Nalaganje...
Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications
High-throughput DNA sequencing technology has transformed genetic research and is starting to make an impact on clinical practice. However, analyzing high-throughput sequencing data remains challenging, particularly in clinical settings where accuracy and turnaround times are critical. We present a...
Shranjeno v:
| izdano v: | Nat Genet |
|---|---|
| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2014
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4753679/ https://ncbi.nlm.nih.gov/pubmed/25017105 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.3036 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|