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Sequencing Ultrarare Targets with Compound Nucleic Acid Cytometry

[Image: see text] Targeted sequencing enables sensitive and cost-effective analysis by focusing resources on molecules of interest. Existing methods, however, are limited in enrichment power and target capture length. Here, we present a novel method that uses compound nucleic acid cytometry to achie...

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Autores principales: Sun, Chen, Chang, Kai-Chun, Abate, Adam R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022902/
https://www.ncbi.nlm.nih.gov/pubmed/33971091
http://dx.doi.org/10.1021/acs.analchem.0c04749
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author Sun, Chen
Chang, Kai-Chun
Abate, Adam R.
author_facet Sun, Chen
Chang, Kai-Chun
Abate, Adam R.
author_sort Sun, Chen
collection PubMed
description [Image: see text] Targeted sequencing enables sensitive and cost-effective analysis by focusing resources on molecules of interest. Existing methods, however, are limited in enrichment power and target capture length. Here, we present a novel method that uses compound nucleic acid cytometry to achieve million-fold enrichments of molecules >10 kbp in length using minimal prior target information. We demonstrate the approach by sequencing HIV proviruses in infected individuals. Our method is useful for rare target sequencing in research and clinical applications, including for identifying cancer-associated mutations or sequencing viruses infecting cells.
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spelling pubmed-90229022022-04-25 Sequencing Ultrarare Targets with Compound Nucleic Acid Cytometry Sun, Chen Chang, Kai-Chun Abate, Adam R. Anal Chem [Image: see text] Targeted sequencing enables sensitive and cost-effective analysis by focusing resources on molecules of interest. Existing methods, however, are limited in enrichment power and target capture length. Here, we present a novel method that uses compound nucleic acid cytometry to achieve million-fold enrichments of molecules >10 kbp in length using minimal prior target information. We demonstrate the approach by sequencing HIV proviruses in infected individuals. Our method is useful for rare target sequencing in research and clinical applications, including for identifying cancer-associated mutations or sequencing viruses infecting cells. American Chemical Society 2021-05-10 2021-05-25 /pmc/articles/PMC9022902/ /pubmed/33971091 http://dx.doi.org/10.1021/acs.analchem.0c04749 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Sun, Chen
Chang, Kai-Chun
Abate, Adam R.
Sequencing Ultrarare Targets with Compound Nucleic Acid Cytometry
title Sequencing Ultrarare Targets with Compound Nucleic Acid Cytometry
title_full Sequencing Ultrarare Targets with Compound Nucleic Acid Cytometry
title_fullStr Sequencing Ultrarare Targets with Compound Nucleic Acid Cytometry
title_full_unstemmed Sequencing Ultrarare Targets with Compound Nucleic Acid Cytometry
title_short Sequencing Ultrarare Targets with Compound Nucleic Acid Cytometry
title_sort sequencing ultrarare targets with compound nucleic acid cytometry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022902/
https://www.ncbi.nlm.nih.gov/pubmed/33971091
http://dx.doi.org/10.1021/acs.analchem.0c04749
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