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Examining the Impact of Imputation Errors on Fine-Mapping Using DNA Methylation QTL as a Model Trait
Genetic variants disrupting DNA methylation at CpG dinucleotides (CpG-SNP) provide a set of known causal variants to serve as models to test fine-mapping methodology. We use 1716 CpG-SNPs to test three fine-mapping approaches (Bayesian imputation-based association mapping, Bayesian sparse linear mix...
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| Vydáno v: | Genetics |
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| Hlavní autoři: | , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Genetics Society of America
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6614908/ https://ncbi.nlm.nih.gov/pubmed/31040117 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.118.301861 |
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