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Prioritization of family member sequencing for the detection of rare variants
BACKGROUND: The advent of affordable sequencing has enabled researchers to discover many variants contributing to disease, including rare variants. There are methods for determining the most informative individuals for sequencing, but the application of these methods is more complex when working wit...
Tallennettuna:
| Julkaisussa: | BMC Proc |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5133500/ https://ncbi.nlm.nih.gov/pubmed/27980641 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12919-016-0035-8 |
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