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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer Berlin Heidelberg
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6153521/ https://www.ncbi.nlm.nih.gov/pubmed/30073413 http://dx.doi.org/10.1007/s00439-018-1916-x |