Personalized genomic disease risk of volunteers
Next-generation sequencing (NGS) is commonly used for researching the causes of genetic disorders. However, its usefulness in clinical practice for medical diagnosis is in early development. In this report, we demonstrate the value of NGS for genetic risk assessment and evaluate the limitations and...
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| Main Authors: | , , , |
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| Format: | Text |
| Language: | English |
| Published: |
National Academy of Sciences
2013
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| Subjects: | |
| Online Access: | https://pmc.ncbi.nlm.nih.gov/articles/PMC3801013/ https://pubmed.ncbi.nlm.nih.gov/24082139 http://dx.doi.org/10.1073/pnas.1315934110 |
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