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Microfluidic droplet enrichment for targeted sequencing

Targeted sequence enrichment enables better identification of genetic variation by providing increased sequencing coverage for genomic regions of interest. Here, we report the development of a new target enrichment technology that is highly differentiated from other approaches currently in use. Our...

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Detalles Bibliográficos
Autores principales: Eastburn, Dennis J., Huang, Yong, Pellegrino, Maurizio, Sciambi, Adam, Ptáček, Louis J., Abate, Adam R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4513844/
https://www.ncbi.nlm.nih.gov/pubmed/25873629
http://dx.doi.org/10.1093/nar/gkv297
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author Eastburn, Dennis J.
Huang, Yong
Pellegrino, Maurizio
Sciambi, Adam
Ptáček, Louis J.
Abate, Adam R.
author_facet Eastburn, Dennis J.
Huang, Yong
Pellegrino, Maurizio
Sciambi, Adam
Ptáček, Louis J.
Abate, Adam R.
author_sort Eastburn, Dennis J.
collection PubMed
description Targeted sequence enrichment enables better identification of genetic variation by providing increased sequencing coverage for genomic regions of interest. Here, we report the development of a new target enrichment technology that is highly differentiated from other approaches currently in use. Our method, MESA (Microfluidic droplet Enrichment for Sequence Analysis), isolates genomic DNA fragments in microfluidic droplets and performs TaqMan PCR reactions to identify droplets containing a desired target sequence. The TaqMan positive droplets are subsequently recovered via dielectrophoretic sorting, and the TaqMan amplicons are removed enzymatically prior to sequencing. We demonstrated the utility of this approach by generating an average 31.6-fold sequence enrichment across 250 kb of targeted genomic DNA from five unique genomic loci. Significantly, this enrichment enabled a more comprehensive identification of genetic polymorphisms within the targeted loci. MESA requires low amounts of input DNA, minimal prior locus sequence information and enriches the target region without PCR bias or artifacts. These features make it well suited for the study of genetic variation in a number of research and diagnostic applications.
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spelling pubmed-45138442015-07-27 Microfluidic droplet enrichment for targeted sequencing Eastburn, Dennis J. Huang, Yong Pellegrino, Maurizio Sciambi, Adam Ptáček, Louis J. Abate, Adam R. Nucleic Acids Res Methods Online Targeted sequence enrichment enables better identification of genetic variation by providing increased sequencing coverage for genomic regions of interest. Here, we report the development of a new target enrichment technology that is highly differentiated from other approaches currently in use. Our method, MESA (Microfluidic droplet Enrichment for Sequence Analysis), isolates genomic DNA fragments in microfluidic droplets and performs TaqMan PCR reactions to identify droplets containing a desired target sequence. The TaqMan positive droplets are subsequently recovered via dielectrophoretic sorting, and the TaqMan amplicons are removed enzymatically prior to sequencing. We demonstrated the utility of this approach by generating an average 31.6-fold sequence enrichment across 250 kb of targeted genomic DNA from five unique genomic loci. Significantly, this enrichment enabled a more comprehensive identification of genetic polymorphisms within the targeted loci. MESA requires low amounts of input DNA, minimal prior locus sequence information and enriches the target region without PCR bias or artifacts. These features make it well suited for the study of genetic variation in a number of research and diagnostic applications. Oxford University Press 2015-07-27 2015-04-14 /pmc/articles/PMC4513844/ /pubmed/25873629 http://dx.doi.org/10.1093/nar/gkv297 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Eastburn, Dennis J.
Huang, Yong
Pellegrino, Maurizio
Sciambi, Adam
Ptáček, Louis J.
Abate, Adam R.
Microfluidic droplet enrichment for targeted sequencing
title Microfluidic droplet enrichment for targeted sequencing
title_full Microfluidic droplet enrichment for targeted sequencing
title_fullStr Microfluidic droplet enrichment for targeted sequencing
title_full_unstemmed Microfluidic droplet enrichment for targeted sequencing
title_short Microfluidic droplet enrichment for targeted sequencing
title_sort microfluidic droplet enrichment for targeted sequencing
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4513844/
https://www.ncbi.nlm.nih.gov/pubmed/25873629
http://dx.doi.org/10.1093/nar/gkv297
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