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Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy
BACKGROUND: We aimed to determine the mutation yield and clinical applicability of “molecular autopsy” following sudden arrhythmic death syndrome (SADS) by validating and utilizing low-cost high-throughput technologies: Fluidigm Access Array PCR-enrichment with Illumina HiSeq 2000 next generation se...
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| Publicat a: | BMC Cardiovasc Disord |
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| Autors principals: | , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6651896/ https://ncbi.nlm.nih.gov/pubmed/31337358 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12872-019-1154-8 |
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