Wird geladen...
TAP: a targeted clinical genomics pipeline for detecting transcript variants using RNA-seq data
BACKGROUND: RNA-seq is a powerful and cost-effective technology for molecular diagnostics of cancer and other diseases, and it can reach its full potential when coupled with validated clinical-grade informatics tools. Despite recent advances in long-read sequencing, transcriptome assembly of short r...
Gespeichert in:
| Veröffentlicht in: | BMC Med Genomics |
|---|---|
| Hauptverfasser: | , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2018
|
| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6131862/ https://ncbi.nlm.nih.gov/pubmed/30200994 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-018-0402-6 |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|