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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...
Uloženo v:
| Vydáno v: | Mol Cytogenet |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2019
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| Témata: | |
| On-line přístup: | 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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