Microfluidics for genome-wide studies involving next generation sequencing

dc.contributor.authorMa, Saien
dc.contributor.authorMurphy, Travis W.en
dc.contributor.authorLu, Changen
dc.date.accessioned2020-11-09T16:06:25Zen
dc.date.available2020-11-09T16:06:25Zen
dc.date.issued2017-03-10en
dc.description.abstractNext-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.en
dc.description.sponsorshipWe acknowledge support from National Institutes of Health Grant Nos. CA174577, EB017235, EB019123, HG008623, and HG009256.en
dc.identifier.doihttps://doi.org/10.1063/1.4978426en
dc.identifier.urihttp://hdl.handle.net/10919/100808en
dc.identifier.volume11en
dc.language.isoen_USen
dc.publisherAIP Publishingen
dc.rightsCreative Commons Attribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.titleMicrofluidics for genome-wide studies involving next generation sequencingen
dc.title.serialBiomicrofluidicsen
dc.typeArticle - Refereeden

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