Wird geladen...
NPSV: A simulation-driven approach to genotyping structural variants in whole-genome sequencing data
BACKGROUND: Structural variants (SVs) play a causal role in numerous diseases but are difficult to detect and accurately genotype (determine zygosity) in whole-genome next-generation sequencing data. SV genotypers that assume that the aligned sequencing data uniformly reflect the underlying SV or us...
Gespeichert in:
| Veröffentlicht in: | Gigascience |
|---|---|
| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Oxford University Press
2021
|
| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8246072/ https://ncbi.nlm.nih.gov/pubmed/34195837 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/gigascience/giab046 |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|