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Can whole-exome sequencing data be used for linkage analysis?
Whole-exome sequencing (WES) has become the strategy of choice to identify causal variants in monogenic disorders. However, the list of candidate variants can be quite large, including false positives generated by sequencing errors. To reduce this list of candidate variants to the most relevant ones...
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| Publicado no: | Eur J Hum Genet |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4929867/ https://ncbi.nlm.nih.gov/pubmed/26173971 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2015.143 |
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