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Decoding the antibody repertoire = h...
~
DeKosky, Brandon.
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Decoding the antibody repertoire = high throughput sequencing of multiple transcripts from single b cells /
Record Type:
Electronic resources : Monograph/item
Title/Author:
Decoding the antibody repertoire/ by Brandon DeKosky.
Reminder of title:
high throughput sequencing of multiple transcripts from single b cells /
Author:
DeKosky, Brandon.
Published:
Cham :Springer International Publishing : : 2017.,
Description:
xxviii, 87 p. :ill., digital ;24 cm.
[NT 15003449]:
Background -- High-throughput Sequencing of the Paired Human Immunoglobulin Heavy and Light Chain Repertoire -- In-Depth Determination and Analysis of the Human Paired Heavy and Light Chain Antibody Repertoire -- Paired VH:VL Analysis of Naive B Cell Repertoires and Comparison to Antigen-Experienced B Cell Repertoires in Healthy Human Donors -- Conclusions and Future Perspectives -- Appendices.
Contained By:
Springer eBooks
Subject:
B cells - Research. -
Online resource:
http://dx.doi.org/10.1007/978-3-319-58518-5
ISBN:
9783319585185
Decoding the antibody repertoire = high throughput sequencing of multiple transcripts from single b cells /
DeKosky, Brandon.
Decoding the antibody repertoire
high throughput sequencing of multiple transcripts from single b cells /[electronic resource] :by Brandon DeKosky. - Cham :Springer International Publishing :2017. - xxviii, 87 p. :ill., digital ;24 cm. - Springer theses,2190-5053. - Springer theses..
Background -- High-throughput Sequencing of the Paired Human Immunoglobulin Heavy and Light Chain Repertoire -- In-Depth Determination and Analysis of the Human Paired Heavy and Light Chain Antibody Repertoire -- Paired VH:VL Analysis of Naive B Cell Repertoires and Comparison to Antigen-Experienced B Cell Repertoires in Healthy Human Donors -- Conclusions and Future Perspectives -- Appendices.
This thesis outlines the development of the very first technology for high-throughput analysis of paired heavy and light-chain antibody sequences, opening the door for the discovery of new antibodies and the investigation of adaptive immune responses to vaccines and diseases. By designing two new technologies for sequencing multiple mRNA transcripts from up to 10 million isolated, single cells, the author directly addresses the limitations to provide information on the identity of immune receptor pairs encoded by individual B or T lymphocytes. Previous methods for high-throughput immune repertoire sequencing have been unable to provide such information. The techniques developed in this thesis have enabled comprehensive investigation of human B-cell repertoires and have been applied for the rapid discovery of new human antibodies, to gain new insights into the development of human antibody repertoires, and for analysis of human immune responses to vaccination and disease.
ISBN: 9783319585185
Standard No.: 10.1007/978-3-319-58518-5doiSubjects--Topical Terms:
3241637
B cells
--Research.
LC Class. No.: QR185.8.B15
Dewey Class. No.: 616.0798
Decoding the antibody repertoire = high throughput sequencing of multiple transcripts from single b cells /
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Background -- High-throughput Sequencing of the Paired Human Immunoglobulin Heavy and Light Chain Repertoire -- In-Depth Determination and Analysis of the Human Paired Heavy and Light Chain Antibody Repertoire -- Paired VH:VL Analysis of Naive B Cell Repertoires and Comparison to Antigen-Experienced B Cell Repertoires in Healthy Human Donors -- Conclusions and Future Perspectives -- Appendices.
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This thesis outlines the development of the very first technology for high-throughput analysis of paired heavy and light-chain antibody sequences, opening the door for the discovery of new antibodies and the investigation of adaptive immune responses to vaccines and diseases. By designing two new technologies for sequencing multiple mRNA transcripts from up to 10 million isolated, single cells, the author directly addresses the limitations to provide information on the identity of immune receptor pairs encoded by individual B or T lymphocytes. Previous methods for high-throughput immune repertoire sequencing have been unable to provide such information. The techniques developed in this thesis have enabled comprehensive investigation of human B-cell repertoires and have been applied for the rapid discovery of new human antibodies, to gain new insights into the development of human antibody repertoires, and for analysis of human immune responses to vaccination and disease.
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Biomedical and Life Sciences (Springer-11642)
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W9321223
電子資源
11.線上閱覽_V
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EB QR185.8.B15
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