Thoas Fioretos
Research team manager
Single-cell sequencing in translational cancer research and challenges to meet clinical diagnostic needs
Author
Summary, in English
The ability to capture alterations in the genome or transcriptome by next-generation sequencing has provided critical insight into molecular changes and programs underlying cancer biology. With the rapid technological development in single-cell sequencing, it has become possible to study individual cells at the transcriptional, genetic, epigenetic, and protein level. Using single-cell analysis, an increased resolution of fundamental processes underlying cancer development is obtained, providing comprehensive insights otherwise lost by sequencing of entire (bulk) samples, in which molecular signatures of individual cells are averaged across the entire cell population. Here, we provide a concise overview on the application of single-cell analysis of different modalities within cancer research by highlighting key articles of their respective fields. We furthermore examine the potential of existing technologies to meet clinical diagnostic needs and discuss current challenges associated with this translation.
Department/s
- Center for Translational Genomics (CTG)
- LUCC: Lund University Cancer Centre
- Translational Genomic and Functional Studies of Leukemia
- Division of Clinical Genetics
- Stem Cells and Leukemia
- Division of Molecular Hematology (DMH)
- StemTherapy: National Initiative on Stem Cells for Regenerative Therapy
- Department of Laboratory Medicine
Publishing year
2021-07-01
Language
English
Pages
504-524
Publication/Series
Genes, Chromosomes and Cancer
Volume
60
Issue
7
Document type
Journal article review
Publisher
John Wiley & Sons Inc.
Topic
- Cancer and Oncology
Status
Published
Research group
- Translational Genomic and Functional Studies of Leukemia
- Stem Cells and Leukemia
ISBN/ISSN/Other
- ISSN: 1045-2257