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Whole Genome Interpretation for a Family of Five

Although best practices have emerged on how to analyse and interpret personal genomes, the utility of whole genome screening remains underdeveloped. A large amount of information can be gathered from various types of analyses via whole genome sequencing including pathogenicity screening, genetic ris...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Front Genet
Päätekijät: Corpas, Manuel, Megy, Karyn, Mistry, Vanisha, Metastasio, Antonio, Lehmann, Edmund
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Frontiers Media S.A. 2021
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7982663/
https://ncbi.nlm.nih.gov/pubmed/33763108
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.535123
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