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VarMod: modelling the functional effects of non-synonymous variants
Unravelling the genotype–phenotype relationship in humans remains a challenging task in genomics studies. Recent advances in sequencing technologies mean there are now thousands of sequenced human genomes, revealing millions of single nucleotide variants (SNVs). For non-synonymous SNVs present in pr...
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| Huvudupphovsmän: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Oxford University Press
2014
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4086131/ https://ncbi.nlm.nih.gov/pubmed/24906884 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gku483 |
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