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In search of low-frequency and rare variants affecting complex traits

The allelic architecture of complex traits is likely to be underpinned by a combination of multiple common frequency and rare variants. Targeted genotyping arrays and next-generation sequencing technologies at the whole-genome sequencing (WGS) and whole-exome scales (WES) are increasingly employed t...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Panoutsopoulou, Kalliope, Tachmazidou, Ioanna, Zeggini, Eleftheria
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2013
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3782074/
https://ncbi.nlm.nih.gov/pubmed/23922232
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt376
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