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Multiplexed assays of variant effects contribute to a growing genotype–phenotype atlas

Given the constantly improving cost and speed of genome sequencing, it is reasonable to expect that personal genomes will soon be known for many millions of humans. This stands in stark contrast with our limited ability to interpret the sequence variants which we find. Although it is, perhaps, easie...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Hum Genet
Asıl Yazarlar: Weile, Jochen, Roth, Frederick P.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Springer Berlin Heidelberg 2018
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6153521/
https://ncbi.nlm.nih.gov/pubmed/30073413
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-018-1916-x
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