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The human gene connectome as a map of short cuts for morbid allele discovery
High-throughput genomic data reveal thousands of gene variants per patient, and it is often difficult to determine which of these variants underlies disease in a given individual. However, at the population level, there may be some degree of phenotypic homogeneity, with alterations of specific physi...
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| Huvudupphovsmän: | , , , , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
National Academy of Sciences
2013
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3619280/ https://ncbi.nlm.nih.gov/pubmed/23509278 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1218167110 |
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