Population Diversity at the Single-Cell Level

Author:

Gordon M. Grace1,Kathail Pooja2,Choy Bryson34,Kim Min Cheol34,Mazumder Thomas34,Gearing Melissa34,Ye Chun Jimmie5346

Affiliation:

1. 1Genentech, San Francisco, California, USA

2. 2Center for Computational Biology, University of California, Berkeley, California, USA

3. 3Division of Rheumatology, Department of Medicine, University of California, San Francisco, California, USA

4. 4Institute for Human Genetics, University of California, San Francisco, California, USA

5. 6Arc Institute, Palo Alto, California, USA

6. 5Bakar Computational Health Sciences Institute, Gladstone-UCSF Institute of Genomic Immunology, Parker Institute for Cancer Immunotherapy, Department of Epidemiology and Biostatistics, Department of Microbiology and Immunology, and Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, California, USA; email: jimmie.ye@ucsf.edu

Abstract

Population-scale single-cell genomics is a transformative approach for unraveling the intricate links between genetic and cellular variation. This approach is facilitated by cutting-edge experimental methodologies, including the development of high-throughput single-cell multiomics and advances in multiplexed environmental and genetic perturbations. Examining the effects of natural or synthetic genetic variants across cellular contexts provides insights into the mutual influence of genetics and the environment in shaping cellular heterogeneity. The development of computational methodologies further enables detailed quantitative analysis of molecular variation, offering an opportunity to examine the respective roles of stochastic, intercellular, and interindividual variation. Future opportunities lie in leveraging long-read sequencing, refining disease-relevant cellular models, and embracing predictive and generative machine learning models. These advancements hold the potential for a deeper understanding of the genetic architecture of human molecular traits, which in turn has important implications for understanding the genetic causes of human disease.

Publisher

Annual Reviews

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