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Rules for resolving Mendelian inconsistencies in nuclear pedigrees typed for two-allele markers
Gene-mapping studies, regularly, rely on examination for Mendelian transmission of marker alleles in a pedigree as a way of screening for genotyping errors and mutations. For analysis of family data sets, it is, usually, necessary to resolve or remove the genotyping errors prior to consideration. At...
Tallennettuna:
| Julkaisussa: | PLoS One |
|---|---|
| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Public Library of Science
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5333839/ https://ncbi.nlm.nih.gov/pubmed/28253278 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0172807 |
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