Methods for copy number aberration detection from single-cell DNA-sequencing data
Abstract Copy number aberrations (CNAs), which are pathogenic copy number variations (CNVs), play an important role in the initiation and progression of cancer. Single-cell DNA-sequencing (scDNAseq) technologies produce data that is ideal for inferring CNAs. In this review, we review eight methods t...
| Published in: | Genome Biology |
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| Main Authors: | , , , |
| Format: | Article |
| Language: | English |
| Published: |
BMC
2020-08-01
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| Subjects: | |
| Online Access: | http://link.springer.com/article/10.1186/s13059-020-02119-8 |
