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Microfluidics for genome-wide studies involving next generation sequencing

Next-generation sequencing (NGS) has revolutionized how molecular biology studies are conducted. Its decreasing cost and increasing throughput permit profiling of genomic, transcriptomic, and epigenomic features for a wide range of applications. Microfluidics has been proven to be highly complementa...

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Detalles Bibliográficos
Autores principales: Ma, Sai, Murphy, Travis W., Lu, Chang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AIP Publishing LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346105/
https://www.ncbi.nlm.nih.gov/pubmed/28396707
http://dx.doi.org/10.1063/1.4978426
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author Ma, Sai
Murphy, Travis W.
Lu, Chang
author_facet Ma, Sai
Murphy, Travis W.
Lu, Chang
author_sort Ma, Sai
collection PubMed
description Next-generation sequencing (NGS) has revolutionized how molecular biology studies are conducted. Its decreasing cost and increasing throughput permit profiling of genomic, transcriptomic, and epigenomic features for a wide range of applications. Microfluidics has been proven to be highly complementary to NGS technology with its unique capabilities for handling small volumes of samples and providing platforms for automation, integration, and multiplexing. In this article, we review recent progress on applying microfluidics to facilitate genome-wide studies. We emphasize on several technical aspects of NGS and how they benefit from coupling with microfluidic technology. We also summarize recent efforts on developing microfluidic technology for genomic, transcriptomic, and epigenomic studies, with emphasis on single cell analysis. We envision rapid growth in these directions, driven by the needs for testing scarce primary cell samples from patients in the context of precision medicine.
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spelling pubmed-53461052017-04-10 Microfluidics for genome-wide studies involving next generation sequencing Ma, Sai Murphy, Travis W. Lu, Chang Biomicrofluidics Review Articles Next-generation sequencing (NGS) has revolutionized how molecular biology studies are conducted. Its decreasing cost and increasing throughput permit profiling of genomic, transcriptomic, and epigenomic features for a wide range of applications. Microfluidics has been proven to be highly complementary to NGS technology with its unique capabilities for handling small volumes of samples and providing platforms for automation, integration, and multiplexing. In this article, we review recent progress on applying microfluidics to facilitate genome-wide studies. We emphasize on several technical aspects of NGS and how they benefit from coupling with microfluidic technology. We also summarize recent efforts on developing microfluidic technology for genomic, transcriptomic, and epigenomic studies, with emphasis on single cell analysis. We envision rapid growth in these directions, driven by the needs for testing scarce primary cell samples from patients in the context of precision medicine. AIP Publishing LLC 2017-03-10 /pmc/articles/PMC5346105/ /pubmed/28396707 http://dx.doi.org/10.1063/1.4978426 Text en © 2017 Author(s). 1932-1058/2017/11(2)/021501/24 All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review Articles
Ma, Sai
Murphy, Travis W.
Lu, Chang
Microfluidics for genome-wide studies involving next generation sequencing
title Microfluidics for genome-wide studies involving next generation sequencing
title_full Microfluidics for genome-wide studies involving next generation sequencing
title_fullStr Microfluidics for genome-wide studies involving next generation sequencing
title_full_unstemmed Microfluidics for genome-wide studies involving next generation sequencing
title_short Microfluidics for genome-wide studies involving next generation sequencing
title_sort microfluidics for genome-wide studies involving next generation sequencing
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346105/
https://www.ncbi.nlm.nih.gov/pubmed/28396707
http://dx.doi.org/10.1063/1.4978426
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