Microfluidics-free single-cell genomics with templated emulsification
QB3 · University of California, Berkeley · +8 more institutions
Abstract
Current single-cell RNA-sequencing approaches have limitations that stem from the microfluidic devices or fluid handling steps required for sample processing. We develop a method that does not require specialized microfluidic devices, expertise or hardware. Our approach is based on particle-templated emulsification, which allows single-cell encapsulation and barcoding of cDNA in uniform droplet emulsions with only a vortexer. Particle-templated instant partition sequencing (PIP-seq) accommodates a wide range of emulsification formats, including microwell plates and large-volume conical tubes, enabling thousands of samples or millions of cells to be processed in minutes. We demonstrate that PIP-seq produces…
Citation impact
- FWCI
- 30.86
- Percentile
- 100%
- References
- 82
Authors
25- ICIain C. ClarkCorresponding
QB3, University of California, Berkeley
- KMKristina M. Fontanez
Fluent (United States), Selecta Biosciences (United States)
- RHRobert H. Meltzer
Fluent (United States), Selecta Biosciences (United States)
- YXYi Xue
Fluent (United States), Selecta Biosciences (United States)
- CECorey E. Hayford
Fluent (United States), Selecta Biosciences (United States)
Topics & keywords
- Microfluidics
- Computational biology
- Single-cell analysis
- Workflow
- Nanotechnology
- Computer science
- Genomics
- DNA sequencing
Funding
- HHHoward Hughes Medical Institute
- ACAmerican Cancer SocietyAward: 132032-RSG-18-063-01-TBG
- DRDamon Runyon Cancer Research FoundationAward: CI-99-18
- LALeukemia and Lymphoma Society
- NINational Institutes of HealthAwards: K22AI152644, HG009490
- OOOffice of Extramural Research, National Institutes of HealthAwards: 1RM1HG009490-01, K99GM130964, K22AI152644, DP2AI154435, F31NS115380