Single-Cell Genomics

Author:

Paolillo Carmela1,Londin Eric2,Fortina Paolo34

Affiliation:

1. Division of Precision and Computational Diagnostics, Department of Clinical Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA

2. Computational Medicine Center, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA

3. Department of Cancer Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA

4. Department of Molecular Medicine, Sapienza University, Rome, Italy

Abstract

AbstractBACKGROUNDSingle-cell genomics is an approach to investigate cell heterogeneity and to identify new molecular features correlated with clinical outcomes. This approach allows identification of the complexity of cell diversity in a sample without the loss of information that occurs when multicellular or bulk tissue samples are analyzed.CONTENTThe first single-cell RNA-sequencing study was published in 2009, and since then many more studies and single-cell sequencing methods have been published. These studies have had a major impact on several fields, including microbiology, neurobiology, cancer, and developmental biology. Recently, improvements in reliability and the development of commercial single-cell isolation platforms are opening the potential of this technology to the clinical laboratory.SUMMARYIn this review we provide an overview of the current state of single-cell genomics. We describe opportunities in clinical research and medical applications.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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