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Simulating pedigrees ascertained for multiple disease-affected relatives
BACKGROUND: Studies that ascertain families containing multiple relatives affected by disease can be useful for identification of causal, rare variants from next-generation sequencing data. RESULTS: We present the R package SimRVPedigree, which allows researchers to simulate pedigrees ascertained on...
Tallennettuna:
| Julkaisussa: | Source Code Biol Med |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6190569/ https://ncbi.nlm.nih.gov/pubmed/30356812 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13029-018-0069-6 |
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