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Clinical utility of sequence-based genotype compared with that derivable from genotyping arrays
OBJECTIVE: We investigated the common-disease relevant information obtained from sequencing compared with that reported from genotyping arrays. MATERIALS AND METHODS: Using 187 publicly available individual human genomes, we constructed genomic disease risk summaries based on 55 common diseases with...
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| Päätekijät: | , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMJ Group
2012
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3392859/ https://ncbi.nlm.nih.gov/pubmed/22718036 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/amiajnl-2011-000737 |
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