Scalable microfluidics for single-cell RNA printing and sequencing

111Citations
Citations of this article
277Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Many important biological questions demand single-cell transcriptomics on a large scale. Hence, new tools are urgently needed for efficient, inexpensive manipulation of RNA from individual cells. We report a simple platform for trapping single-cell lysates in sealed, picoliter microwells capable of printing RNA on glass or capturing RNA on beads. We then develop a scalable technology for genome-wide, single-cell RNA-Seq. Our device generates pooled libraries from hundreds of individual cells with consumable costs of $0.10-$0.20 per cell and includes five lanes for simultaneous experiments. We anticipate that this system will serve as a general platform for single-cell imaging and sequencing.

Cite

CITATION STYLE

APA

Bose, S., Wan, Z., Carr, A., Rizvi, A. H., Vieira, G., Pe’er, D., & Sims, P. A. (2015). Scalable microfluidics for single-cell RNA printing and sequencing. Genome Biology, 16(1). https://doi.org/10.1186/s13059-015-0684-3

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free