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From sequence to functional understanding: the difficult road ahead
DNA sequencing has become cheap, rapid and accurate, allowing us to access thousands of genomes and reveal the extensive variation among individuals. The major problem that arises from this is distinguishing between neutral and pathogenic variants. A recent study by Davis et al., in which a function...
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| Huvudupphovsmän: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BioMed Central
2011
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3129637/ https://ncbi.nlm.nih.gov/pubmed/21470392 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm235 |
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