Loading...
Allele-specific copy-number discovery from whole-genome and whole-exome sequencing
Copy-number variants (CNVs) are a major form of genetic variation and a risk factor for various human diseases, so it is crucial to accurately detect and characterize them. It is conceivable that allele-specific reads from high-throughput sequencing data could be leveraged to both enhance CNV detect...
Saved in:
| Published in: | Nucleic Acids Res |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Oxford University Press
2015
|
| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4538801/ https://ncbi.nlm.nih.gov/pubmed/25883151 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkv319 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|