
Cuprins
Introduction.- The construction of a general platform for capillary electrophoresis.- Integrated module for automatic DNA extraction and amplification.- A fully-integrated genetic analysis system.- Conclusion and prospects for future work.
Notă biografică
For internal review:
Dr. Bin Zhuang
Supervisor: Prof. Jing Cheng, School of Medicine, Tsinghua University
Current Affiliation: National Engineering Research Center for Beijing Biochip Technology, Capitalbio Corporation
Research Area: Biomedical engineering, microfluidic, nucleotide analysis, electrophoresis, biochemistry
Publications:
[1] Gan, W.P.,# Zhuang, B.,# Zhang, P.F., Han, J.P., Li, C.X., and Liu, P. (2014). A filter paper-based microdevice for low-cost, rapid, and automated DNA extraction and amplification from diverse sample types. Lab on a Chip 14, 3719-3728.
[2] Zhuang, B., # Gan, W.P., Wang, # S.Q., Han, J.P., Xiang, G.X., Li, C.X., Sun, J., Liu, P. (2015). A fully automated sample preparation microsystem for genetic testing of hereditary hearing loss using two-color multiplex allele-specific PCR. Analytical Chemistry, 87(2):1202-1209.
[3] Zhuang, B., # Han, J.P., # Xiang, G.X., Gan, W.P., Wang, S.Q., Wang, D., Wang, L., Sun, J., Li, C.X., Liu, P. (2016). A fully integrated and automated microsystem for rapid pharmacogenetic typing of multiple warfarin-related single-nucleotide polymorphisms. Lab on a Chip 16, 86-95.
Dr. Bin Zhuang
Supervisor: Prof. Jing Cheng, School of Medicine, Tsinghua University
Current Affiliation: National Engineering Research Center for Beijing Biochip Technology, Capitalbio Corporation
Research Area: Biomedical engineering, microfluidic, nucleotide analysis, electrophoresis, biochemistry
Publications:
[1] Gan, W.P.,# Zhuang, B.,# Zhang, P.F., Han, J.P., Li, C.X., and Liu, P. (2014). A filter paper-based microdevice for low-cost, rapid, and automated DNA extraction and amplification from diverse sample types. Lab on a Chip 14, 3719-3728.
[2] Zhuang, B., # Gan, W.P., Wang, # S.Q., Han, J.P., Xiang, G.X., Li, C.X., Sun, J., Liu, P. (2015). A fully automated sample preparation microsystem for genetic testing of hereditary hearing loss using two-color multiplex allele-specific PCR. Analytical Chemistry, 87(2):1202-1209.
[3] Zhuang, B., # Han, J.P., # Xiang, G.X., Gan, W.P., Wang, S.Q., Wang, D., Wang, L., Sun, J., Li, C.X., Liu, P. (2016). A fully integrated and automated microsystem for rapid pharmacogenetic typing of multiple warfarin-related single-nucleotide polymorphisms. Lab on a Chip 16, 86-95.
Textul de pe ultima copertă
This thesis reports on the development of a fully integrated and automated microsystem consisting of low-cost, disposable plastic chips for DNA extraction and PCR amplification, combined with a reusable glass capillary array electrophoresis chip, which can be employed in a modular-based format for genetic analysis. In the thesis, DNA extraction is performed by adopting a filter paper-based method, followed by an “in-situ” PCR carried out directly in the same reaction chamber of the chip without elution. PCR products are then co-injected with sizing standards into separation channels for detection using a novel injection electrode. The entire process is automatically carried out by a custom-made compact control and detection instrument. The author thoroughly tests the system’s performance and reliability by conducting rapid genetic screening of mutations on congenital hearing loss and pharmacogenetic typing of multiple warfarin-related single-nucleotide polymorphisms. The successful development and operation of this microsystem establishes the feasibility of rapid “sample-in-answer-out” testing in routine clinical practice.
Caracteristici
Nominated by Tsinghua University as an outstanding Ph.D. thesis Develops a disposable DNA extraction system and PCR microchip, as well as a compact control instrument for genetic testing of hereditary hearing loss from human whole blood with an improved turnaround time Describes a modular-based integration method for combining DNA extraction, PCR amplification, and capillary array electrophoresis in a single device Applies the integrated microsystem to the pharmacogenetic typing of multiple warfarin-related single-nucleotide polymorphisms