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Parsing the Effects of Individual SNPs in Candidate Genes with Family Data
We introduce a stepwise approach for family-based designs for selecting a set of markers in a gene that are independently associated with the disease. The approach is based on testing the effect of a set of markers conditional on another set of markers. Several likelihood-based approaches have been...
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Päätekijät: | , , , , , , , |
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Aineistotyyppi: | Artigo |
Kieli: | Inglês |
Julkaistu: |
S. Karger AG
2010
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Aiheet: | |
Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2956011/ https://ncbi.nlm.nih.gov/pubmed/19996607 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000264447 |
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