Comparison of genotype clustering tools with rare variants

BACKGROUND: Along with the improvement of high throughput sequencing technologies, the genetics community is showing marked interest for the rare variants/common diseases hypothesis. While sequencing can still be prohibitive for large studies, commercially available genotyping arrays targeting rare...

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Detalles Bibliográficos
Autores principales: Perreault, Louis-Philippe Lemieux, Legault, Marc-André, Barhdadi, Amina, Provost, Sylvie, Normand, Valérie, Tardif, Jean-Claude, Dubé, Marie-Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941951/
https://www.ncbi.nlm.nih.gov/pubmed/24559245
http://dx.doi.org/10.1186/1471-2105-15-52

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941951/
https://www.ncbi.nlm.nih.gov/pubmed/24559245
http://dx.doi.org/10.1186/1471-2105-15-52

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