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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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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. |
format | Online Article Text |
id | pubmed-4513844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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