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Laundering CNV data for candidate process prioritization in brain disorders
BACKGROUND: Prioritization of genomic data has become a useful tool for uncovering the phenotypic effect of genetic variations (e.g. copy number variations or CNV) and disease mechanisms. Due to the complexity, brain disorders represent a major focus of genomic research aimed at revealing pathologic...
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| Udgivet i: | Mol Cytogenet |
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| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2019
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6933640/ https://ncbi.nlm.nih.gov/pubmed/31890034 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-019-0468-7 |
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