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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...
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| Publicat a: | Nat Genet |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2014
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| Matèries: | |
| Accés en línia: | 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 |
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