Massively multiplex chemical transcriptomics at single-cell resolution

Author:

Srivatsan Sanjay R.12ORCID,McFaline-Figueroa José L.1ORCID,Ramani Vijay13ORCID,Saunders Lauren1ORCID,Cao Junyue1ORCID,Packer Jonathan1ORCID,Pliner Hannah A.1ORCID,Jackson Dana L.1ORCID,Daza Riza M.1ORCID,Christiansen Lena4ORCID,Zhang Fan4ORCID,Steemers Frank4,Shendure Jay1567ORCID,Trapnell Cole157ORCID

Affiliation:

1. Department of Genome Sciences, University of Washington, Seattle, WA, USA.

2. Medical Scientist Training Program, University of Washington, Seattle, WA, USA.

3. Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA, USA.

4. Illumina Inc., San Diego, CA, USA.

5. Allen Discovery Center for Cell Lineage Tracing, Seattle, WA, USA.

6. Howard Hughes Medical Institute, University of Washington, Seattle, WA, USA.

7. Brotman Baty Institute for Precision Medicine, Seattle, WA, USA.

Abstract

Single-cell chemical transcriptomics Single-cell transcriptomic technologies have emerged as powerful tools to explore cellular heterogeneity at the resolution of individual cells. Srivatsan et al. now add another layer of information and complexity by combining single-cell transcriptomics with oligo hashing and small molecule screening in a method called sci-Plex. Because screening many chemical compounds requires the ability to profile many cells, and because screens perturb cells in many different ways, the authors demonstrate the effects of 188 compounds in three cancer lines. The sci-Plex method can capture gene expression profiles from thousands of experimental conditions in a single experiment. Science , this issue p. 45

Funder

National Science Foundation

Howard Hughes Medical Institute

National Human Genome Research Institute

W.M. Keck Foundation

Paul G. Allen Frontiers Group

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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